The intramitochondrial dynamin-related GTPase Mgm1p is a component of a protein complex that mediates mitochondrial fusion
Section of Molecular and Cellular Biology, University of California, Davis, Davis, California, 95616|, http://www.100md.com
Abstract|, http://www.100md.com
Abalance between fission and fusion events determines the morphology of mitochondria. In yeast, mitochondrial fission is regulated by the outer membrane–associated dynamin-related GTPase, Dnm1p. Mitochondrial fusion requires two integral outer membrane components, Fzo1p and Ugo1p. Interestingly, mutations in a second mitochondrial-associated dynamin-related GTPase, Mgm1p, produce similar phenotypes to fzo1 and ugo cells. Specifically, mutations in MGM1 cause mitochondrial fragmentation and a loss of mitochondrial DNA that are suppressed by abolishing DNM1-dependent fission. In contrast to fzo1ts mutants, blocking DNM1-dependent fission restores mitochondrial fusion in mgm1ts cells during mating. Here we show that blocking DNM1-dependent fission in mgm1 cells fails to restore mitochondrial fusion during mating. To examine the role of Mgm1p in mitochondrial fusion, we looked for molecular interactions with known fusion components. Immunoprecipitation experiments revealed that Mgm1p is associated with both Ugo1p and Fzo1p in mitochondria, and that Ugo1p and Fzo1p also are associated with each other. In addition, genetic analysis of specific mgm1 alleles indicates that Mgm1p's GTPase and GTPase effector domains are required for its ability to promote mitochondrial fusion and that Mgm1p self-interacts, suggesting that it functions in fusion as a self-assembling GTPase. Mgm1p's localization within mitochondria has been controversial. Using protease protection and immuno-EM, we have shown previously that Mgm1p localizes to the intermembrane space, associated with the inner membrane. To further test our conclusions, we have used a novel method using the tobacco etch virus protease and confirm that Mgm1p is present in the intermembrane space compartment in vivo. Taken together, these data suggest a model where Mgm1p functions in fusion to remodel the inner membrane and to connect the inner membrane to the outer membrane via its interactions with Ugo1p and Fzo1p, thereby helping to coordinate the behavior of the four mitochondrial membranes during fusion.
Key Words: mitochondria; intermembrane space; membranes; fusion; dynamin-related GTPase5i}}*r, 百拇医药
Introduction5i}}*r, 百拇医药
Mitochondria are complex organelles bound by both an inner and an outer membrane. In Saccharomyces cerevisiae, mitochondria form branched, reticular structures via a mechanism dependent on both fission and fusion events . Fission is mediated by the coordinated actions of three proteins: Dnm1p, a dynamin-related GTPase; Mdv1p, a WD domain protein; and Fis1p, a small integral outer membrane protein . Current data suggest that Dnm1p is localized to punctate structures that are targeted to the outer mitochondrial membrane by Fis1p where it mediates fission in an Mdv1p- and Fis1p-dependent manner5i}}*r, 百拇医药
In contrast to mitochondrial fission, the mechanism whereby the outer and inner mitochondrial membranes are coordinately fused is less clear. Until recently, the only known component involved in mitochondrial fusion was Fzo1p, a novel GTPase with homologues in Drosophila melanogaster and humans . In S. cerevisiae, mutations in, or deletion of, FZO1 cause mitochondria to fragment, a phenotype consistent with a block in fusion. Based on kinetic analysis, mitochondrial DNA (mtDNA) loss is thought to be a secondary consequence of mitochondrial fragmentation in fzo mutants . Interestingly, disruption of fission in fzo1 mutants suppresses mitochondrial fragmentation and restores mitochondrial tubules, but does not restore mitochondrial fusion during mating, indicating that FZO1 plays a direct role in this process
Recently, two genes, named UGO1 and UGO2, were identified in a genetic screen for mutations that caused DNM1-dependent loss of mitochondrial DNA and were shown to be required for mitochondrial fusion during mating . To date, the sequence of the UGO2 gene has not been reported. However, UGO1 encodes a 58-kD integral outer mitochondrial membrane protein with its NH2 terminus in the cytosol and its COOH terminus in the intermembrane space. In a manner identical to fzo1 mutants, ugo mutants have fragmented mitochondria and lose mtDNA during cell division. Disruption of fission in a ugo1 background restores mitochondrial tubules, but not mitochondrial fusion, consistent with a direct role in mitochondrial fusion . Interestingly, localization of Ugo1p's domains in both the cytosol and the intermembrane space suggests that it could interact with components both inside and outside of the organelle.'y?#&, http://www.100md.com
Mutations in MGM1, a dynamin-related GTPase, also were found to cause fragmentation and aggregation of mitochondria with secondary loss of mtDNA, raising the possibility that MGM1 might function in fusion . In addition, mitochondrial fragmentation and mtDNA loss in mgm1 mutants are suppressed when fission is abolished by deletion of DNM1 . However, in contrast to fzo1ts cells, deletion of DNM1 in mgm1ts cells restores mitochondrial fusion during mating. This observation suggests that MGM1 may not be directly involved in fusion
Structural Mgm1p homologues have been identified in higher eukaryotes, where they also have been shown to regulate mitochondrial morphology and function . Interestingly, the human homologue of Mgm1p, OPA1, was shown to be mutated in individuals with autosomal dominant optic atrophy, indicating the important role that mitochondrial structure plays in cellular function . The reported submitochondrial localization of Mgm1p homologues, however, has been conflicting. Data from both protease protection and immuno-EM analyses indicate that Mgm1p is localized to the intermembrane space, associated with the inner mitochondrial membrane. A previous study reported an outer membrane localization of Mgm1p , and the Schizosaccharomyces pombe homologue, Msp1p, was reported to be localized to the mitochondrial matrix, associated with the inner membrane . Recently, however, OPA1 was reported to reside in the mitochondrial intermembrane space, associated with the inner membrane, in agreement with findings on Mgm1p's localization by
In this report, we show that blocking DNM1-dependent fission in mgm1 cells does not restore mitochondrial fusion during mating. This observation is in contrast to our previous results where fusion was observed during mating in mgm1ts dnm1 cells . To address whether Mgm1p plays a direct role in fusion, we have performed cytological, biochemical, and genetic analyses. We show that Mgm1p is in a complex with two mitochondrial fusion components that reside in the outer membrane, Ugo1p and Fzo1p, and that its GTPase and assembly activities are required for mitochondrial fusion. Taken together, our data suggest a model where Mgm1p functions to remodel inner membranes and, through its association with outer membrane components, coordinates the behavior of the inner and outer membranes during fusion.2rt%:), http://www.100md.com
Results and discussion2rt%:), http://www.100md.com
MGM1 is required for mitochondrial fusion2rt%:), http://www.100md.com
Deletion of, or mutations in, MGM1 causes mitochondrial fragmentation and a subsequent loss of mitochondrial DNA in a similar fashion to mutations in FZO1 or UGO1, two genes required for mitochondrial fusion . We previously reported that mgm1 mutants also failed to fuse during mating, suggesting that MGM1 plays a role in fusion . We asked if this block in fusion was due to structural limitations of fragments, or whether MGM1 plays a direct role in fusion by deleting the dynamin-related GTPase DNM1 to disrupt fission in mgm1 mutants. We found that deletion of DNM1 in mgm1ts mutants blocked mitochondrial fragmentation and restored mitochondrial tubules, in an identical fashion to fzo1 and ugo1 mutants. Restoration of mitochondrial tubules in mgm1ts cells, as assessed by mitochondrial morphology and growth, was accompanied by restored mitochondrial fusion unpublished data). This is in contrast to fzo1-1 dnm1 mutants, where mitochondrial tubules are restored, but mitochondrial fusion is blocked
In the present study, we assayed for mitochondrial fusion in mgm1dnm1 cells during mating. As shown in , we observed that, as expected, mitochondrial fragmentation due to loss of MGM1 function was suppressed by blocking DNM1-dependent fission, and tubules were restored (E–H). However, in contrast to wild-type and mgm1tsdnm1 cells , mitochondrial fusion was blocked in mgm1dnm1 cells (, E–H, 8% unfused, n = 50; I–L, 98% unfused, n = 50), a phenotype identical to that observed for fzo1dnm1 cells (, N–P). One explanation for this observed difference between mgm1 and mgm1ts strains is that the mgm1ts alleles tested are hypomorphs and, when shifted to the nonpermissive temperature, retain enough function to support mitochondrial fusion. In this case, Mgm1p may be essential for mitochondrial fusion, and our observations indicate that the requirement for Mgm1p function in fusion is diminished in the context of mitochondrial tubules, as opposed to mitochondrial fragments. Alternatively, it is possible that mitochondrial fusion is abolished in mgm1dnm1 cells as a secondary, indirect consequence of loss of MGM1 function.
fig.ommtted:0z\/7c, http://www.100md.com
MGM1 is required for mitochondrial fusion during mating. Cells of the opposite mating type expressing either mito–GFP or mito–RFP were grown to log phase at 25°C, mated at 37°C, and imaged as previously described . Mitochondrial fusion was assessed by examining merged mito–GFP and mito–RFP images of large-budded homozygous zygotes formed from wild type (A–D), mgm1–5dnm1 (E–H), mgm1dnm1 (I–L), and fzo1dnm1 (M–P). Bars, 2 µm.:0z\/7c, http://www.100md.com
fig.ommtted:0z\/7c, http://www.100md.com
Mgm1p, Ugo1p, and Fzo1p interact. (A) Immunoprecipitations were performed using anti-HA on cross-linked mitochondrial fractions isolated from MGM1:3XHA (lanes 1 and 2), UGO1:3XHA (lanes 3 and 4), wild-type (lanes 5 and 6), and mgm1 UGO1:3XHA (lanes 7 and 8) strains. The total and immunoprecipitated pellet fractions were probed with antibodies as described in the Materials and methods. The amount loaded from the total fraction is equivalent to 2.5% of the bound fraction. (B) Mitochondrial extracts from UGO1:3XHA (lanes 1 and 2), mgm1 UGO1:3XHA (lanes 3 and 4), and fzo1 UGO1:3XHA (lanes 5 and 6) were immunoprecipitated using anti-Mgm1 antibodies. The total and pellet fractions were analyzed by Western blotting with anti-HA. Ugo1:3XHAp is designated Ugo1HA in the figure.
Mgm1p, Ugo1p, and Fzo1p interact;*p46, 百拇医药
To examine these two possibilities, we tested the relationship of Mgm1p to two known fusion components, Ugo1p and Fzo1p, by performing immunoprecipitation reactions. Immunoprecipitations were performed on mitochondrial-enriched fractions isolated from wild-type cells or cells expressing either a previously characterized and functional internally HA-tagged version of Mgm1p (Mgm1:3XHAp) or a functional COOH-terminal HA epitope–tagged allele of Ugo1p (Ugo1:3XHAp) using both mouse monoclonal anti-HA antibodies and polyclonal anti-Mgm1 antibodies . We were unable to detect interactions among Mgm1p, Fzo1p, and Ugo1p in native cell extracts, suggesting that they might be labile in vitro. To overcome this instability, before immunoprecipitation, proteins were cross-linked in mitochondrial fractions with the bifunctional, reversible cross-linker dithiobis-(succinimidyl propionate) (DSP) and extracted under denaturing conditions. After immunoprecipitation, cross-links were reversed with reducing agents and precipitates were analyzed by SDS-PAGE and Western blotting.
We first examined whether Mgm1p and Ugo1p interact with Fzo1p by performing immunoprecipitations using anti-HA antibodies from cross-linked Mgm1:3XHA-tagged and Ugo1:3XHA-tagged mitochondrial extracts. Western blot analysis with anti-Fzo1p antibodies of fractions from mitochondrial extracts immunoprecipitated with anti-HA antibodies demonstrated that a fraction of Fzo1p was reproducibly coimmunoprecipitated with either Mgm1p or Ugo1p ( A, lanes 1–4). As expected, the majority of Ugo1:3xHA and Mgm1:3XHA were specifically recovered in immunoprecipitate fractions from cells that expressed these proteins (unpublished data). In contrast, neither the outer mitochondrial membrane fission component, Fis1p, nor the inner membrane protein import component, Tim44p, was observed in the immunoprecipitate fraction, indicating that the interaction of Ugo1p and Mgm1p with Fzo1p is specific ( A, lanes 1–4). In addition, Tim23p, an inner membrane import component that contains an intermembrane space domain, also was not recovered in the immunoprecipitate (unpublished data). To further address specificity, immunoprecipitations were performed from enriched, DSP–cross-linked mitochondrial fractions isolated from wild-type cells, not expressing either Ugo1:3XHA or Mgm1:3XHA. Under these conditions, Fzo1p was not recovered in the immunoprecipitate fraction, indicating that the coimmunoprecipitation of Fzo1p with the anti-HA antibody is dependent on the HA-tagged versions of Ugo1p and Mgm1p ( A, lanes 5 and 6).
To further examine the nature of Ugo1p's interactions with Fzo1p, immunoprecipitation experiments were performed using a DSP–cross-linked mitochondrial fraction isolated from mgm1 Ugo1HA cells. Interestingly, Western blot analysis of fractions from anti-HA immunoprecipitations in mgm1 Ugo1:3XHA mitochondria revealed that although Fzo1p was present at lower levels, it coimmunoprecipitated with anti-HA antibodies, indicating that an Fzo1p–Ugo1p interaction occurs independently of Mgm1p ( A, lanes 7 and 8). Interestingly, the level of Fzo1p in total mgm1 Ugo1:3XHA yeast extracts prepared under denaturing conditions was similar to that observed in wild-type Ugo1:3XHA extracts (unpublished data). Thus, Fzo1p's instability in the mitochondrial fraction from mgm1 Ugo1:3XHA cells probably results from proteolysis in vitro. These observations suggest that in the absence of Mgm1p, Fzo1p may be present in mitochondrial membranes in an altered conformation, consistent with our observation of an Fzo1p–Mgm1p interaction.
Our observations indicate that both Mgm1p and Ugo1p are present in a complex(es) with Fzo1p. To determine whether Mgm1p also is present in a complex containing Ugo1p, we performed immunoprecipitations using anti-Mgm1p antibodies from cross-linked Ugo1:3XHA-tagged mitochondria. Significantly, we observed that a fraction of Ugo1p was specifically and reproducibly coimmunoprecipitated with Mgm1p ( B, lanes 1–4). Interestingly, Ugo1p coimmunoprecipitated with Mgm1p in the absence of Fzo1p, indicating that the interaction observed between Mgm1p and Ugo1p occurs independently of Fzo1p ( B, lanes 5 and 6). Taken together, these biochemical data demonstrate that Mgm1p forms a complex(es) with two known fusion components, Ugo1p and Fzo1p, and support a direct role for Mgm1p in mitochondrial fusion.e;d{1, 百拇医药
Mgm1p behaves as a dynamin-related GTPasee;d{1, 百拇医药
In addition to a GTPase domain, dynamin-related GTPases share a middle domain and an assembly or GTPase effector domain (GED) . These additional domains function together with the GTPase domain to promote the self-assembly of dynamin-related GTPases into ring and spiral-like structures, resulting in a stimulation of GTPase activity Both the self-assembly and GTPase activities of dynamin-related GTPases have been shown to be important for their ability to remodel biological membranes . To further characterize Mgm1p's role in fusion, we examined whether mutations predicted to affect the GTPase and self-assembly activities of Mgm1p would affect its ability to promote mitochondrial fusion.
We created mutants predicted to be defective in the GTPase cycle, based on the analysis of dynamin and other GTPase superfamily members, by mutating specific conserved residues in the G1 and G2 nucleotide binding regions of Mgm1p. Conserved residues in the G1 region, K223 and S224, and in the G2 region, T244, were mutated to alanine in Mgm1p. We first examined the expression of these mutant forms of Mgm1p in mgm1 cells by Western blotting. Interestingly, only Mgm1S224A and Mgm1T244A were detected in cells, suggesting that the nucleotide binding state of Mgm1p affects its stability in vivo (; unpublished data).7t, 百拇医药
fig.ommtted7t, 百拇医药
Determination of the steady-state levels of mutant Mgm1 proteins. JNY845 was transformed with pRS425 vectors containing mgm1 mutants, and strains were grown overnight to log phase. Whole cell extracts were made and analyzed by SDS-PAGE followed by Western blotting as described in the Materials and methods. Western analysis of the cytosolic protein 3-phosphoglycerokinase (PGK) was used as a loading control.
Mutations of S224 in the G1 region of Mgm1p are predicted to alter nucleotide binding, and mutations in T244 in the G2 region of Mgm1p are predicted to stabilize the protein in the GTP-bound form . Recently, however, a careful analysis of the effects of similar mutations on dynamin's ability to bind and hydrolyze GTP revealed that they did not produce the predicted effects and instead destabilized the binding of both GDP and GTP to mutant proteins . Nevertheless, we determined the ability of these Mgm1 mutant proteins to complement both the mitochondrial morphology and fusion defects in mgm1 cells.)!, 百拇医药
Both the S224A and T244A Mgm1p mutants were unable to support wild-type levels of Mgm1p function . Specifically, these mutants were unable to fully complement the mitochondrial morphology defect of mgm1 cells and also failed to completely restore the ability of mitochondria to fuse during mating in mgm1dnm1 cells, where mitochondrial tubules were restored. Interestingly, when Mgm1S224A and Mgm1T224A were overexpressed in wild-type cells, they interfered to varying degrees and in a dose-dependent manner with wild-type MGM1 function, as assessed by mitochondrial morphology, similar to observations of dynamin and Dnm1p mutants . These observations are consistent with a previous study reporting that Mgm1S224Np failed to complement the mitochondrial morphology defect in mgm1 cells and displayed a dominant negative phenotype when overexpressed in wild-type cells . We conclude that Mgm1p's GTPase cycle is essential for its ability to function in mitochondrial fusion.
fig.ommttedm, 百拇医药
Mutations in Mgm1p's GTPase and GTPase effector domains affect mitochondrial morphology and fusionm, 百拇医药
fig.ommttedm, 百拇医药
Mutations in Mgm1p's GTPase and GTPase effector domains cause dose-dependent dominant negative effects on mitochondrial morphologym, 百拇医药
Intermolecular interactions are required for dynamin and dynamin-related GTPases to function (for review see ). Our observation that overexpression of Mgm1p GTPase mutants induced mitochondrial fragmentation in wild-type cells is consistent with the possibility that mutant Mgm1p coassembles and interferes with the function of wild-type Mgm1p and suggests that Mgm1p self-assembly is required for its function in fusion. To further test this, we examined the role of Mgm1p's putative GED in mitochondrial fusion. Lysine and arginine residues in dynamin's GED have been shown previously to play a role in assembly and assembly-stimulated GTPase activity To test the role of these basic residues, we mutated all of the arginine and lysine residues in Mgm1p's predicted GED to alanine and assessed the function of these mutant proteins by examining mitochondrial morphology and fusion in cells. Interestingly, two mutations in MGM1's predicted GED domain, R824A and K854A, failed to completely restore mitochondrial morphology in mgm1 cells and mitochondrial fusion during mating in mgm1dnm1 cells . Western blot analysis of cells showed that these mutant proteins were expressed at levels comparable to wild-type Mgm1p, indicating that loss of function was not the result of protein instability. In the case of Mgm1S224A and Mgm1K854A mutants, the defect observed in mitochondrial fusion in mgm1nm1 cells was less severe than that observed for mitochondrial morphology in mgm1 cells. This discrepancy could be explained if the requirement for Mgm1p function in fusion is diminished in the context of mitochondrial tubules, as opposed to mitochondrial fragments, which also may explain our previous observations for mgm1ts cells . Similar to Mgm1p GTPase mutants, when Mgm1R824A and Mgm1K854A were overexpressed in wild-type cells, they interfered to varying degrees and in a dose-dependent manner with wild-type MGM1 function, as assessed by mitochondrial morphology . These observations indicate that Mgm1p's GED is important for its function and suggest that Mgm1p self-assembly occurs and is important for the ability of Mgm1p to facilitate mitochondrial fusion.
To further test whether Mgm1p self-assembles in vivo, we analyzed diploids from crosses of several mgm1ts mutants, previously isolated in a forward genetic screen for mutants unable to maintain mtDNA at elevated temperatures . We reasoned that if Mgm1p self-interacts, two different mutations in MGM1 may be able to compensate for one another within an assembled Mgm1p complex and restore mitochondrial fusion activity, resulting in maintenance of mtDNA and growth on a nonfermentable carbon source at the nonpermissive temperature. Interestingly, the entire collection of mgm1ts mutants isolated in the screen contained mutations only in either the GTPase domain or the GED, underscoring the importance of these domains in MGM1 function ( A; unpublished data). A combination of a subset of these mgm1ts alleles in diploids grew at the nonpermissive temperature on media containing glycerol, indicating that they displayed intragenic complementation . In total, data from our genetic analysis of mgm1 mutants support a model where Mgm1p functions in fusion as a self-assembling GTPase.
fig.ommttedlwwu!2, http://www.100md.com
Intragenic complementation is observed between mgm1 temperature-sensitive mutants. (A) Schematic of MGM1 domain structure designating the position of the temperature-sensitive mutations analyzed for intragenic complementation is shown. (B) Analysis of intragenic complementation of mgm1ts alleles. Growth on glycerol is indicated by +.lwwu!2, http://www.100md.com
Mgm1p is an intermembrane space proteinlwwu!2, http://www.100md.com
We previously reported that Mgm1p is an intermembrane space protein based on data from protease protection experiments of intact and hypo-osmotically shocked mitochondria. Protease protection experiments, however, are technically difficult in that isolated mitochondria must be intact and hypo-osmotic conditions for selectively disrupting the outer mitochondrial membrane are variable. Because of these difficulties, and the reported differing submitochondrial localizations of Mgm1p and its S. pombe orthologue, Msp1p, we reexamined Mgm1p's submitochondrial localization using a novel method involving the tobacco etch virus (TEV) protease.
Tobacco etch virus has a 27-kD protease subunit that specifically cleaves proteins containing the consensus sequence EXXYXQØS, which is absent from all predicted ORFs from the yeast genome . For this reason, it has been used successfully to examine the in vivo topology of proteins. We obtained plasmids harboring genes encoding active mitochondrial matrix (matrix-TEV)– and intermembrane space (IMS-TEV)–targeted versions of TEV, constructed using the well-defined targeting sequences of ATP9 and CYB2, respectively (Thatcher, J., and J. Shaw, personal communication).88rvyp?, http://www.100md.com
To determine the localization of Mgm1p in vivo, MGM1:3XHA, contained on a CEN/ARS plasmid, was engineered with a sequence encoding a TEV consensus cleavage site directly preceding the coding sequence of the 3XHA tag (MGM1:tev:3XHA). Interestingly, this version of MGM1 maintained function, as assessed by its ability to support the growth of {Delta} mgm1 cells on media containing a nonfermentable carbon source (unpublished data). Given the internal position of the TEV cleavage site and the 3XHA tag, cleavage of Mgm1:tev:3XHAp by TEV is predicted to produce a product of ~
75 kD, specifically detected by Western analysis using anti-HA antibodies.nq/ns(, 百拇医药
Western blot analysis of mitochondrial fractions isolated from wild-type cells expressing Mgm1:tev:3XHAp alone with anti-HA antibodies revealed two predominant forms of Mgm1:tev:3XHAp, as seen previously in cells expressing both Mgm1:3XHAp and native, untagged Mgm1p (, lane 1). When coexpressed with matrix-TEV, the two Mgm1:tev:3XHAp products remained unchanged (, lane 2). In contrast, an additional, faster-migrating species, estimated at 75 kD, was detected with anti-HA antibodies in cells coexpressing Mgm1:tev:3XHAp and IMS-TEV (, lane 3, asterisk). The apparent molecular mass of this species is in agreement with the size of a predicted TEV-dependent cleavage product of Mgm1:tev:3XHAp and indicates that Mgm1p was accessible only to the IMS-targeted version of TEV. This observation confirms our previously published results that Mgm1p is localized to the intermembrane space and is in agreement with the recently published localization of the human Mgm1p orthologue, OPA1
fig.ommtted44!-0, 百拇医药
Mgm1p is in the IMS compartment in vivo. Mitochondria were isolated from strains expressing Mgm1:tev:3XHAp alone (lane 1), Mgm1:tev:3XHAp and ATP9-TEVp (lane 2), and Mgm1:tev:3XHAp and CYB2-TEVp (lane 3) and analyzed by SDS-PAGE followed by Western blotting with anti-HA and anti-porin antibodies, as a loading control. Asterisk indicates a TEV-specific Mgm1 cleavage product.44!-0, 百拇医药
Our previous immuno-EM observations of Mgm1p indicate that it is associated with the mitochondrial inner membrane . Since our report, additional observations have been made that substantiate this conclusion. In a study that revealed a role for ATP synthase in the formation of mitochondrial inner membrane cristae structures in yeast, the localization of the outer membrane protein porin and the inner membrane–associated ß subunit of ATP synthase were determined by immuno-EM In the case of the ß subunit of ATP synthase, gold particles were observed in the interior of mitochondria, in most cases clearly associated with cristae, similar to the pattern we observed for Mgm1p. In contrast, in the case of porin, the majority of gold particles were associated with the periphery of mitochondria, consistent with an outer membrane localization . In addition, immuno-EM localization of OPA1 indicates that it is localized within mitochondria, associated with cristae membranes, in a pattern similar to that observed for Mgm1p . Thus, taken together, these observations substantiate our previous report of Mgm1p topology, where it is tightly associated with the inner membrane, with its GTPase domain localized to the intermembrane space compartment
A model for Mgm1p function during mitochondrial fusion]k\l, 百拇医药
The data presented in this paper support a model where the intermembrane space protein Mgm1p functions in fusion as a self-assembling GTPase and plays a role in coordinating the inner and outer membranes during the fusion process. As a self-assembling GTPase, Mgm1p may directly promote the fusion of the inner membrane by helping to form a transient tubule or protrusion of this membrane, similar to the role proposed for the dynamin-related GTPase phragmoplastin in cell plate formation in plants . This Mgm1p-dependent inner membrane remodeling event may be regulated by fusion-promoting events in the outer membrane via Mgm1p's interaction with Ugo1p and Fzo1p. In addition, Mgm1p's interactions with Ugo1p and Fzo1p may serve to physically coordinate the behavior of both membranes and promote the formation of a double membrane structure with a higher radius of curvature, thereby producing a fusion-competent microenvironment. Alternatively, Mgm1p might function as a classical GTPase that recruits Fzo1p and Ugo1p, which in turn promote fusion, similar to the role proposed for dynamin during endocytosis. Recently it was reported that deletion of several novel ORFs encoding predicted inner mitochondrial membrane proteins caused mitochondrial fragmentation and mtDNA loss in cells, similarly to fzo1, ugo, and mgm1 mutants . Given their predicted localization and mutant phenotypes, it is attractive to speculate that these components may play a role in mitochondrial fusion by modulating Mgm1p function. Elucidating the exact role of these components in mitochondrial morphology will help illuminate the complex process of coordinately fusing four mitochondrial membranes.
Materials and methodss.!|'\, http://www.100md.com
Plasmid and strain construction and analysiss.!|'\, http://www.100md.com
Strains used in this study are summarized in . Temperature-sensitive MGM1 alleles were isolated in a previous screen and mutations were identified by amplifying the MGM1 locus in mutant cells by PCR using Vent polymerase and sequencing the products directly (Davis Sequencing, University of California, Davis). To mutagenize MGM1, XbaI sites flanking the MGM1 locus with its native promoter were engineered by PCR. The entire locus was subcloned into pRS425 or pRS315 . Point mutations in MGM1 were created using a QuikChange mutagenesis kit. Mutations were confirmed by sequence analysis of the entire MGM1 insert (DBS sequencing facility, Section of Molecular and Cellular Biology, University of California, Davis). A yeast strain harboring a COOH-terminal 3XHA–tagged version of Ugo1p was created by homologous recombination between the UGO1 locus in JSY1826 cells and a PCR product as previously described . This strain, JNY894, was confirmed by PCR of the UGO1 locus and Western blotting using anti-HA antibodies (Covance Research). Strains JNY898 and JNY903 were obtained by crossing, sporulation, and tetrad analysis. To construct a TEV cleavage site within Mgm1p, XbaI sites flanking MGM1:3XHA with its native promoter were engineered by PCR from genomic JSY2519 DNA. The XhoI to EcoRI and NotI to SalI restriction sites were destroyed in pRS313 to create pEDI14. MGM1:3XHA was nondirectionally cloned into pEDI14 using the engineered XbaI sites. A TEV protease site was created by annealing complementary oligonucleotide primers to the following sequence: TCG ACG AAA ACT TGT ATT TTC AAG GTG and TCG ACA CCT TGA AAA TAC AAG TTT TCG. This TEV site was inserted into a unique XhoI site preceding the sequence encoding 3XHA in MGM1:3XHA, destroying the XhoI site and creating MGM1p:tev:3XHA. Whole cell extracts were prepared as previously described . Mitochondrial morphology and mitochondrial fusion during mating were analyzed as previously described
fig.ommtted/:1tn, 百拇医药
Strains used in this study/:1tn, 百拇医药
Immunoprecipitation of cross-linked mitochondrial proteins/:1tn, 百拇医药
To enrich for mitochondrial proteins, mitochondria were isolated by differential centrifugation as previously described , except that the mitochondrial fraction was pelleted only once. The mitochondrial-enriched membrane fraction resulting from 100 OD600 of spheroplasts was resuspended in 500 µl mitochondrial isolation buffer (20 mM Hepes, pH 7.5, 600 mM sorbitol, and 1x protease inhibitors). To cross-link associated proteins, DSP was added to a final concentration of 1 mM and incubated at 0°C for 2 h. Cross-linking was stopped by the addition of 100 mM glycine, pH 8.0, followed by precipitation of proteins using trichloroactetic acid (final concentration 10% wt/vol). Mitochondrial proteins were denatured and solubilized by suspension in 100 µl MURB (100 mM MES, pH 7, 1% SDS, 3 M urea) and incubated at 65°C for 5 min, followed by the addition of 750 µl TWIP (50 mM Tris-Cl, pH 7.5, 150 mM NaCl, 0.5% Tween 20, 0.1% EDTA). The supernatant fraction was incubated overnight at 4°C with 75 µl protein A agarose beads with gentle rocking. Protein A agarose beads were washed three times with 1 ml TWIP. Bead pellets were resuspended in MURB with 5% ß-mercaptoethanol and incubated at 65°C for 10 min to release proteins into the sample buffer and reduce cross-links. Protein in total and protein A agarose–bound fractions were analyzed by SDS-PAGE followed by Western blot analysis.
In vivo localization of Mgm1p(6g3%, 百拇医药
GAL1-regulated matrix and IMS-targeted versions of TEV protease were were provided by J. Thatcher and J. Shaw (University of Utah, Salt Lake City, UT). Plasmids were cotransformed into strains with MGM1:tev:3XHAp and cells were grown to log phase in selective media containing raffinose. TEV expression was induced by subculturing cells in media containing galactose, and proteolysis of Mgm1:tev:3XHAp by TEV protease was determined by the analysis of mitochondria-enriched fractions after growth in galactose-containing media for 30 min using SDS-PAGE and Western blotting.(6g3%, 百拇医药
SDS-Page and Western blot analysis(6g3%, 百拇医药
All protein samples were analyzed by gel electrophoresis using 12.5% Anderson polyacrylamide gels as previously described . Proteins were transferred to a nitrocellulose membrane and analyzed using primary antibodies to Tim44p (1:1,000; Debukmar Pain), anti-Fis1p (1:2,000), Mgm1p (1:200), HA (1:2,500; Covance), 3-phosphoglycerokinase (PGK) (1:1,000; Molecular Probes, Inc.), GFP (1:10,000; Covance), and Fzo1p (1:1,000; provided by J. Shaw) in PBS-T plus 5% dry milk. Rabbit polyclonal anti-Mgm1p antibodies were raised against bacterial-expressed Mgm1p region (amino acids 490–902) from pET28aMGM1490–902 (Covance). Proteins were visualized by incubation with the appropriate secondary antibody conjugated to horseradish peroxidase (1:5,000) in PBS-T plus 5% dry milk, followed by ECL
Acknowledgments$mu#, 百拇医药
We are grateful to John Thatcher and Janet Shaw for providing TEV reagents prior to publication. We are also grateful to members of the Nunnari lab for their critical input into this project.$mu#, 百拇医药
This work was supported by National Science Foundation REU grant to J. Nunnari.$mu#, 百拇医药
Submitted: 3 September 2002$mu#, 百拇医药
Revised: 19 December 2002$mu#, 百拇医药
Accepted: 20 December 2002$mu#, 百拇医药
References$mu#, 百拇医药
Alexander, C., M. Votruba, U.E.A. Pesch, D.L. Thiselton, S. Mayer, A. Moore, M. Rodriguez, U. Kellner, B. Leo-Kottler, G. Auburger, et al. 2000. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nat. Genet. 26:211–215.$mu#, 百拇医药
Bleazard, W., J.M. McCaffery, E.J. King, S. Bale, A. Mozdy, Q. Tieu, J. Nunnari, and J.M. Shaw. 1999. The dynamin-related GTPase Dnm1 regulates mitochondrial fission in yeast. Nat. Cell Biol. 1:298–304.
Bourne, H.R., D.A. Sanders, and F. McCormick. 1991. The GTPase superfamily: conserved structure and molecular mechanism. Nature. 349:117–127.)y@s, 百拇医药
Cerveny, K.L., J.M. McCaffery, and R.E. Jensen. 2001. Division of mitochondria requires a novel DNM1-interacting protein, Net2p. Mol. Biol. Cell. 12:309–321.)y@s, 百拇医药
Chernomordik, L.V., and J. Zimmerberg. 1995. Bending membranes to the task: structural intermediates in bilayer fusion. Curr. Opin. Struct. Biol. 5:541–547.)y@s, 百拇医药
Christianson, T.W., R.S. Sikorski, M. Dante, J.H. Shero, and P. Hieter. 1992. Multifunctional yeast high-copy-number vectors. Gene. 110:119–122.)y@s, 百拇医药
Damke, H., T. Baba, D.E. Warnock, and S.L. Schmid. 1994. Induction of mutant dynamin specifically blocks endocytic coated vesicle formation. J. Cell Biol. 127:915–934.)y@s, 百拇医药
Damke, H., D.D. Binns, H. Ueda, S.L. Schmid, and T. Baba. 2001. Dynamin GTPase domain mutants block endocytic vesicle formation at morphologically distinct stages. Mol. Biol. Cell. 12:2578–2589.)y@s, 百拇医药
Delettre, C., G. Lenaers, J.-M. Griffoin, N. Gigarel, C. Lorenzo, P. Belenguer, L. Pelloquin, J. Grosgeorge, C. Turc-Carel, E. Perret, et al. 2000. Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy. Nat. Genet. 26:207–210.
Dimmer, K.S., S. Fritz, F. Fuchs, M. Messerschmitt, N. Weinbach, W. Neupert, and B. Westermann. 2002. Genetic basis of mitochondrial function and morphology in Saccharomyces cerevisiae. Mol. Biol. Cell. 13:847–853.2, 百拇医药
Faber, K.N., A.M. Kram, M. Ehrmann, and M. Veenhuis. 2001. A novel method to determine the topology of peroxisomal membrane proteins in vivo using the tobacco etch virus protease. J. Biol. Chem. 276:36501–36507.2, 百拇医药
Fekkes, P., K.A. Shepard, and M.P. Yaffe. 2000. Gag3p, an outer membrane protein required for fission of mitochondrial tubules. J. Cell Biol. 151:333–340.2, 百拇医药
Hales, K.G., and M.T. Fuller. 1997. Developmentally regulated mitochondrial fusion mediated by a conserved, novel, predicted GTPase. Cell. 90:121–129.2, 百拇医药
Hermann, G.J., J.W. Thatcher, J.P. Mills, K.G. Hales, M.T. Fuller, J. Nunnari, and J.M. Shaw. 1998. Mitochondrial fusion in yeast requires the transmembrane GTPase Fzo1p. J. Cell Biol. 143:359–374.2, 百拇医药
Hinshaw, J.E. 2000. Dynamin and its role in membrane fission. Annu. Rev. Cell Dev. Biol. 16:483–519.
Hinshaw, J.E., and S.L. Schmid. 1995. Dynamin self-assembles into rings suggesting a mechanism for coated vesicle budding. Nature. 374:190–192.^v+[$#o, 百拇医药
Longtine, M., A. McKenzie, D. Demarini, N. Shah, A. Wach, A. Brachat, P. Philippsen, and J. Pringle. 1998. Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae. Yeast. 14:953–961.^v+[$#o, 百拇医药
Meeusen, S., Q. Tieu, E. Wong, E. Weiss, D. Schieltz, J.R. Yates, and J. Nunnari. 1999. Mgm101p is a novel component of the mitochondrial nucleoid that binds DNA and is required for the repair of oxidatively damaged mitochondrial DNA. J. Cell Biol. 145:291–304.^v+[$#o, 百拇医药
Misaka, T., T. Miyashita, and Y. Kubo. 2002. Primary structure of a dynamin-related mouse mitochondrial GTPase and its distribution in brain, subcellular localization, and effect on mitochondrial morphology. J. Biol. Chem. 277:15834–15842.^v+[$#o, 百拇医药
Mozdy, A.D., J.M. McCaffery, and J.M. Shaw. 2000. Dnm1p GTPase-mediated mitochondrial fission is a multi-step process requiring the novel integral membrane component Fis1p. J. Cell Biol. 151:367–380.
Muhlberg, A.B., D.E. Warnock, and S.L. Schmid. 1997. Domain structure and intramolecular regulation of dynamin GTPase. EMBO J. 16:6676–6683.k, 百拇医药
Nunnari, J., W. Marshall, A. Straight, A. Murray, J.W. Sedat, and P. Walter. 1997. Mitochondrial transmission during mating in S. cerevisiae is determined by mitochondrial fusion and fission and the intramitochondrial segregation of mtDNA. Mol. Biol. Cell. 8:1233–1242.k, 百拇医药
Okamoto, P.M., B. Tripet, J. Litowski, R.S. Hodges, and R.B. Vallee. 1999. Multiple distinct coiled-coils are involved in dynamin self-assembly. J. Biol. Chem. 274:10277–10286.k, 百拇医药
Olichon, A., L.J. Emorine, E. Descoins, L. Pelloquin, L. Brichese, N. Gas, E. Guillou, C. Delettre, A. Valette, C.P. Hamel, et al. 2002. The human dynamin-related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter-membrane space. FEBS Lett. 523:171–176.k, 百拇医药
Otsuga, D., B.R. Keegan, E. Brisch, J.W. Thantcher, G.J. Hermann, W. Bleazard, and J. Shaw. 1998. The dynamin GTPase, Dnm1p, controls mitochondrial morphology in yeast. J. Cell Biol. 143:333–349.
Paumard, P., J. Vaillier, B. Coulary, J. Schaeffer, V. Soubannier, D.M. Mueller, D. Brethes, J.-P. di Rago, and J. Velours. 2002. The ATP synthase is involved in generating mitochondrial cristae morphology. EMBO J. 21:221–230.j$?$!u, 百拇医药
Pelloquin, L., P. Belenguer, Y. Menon, N. Gas, and B. Ducommun. 1999. Fission yeast msp1 is a mitochondrial dynamin-related protein. J. Cell Sci. 112:4151–4161.j$?$!u, 百拇医药
Rapaport, D., M. Brunner, W. Neupert, and B. Westermann. 1998. Fzo1p is a mitochondrial outer membrane protein essential for the biogenesis of functional mitochondria in Saccharomyces cerevisiae. J. Biol. Chem. 273:20150–20155.j$?$!u, 百拇医药
Samuels, A.L., T.H. Giddings, and L.A. Staehelin. 1995. Cytokinesis in tobacco BY-2 and root tip cells: a new model of cell plate formation in higher plants. J. Cell Biol. 130:1345–1357.j$?$!u, 百拇医药
Santel, A., and M.T. Fuller. 2001. Control of mitochondrial morphology by a human mitofusin. J. Cell Sci. 114:867–874.j$?$!u, 百拇医药
Sesaki, H., and R.E. Jensen. 1999. Division versus fusion: Dnm1p and Fzo1p antagonistically regulate mitochondrial shape. J. Cell Biol. 147:699–706.
Sesaki, H., and R.E. Jensen. 2001. UGO1 encodes an outer membrane protein required for mitochondrial fusion. J. Cell Biol. 152:1123–1134..6, http://www.100md.com
Sever, S., A.B. Muhlberg, and S.L. Schmid. 1999. Impairment of dynamin's GAP domain stimulates receptor-mediated endocytosis. Nature. 398:481–486..6, http://www.100md.com
Sever, S., H. Damke, and S.L. Schmid. 2000. Dynamin:GTP controls the formation of constricted coated pits, the rate limiting step in clathrin-mediated endocytosis. J. Cell Biol. 150:1137–1147..6, http://www.100md.com
Shaw, J.M., and J. Nunnari. 2002. Mitochondrial dynamics and division in budding yeast. Trends Cell Biol. 12:178–184..6, http://www.100md.com
Shepard, K., and M. Yaffe. 1999. The yeast dynamin-like protein, Mgm1p, functions on the mitochondrial outer membrane to mediate mitochondrial inheritance. J. Cell Biol. 144:711–719..6, http://www.100md.com
Smirnova, E., D.-L. Shurland, E.D. Newman-Smith, B. Pishvaee, and A.M. van der Bliek. 1999. A model for dynamin self-assembly based on binding between three different protein domains. J. Biol. Chem. 274:14942–14947.
Smith, T.A., and B.D. Kohorn. 1991. Direct selection for sequences encoding proteases of known specificity. Proc. Natl. Acad. Sci. USA. 88:5159–5162.&*8, http://www.100md.com
Tieu, Q., and J. Nunnari. 2000. Mdv1p is a WD repeat protein that interacts with the dynamin-related GTPase, Dnm1p, to trigger mitochondrial division. J. Cell Biol. 151:353–365.&*8, http://www.100md.com
Tieu, Q., V. Okreglak, K. Naylor, and J. Nunnari. 2002. The WD repeat protein, Mdv1p, functions as a molecular adaptor by interacting with Dnm1p and Fis1p during mitochondrial fission. J. Cell Biol. 158:445–452.&*8, http://www.100md.com
van der Bliek, A.M. 1999. Functional diversity in the dynamin family. Trends Cell Biol. 9:96–102.&*8, http://www.100md.com
Verma, D.P., and X. Gu. 1996. Vesicle dynamics during cell-plate formation in plants. Trends Plant Sci. 1:145–149.&*8, http://www.100md.com
Wong, E.D., J.A. Wagner, S.W. Gorsich, J.M. McCaffery, J.M. Shaw, and J. Nunnari. 2000. The dynamin-related GTPase, Mgm1p, is an intermembrane space protein required for maintenance of fusion competent mitochondria. J. Cell Biol. 151:341–352.&*8, http://www.100md.com
Zhang, P., and J.E. Hinshaw. 2001. Three-dimensional reconstruction of dynamin in the constricted state. Nat. Cell Biol. 3:922–926.(Edith D. Wong Jennifer A. Wagner Sidney V. Scott Voytek Okreglak Timothy J. Holewinske Ann Cassidy-S)
Abstract|, http://www.100md.com
Abalance between fission and fusion events determines the morphology of mitochondria. In yeast, mitochondrial fission is regulated by the outer membrane–associated dynamin-related GTPase, Dnm1p. Mitochondrial fusion requires two integral outer membrane components, Fzo1p and Ugo1p. Interestingly, mutations in a second mitochondrial-associated dynamin-related GTPase, Mgm1p, produce similar phenotypes to fzo1 and ugo cells. Specifically, mutations in MGM1 cause mitochondrial fragmentation and a loss of mitochondrial DNA that are suppressed by abolishing DNM1-dependent fission. In contrast to fzo1ts mutants, blocking DNM1-dependent fission restores mitochondrial fusion in mgm1ts cells during mating. Here we show that blocking DNM1-dependent fission in mgm1 cells fails to restore mitochondrial fusion during mating. To examine the role of Mgm1p in mitochondrial fusion, we looked for molecular interactions with known fusion components. Immunoprecipitation experiments revealed that Mgm1p is associated with both Ugo1p and Fzo1p in mitochondria, and that Ugo1p and Fzo1p also are associated with each other. In addition, genetic analysis of specific mgm1 alleles indicates that Mgm1p's GTPase and GTPase effector domains are required for its ability to promote mitochondrial fusion and that Mgm1p self-interacts, suggesting that it functions in fusion as a self-assembling GTPase. Mgm1p's localization within mitochondria has been controversial. Using protease protection and immuno-EM, we have shown previously that Mgm1p localizes to the intermembrane space, associated with the inner membrane. To further test our conclusions, we have used a novel method using the tobacco etch virus protease and confirm that Mgm1p is present in the intermembrane space compartment in vivo. Taken together, these data suggest a model where Mgm1p functions in fusion to remodel the inner membrane and to connect the inner membrane to the outer membrane via its interactions with Ugo1p and Fzo1p, thereby helping to coordinate the behavior of the four mitochondrial membranes during fusion.
Key Words: mitochondria; intermembrane space; membranes; fusion; dynamin-related GTPase5i}}*r, 百拇医药
Introduction5i}}*r, 百拇医药
Mitochondria are complex organelles bound by both an inner and an outer membrane. In Saccharomyces cerevisiae, mitochondria form branched, reticular structures via a mechanism dependent on both fission and fusion events . Fission is mediated by the coordinated actions of three proteins: Dnm1p, a dynamin-related GTPase; Mdv1p, a WD domain protein; and Fis1p, a small integral outer membrane protein . Current data suggest that Dnm1p is localized to punctate structures that are targeted to the outer mitochondrial membrane by Fis1p where it mediates fission in an Mdv1p- and Fis1p-dependent manner5i}}*r, 百拇医药
In contrast to mitochondrial fission, the mechanism whereby the outer and inner mitochondrial membranes are coordinately fused is less clear. Until recently, the only known component involved in mitochondrial fusion was Fzo1p, a novel GTPase with homologues in Drosophila melanogaster and humans . In S. cerevisiae, mutations in, or deletion of, FZO1 cause mitochondria to fragment, a phenotype consistent with a block in fusion. Based on kinetic analysis, mitochondrial DNA (mtDNA) loss is thought to be a secondary consequence of mitochondrial fragmentation in fzo mutants . Interestingly, disruption of fission in fzo1 mutants suppresses mitochondrial fragmentation and restores mitochondrial tubules, but does not restore mitochondrial fusion during mating, indicating that FZO1 plays a direct role in this process
Recently, two genes, named UGO1 and UGO2, were identified in a genetic screen for mutations that caused DNM1-dependent loss of mitochondrial DNA and were shown to be required for mitochondrial fusion during mating . To date, the sequence of the UGO2 gene has not been reported. However, UGO1 encodes a 58-kD integral outer mitochondrial membrane protein with its NH2 terminus in the cytosol and its COOH terminus in the intermembrane space. In a manner identical to fzo1 mutants, ugo mutants have fragmented mitochondria and lose mtDNA during cell division. Disruption of fission in a ugo1 background restores mitochondrial tubules, but not mitochondrial fusion, consistent with a direct role in mitochondrial fusion . Interestingly, localization of Ugo1p's domains in both the cytosol and the intermembrane space suggests that it could interact with components both inside and outside of the organelle.'y?#&, http://www.100md.com
Mutations in MGM1, a dynamin-related GTPase, also were found to cause fragmentation and aggregation of mitochondria with secondary loss of mtDNA, raising the possibility that MGM1 might function in fusion . In addition, mitochondrial fragmentation and mtDNA loss in mgm1 mutants are suppressed when fission is abolished by deletion of DNM1 . However, in contrast to fzo1ts cells, deletion of DNM1 in mgm1ts cells restores mitochondrial fusion during mating. This observation suggests that MGM1 may not be directly involved in fusion
Structural Mgm1p homologues have been identified in higher eukaryotes, where they also have been shown to regulate mitochondrial morphology and function . Interestingly, the human homologue of Mgm1p, OPA1, was shown to be mutated in individuals with autosomal dominant optic atrophy, indicating the important role that mitochondrial structure plays in cellular function . The reported submitochondrial localization of Mgm1p homologues, however, has been conflicting. Data from both protease protection and immuno-EM analyses indicate that Mgm1p is localized to the intermembrane space, associated with the inner mitochondrial membrane. A previous study reported an outer membrane localization of Mgm1p , and the Schizosaccharomyces pombe homologue, Msp1p, was reported to be localized to the mitochondrial matrix, associated with the inner membrane . Recently, however, OPA1 was reported to reside in the mitochondrial intermembrane space, associated with the inner membrane, in agreement with findings on Mgm1p's localization by
In this report, we show that blocking DNM1-dependent fission in mgm1 cells does not restore mitochondrial fusion during mating. This observation is in contrast to our previous results where fusion was observed during mating in mgm1ts dnm1 cells . To address whether Mgm1p plays a direct role in fusion, we have performed cytological, biochemical, and genetic analyses. We show that Mgm1p is in a complex with two mitochondrial fusion components that reside in the outer membrane, Ugo1p and Fzo1p, and that its GTPase and assembly activities are required for mitochondrial fusion. Taken together, our data suggest a model where Mgm1p functions to remodel inner membranes and, through its association with outer membrane components, coordinates the behavior of the inner and outer membranes during fusion.2rt%:), http://www.100md.com
Results and discussion2rt%:), http://www.100md.com
MGM1 is required for mitochondrial fusion2rt%:), http://www.100md.com
Deletion of, or mutations in, MGM1 causes mitochondrial fragmentation and a subsequent loss of mitochondrial DNA in a similar fashion to mutations in FZO1 or UGO1, two genes required for mitochondrial fusion . We previously reported that mgm1 mutants also failed to fuse during mating, suggesting that MGM1 plays a role in fusion . We asked if this block in fusion was due to structural limitations of fragments, or whether MGM1 plays a direct role in fusion by deleting the dynamin-related GTPase DNM1 to disrupt fission in mgm1 mutants. We found that deletion of DNM1 in mgm1ts mutants blocked mitochondrial fragmentation and restored mitochondrial tubules, in an identical fashion to fzo1 and ugo1 mutants. Restoration of mitochondrial tubules in mgm1ts cells, as assessed by mitochondrial morphology and growth, was accompanied by restored mitochondrial fusion unpublished data). This is in contrast to fzo1-1 dnm1 mutants, where mitochondrial tubules are restored, but mitochondrial fusion is blocked
In the present study, we assayed for mitochondrial fusion in mgm1dnm1 cells during mating. As shown in , we observed that, as expected, mitochondrial fragmentation due to loss of MGM1 function was suppressed by blocking DNM1-dependent fission, and tubules were restored (E–H). However, in contrast to wild-type and mgm1tsdnm1 cells , mitochondrial fusion was blocked in mgm1dnm1 cells (, E–H, 8% unfused, n = 50; I–L, 98% unfused, n = 50), a phenotype identical to that observed for fzo1dnm1 cells (, N–P). One explanation for this observed difference between mgm1 and mgm1ts strains is that the mgm1ts alleles tested are hypomorphs and, when shifted to the nonpermissive temperature, retain enough function to support mitochondrial fusion. In this case, Mgm1p may be essential for mitochondrial fusion, and our observations indicate that the requirement for Mgm1p function in fusion is diminished in the context of mitochondrial tubules, as opposed to mitochondrial fragments. Alternatively, it is possible that mitochondrial fusion is abolished in mgm1dnm1 cells as a secondary, indirect consequence of loss of MGM1 function.
fig.ommtted:0z\/7c, http://www.100md.com
MGM1 is required for mitochondrial fusion during mating. Cells of the opposite mating type expressing either mito–GFP or mito–RFP were grown to log phase at 25°C, mated at 37°C, and imaged as previously described . Mitochondrial fusion was assessed by examining merged mito–GFP and mito–RFP images of large-budded homozygous zygotes formed from wild type (A–D), mgm1–5dnm1 (E–H), mgm1dnm1 (I–L), and fzo1dnm1 (M–P). Bars, 2 µm.:0z\/7c, http://www.100md.com
fig.ommtted:0z\/7c, http://www.100md.com
Mgm1p, Ugo1p, and Fzo1p interact. (A) Immunoprecipitations were performed using anti-HA on cross-linked mitochondrial fractions isolated from MGM1:3XHA (lanes 1 and 2), UGO1:3XHA (lanes 3 and 4), wild-type (lanes 5 and 6), and mgm1 UGO1:3XHA (lanes 7 and 8) strains. The total and immunoprecipitated pellet fractions were probed with antibodies as described in the Materials and methods. The amount loaded from the total fraction is equivalent to 2.5% of the bound fraction. (B) Mitochondrial extracts from UGO1:3XHA (lanes 1 and 2), mgm1 UGO1:3XHA (lanes 3 and 4), and fzo1 UGO1:3XHA (lanes 5 and 6) were immunoprecipitated using anti-Mgm1 antibodies. The total and pellet fractions were analyzed by Western blotting with anti-HA. Ugo1:3XHAp is designated Ugo1HA in the figure.
Mgm1p, Ugo1p, and Fzo1p interact;*p46, 百拇医药
To examine these two possibilities, we tested the relationship of Mgm1p to two known fusion components, Ugo1p and Fzo1p, by performing immunoprecipitation reactions. Immunoprecipitations were performed on mitochondrial-enriched fractions isolated from wild-type cells or cells expressing either a previously characterized and functional internally HA-tagged version of Mgm1p (Mgm1:3XHAp) or a functional COOH-terminal HA epitope–tagged allele of Ugo1p (Ugo1:3XHAp) using both mouse monoclonal anti-HA antibodies and polyclonal anti-Mgm1 antibodies . We were unable to detect interactions among Mgm1p, Fzo1p, and Ugo1p in native cell extracts, suggesting that they might be labile in vitro. To overcome this instability, before immunoprecipitation, proteins were cross-linked in mitochondrial fractions with the bifunctional, reversible cross-linker dithiobis-(succinimidyl propionate) (DSP) and extracted under denaturing conditions. After immunoprecipitation, cross-links were reversed with reducing agents and precipitates were analyzed by SDS-PAGE and Western blotting.
We first examined whether Mgm1p and Ugo1p interact with Fzo1p by performing immunoprecipitations using anti-HA antibodies from cross-linked Mgm1:3XHA-tagged and Ugo1:3XHA-tagged mitochondrial extracts. Western blot analysis with anti-Fzo1p antibodies of fractions from mitochondrial extracts immunoprecipitated with anti-HA antibodies demonstrated that a fraction of Fzo1p was reproducibly coimmunoprecipitated with either Mgm1p or Ugo1p ( A, lanes 1–4). As expected, the majority of Ugo1:3xHA and Mgm1:3XHA were specifically recovered in immunoprecipitate fractions from cells that expressed these proteins (unpublished data). In contrast, neither the outer mitochondrial membrane fission component, Fis1p, nor the inner membrane protein import component, Tim44p, was observed in the immunoprecipitate fraction, indicating that the interaction of Ugo1p and Mgm1p with Fzo1p is specific ( A, lanes 1–4). In addition, Tim23p, an inner membrane import component that contains an intermembrane space domain, also was not recovered in the immunoprecipitate (unpublished data). To further address specificity, immunoprecipitations were performed from enriched, DSP–cross-linked mitochondrial fractions isolated from wild-type cells, not expressing either Ugo1:3XHA or Mgm1:3XHA. Under these conditions, Fzo1p was not recovered in the immunoprecipitate fraction, indicating that the coimmunoprecipitation of Fzo1p with the anti-HA antibody is dependent on the HA-tagged versions of Ugo1p and Mgm1p ( A, lanes 5 and 6).
To further examine the nature of Ugo1p's interactions with Fzo1p, immunoprecipitation experiments were performed using a DSP–cross-linked mitochondrial fraction isolated from mgm1 Ugo1HA cells. Interestingly, Western blot analysis of fractions from anti-HA immunoprecipitations in mgm1 Ugo1:3XHA mitochondria revealed that although Fzo1p was present at lower levels, it coimmunoprecipitated with anti-HA antibodies, indicating that an Fzo1p–Ugo1p interaction occurs independently of Mgm1p ( A, lanes 7 and 8). Interestingly, the level of Fzo1p in total mgm1 Ugo1:3XHA yeast extracts prepared under denaturing conditions was similar to that observed in wild-type Ugo1:3XHA extracts (unpublished data). Thus, Fzo1p's instability in the mitochondrial fraction from mgm1 Ugo1:3XHA cells probably results from proteolysis in vitro. These observations suggest that in the absence of Mgm1p, Fzo1p may be present in mitochondrial membranes in an altered conformation, consistent with our observation of an Fzo1p–Mgm1p interaction.
Our observations indicate that both Mgm1p and Ugo1p are present in a complex(es) with Fzo1p. To determine whether Mgm1p also is present in a complex containing Ugo1p, we performed immunoprecipitations using anti-Mgm1p antibodies from cross-linked Ugo1:3XHA-tagged mitochondria. Significantly, we observed that a fraction of Ugo1p was specifically and reproducibly coimmunoprecipitated with Mgm1p ( B, lanes 1–4). Interestingly, Ugo1p coimmunoprecipitated with Mgm1p in the absence of Fzo1p, indicating that the interaction observed between Mgm1p and Ugo1p occurs independently of Fzo1p ( B, lanes 5 and 6). Taken together, these biochemical data demonstrate that Mgm1p forms a complex(es) with two known fusion components, Ugo1p and Fzo1p, and support a direct role for Mgm1p in mitochondrial fusion.e;d{1, 百拇医药
Mgm1p behaves as a dynamin-related GTPasee;d{1, 百拇医药
In addition to a GTPase domain, dynamin-related GTPases share a middle domain and an assembly or GTPase effector domain (GED) . These additional domains function together with the GTPase domain to promote the self-assembly of dynamin-related GTPases into ring and spiral-like structures, resulting in a stimulation of GTPase activity Both the self-assembly and GTPase activities of dynamin-related GTPases have been shown to be important for their ability to remodel biological membranes . To further characterize Mgm1p's role in fusion, we examined whether mutations predicted to affect the GTPase and self-assembly activities of Mgm1p would affect its ability to promote mitochondrial fusion.
We created mutants predicted to be defective in the GTPase cycle, based on the analysis of dynamin and other GTPase superfamily members, by mutating specific conserved residues in the G1 and G2 nucleotide binding regions of Mgm1p. Conserved residues in the G1 region, K223 and S224, and in the G2 region, T244, were mutated to alanine in Mgm1p. We first examined the expression of these mutant forms of Mgm1p in mgm1 cells by Western blotting. Interestingly, only Mgm1S224A and Mgm1T244A were detected in cells, suggesting that the nucleotide binding state of Mgm1p affects its stability in vivo (; unpublished data).7t, 百拇医药
fig.ommtted7t, 百拇医药
Determination of the steady-state levels of mutant Mgm1 proteins. JNY845 was transformed with pRS425 vectors containing mgm1 mutants, and strains were grown overnight to log phase. Whole cell extracts were made and analyzed by SDS-PAGE followed by Western blotting as described in the Materials and methods. Western analysis of the cytosolic protein 3-phosphoglycerokinase (PGK) was used as a loading control.
Mutations of S224 in the G1 region of Mgm1p are predicted to alter nucleotide binding, and mutations in T244 in the G2 region of Mgm1p are predicted to stabilize the protein in the GTP-bound form . Recently, however, a careful analysis of the effects of similar mutations on dynamin's ability to bind and hydrolyze GTP revealed that they did not produce the predicted effects and instead destabilized the binding of both GDP and GTP to mutant proteins . Nevertheless, we determined the ability of these Mgm1 mutant proteins to complement both the mitochondrial morphology and fusion defects in mgm1 cells.)!, 百拇医药
Both the S224A and T244A Mgm1p mutants were unable to support wild-type levels of Mgm1p function . Specifically, these mutants were unable to fully complement the mitochondrial morphology defect of mgm1 cells and also failed to completely restore the ability of mitochondria to fuse during mating in mgm1dnm1 cells, where mitochondrial tubules were restored. Interestingly, when Mgm1S224A and Mgm1T224A were overexpressed in wild-type cells, they interfered to varying degrees and in a dose-dependent manner with wild-type MGM1 function, as assessed by mitochondrial morphology, similar to observations of dynamin and Dnm1p mutants . These observations are consistent with a previous study reporting that Mgm1S224Np failed to complement the mitochondrial morphology defect in mgm1 cells and displayed a dominant negative phenotype when overexpressed in wild-type cells . We conclude that Mgm1p's GTPase cycle is essential for its ability to function in mitochondrial fusion.
fig.ommttedm, 百拇医药
Mutations in Mgm1p's GTPase and GTPase effector domains affect mitochondrial morphology and fusionm, 百拇医药
fig.ommttedm, 百拇医药
Mutations in Mgm1p's GTPase and GTPase effector domains cause dose-dependent dominant negative effects on mitochondrial morphologym, 百拇医药
Intermolecular interactions are required for dynamin and dynamin-related GTPases to function (for review see ). Our observation that overexpression of Mgm1p GTPase mutants induced mitochondrial fragmentation in wild-type cells is consistent with the possibility that mutant Mgm1p coassembles and interferes with the function of wild-type Mgm1p and suggests that Mgm1p self-assembly is required for its function in fusion. To further test this, we examined the role of Mgm1p's putative GED in mitochondrial fusion. Lysine and arginine residues in dynamin's GED have been shown previously to play a role in assembly and assembly-stimulated GTPase activity To test the role of these basic residues, we mutated all of the arginine and lysine residues in Mgm1p's predicted GED to alanine and assessed the function of these mutant proteins by examining mitochondrial morphology and fusion in cells. Interestingly, two mutations in MGM1's predicted GED domain, R824A and K854A, failed to completely restore mitochondrial morphology in mgm1 cells and mitochondrial fusion during mating in mgm1dnm1 cells . Western blot analysis of cells showed that these mutant proteins were expressed at levels comparable to wild-type Mgm1p, indicating that loss of function was not the result of protein instability. In the case of Mgm1S224A and Mgm1K854A mutants, the defect observed in mitochondrial fusion in mgm1nm1 cells was less severe than that observed for mitochondrial morphology in mgm1 cells. This discrepancy could be explained if the requirement for Mgm1p function in fusion is diminished in the context of mitochondrial tubules, as opposed to mitochondrial fragments, which also may explain our previous observations for mgm1ts cells . Similar to Mgm1p GTPase mutants, when Mgm1R824A and Mgm1K854A were overexpressed in wild-type cells, they interfered to varying degrees and in a dose-dependent manner with wild-type MGM1 function, as assessed by mitochondrial morphology . These observations indicate that Mgm1p's GED is important for its function and suggest that Mgm1p self-assembly occurs and is important for the ability of Mgm1p to facilitate mitochondrial fusion.
To further test whether Mgm1p self-assembles in vivo, we analyzed diploids from crosses of several mgm1ts mutants, previously isolated in a forward genetic screen for mutants unable to maintain mtDNA at elevated temperatures . We reasoned that if Mgm1p self-interacts, two different mutations in MGM1 may be able to compensate for one another within an assembled Mgm1p complex and restore mitochondrial fusion activity, resulting in maintenance of mtDNA and growth on a nonfermentable carbon source at the nonpermissive temperature. Interestingly, the entire collection of mgm1ts mutants isolated in the screen contained mutations only in either the GTPase domain or the GED, underscoring the importance of these domains in MGM1 function ( A; unpublished data). A combination of a subset of these mgm1ts alleles in diploids grew at the nonpermissive temperature on media containing glycerol, indicating that they displayed intragenic complementation . In total, data from our genetic analysis of mgm1 mutants support a model where Mgm1p functions in fusion as a self-assembling GTPase.
fig.ommttedlwwu!2, http://www.100md.com
Intragenic complementation is observed between mgm1 temperature-sensitive mutants. (A) Schematic of MGM1 domain structure designating the position of the temperature-sensitive mutations analyzed for intragenic complementation is shown. (B) Analysis of intragenic complementation of mgm1ts alleles. Growth on glycerol is indicated by +.lwwu!2, http://www.100md.com
Mgm1p is an intermembrane space proteinlwwu!2, http://www.100md.com
We previously reported that Mgm1p is an intermembrane space protein based on data from protease protection experiments of intact and hypo-osmotically shocked mitochondria. Protease protection experiments, however, are technically difficult in that isolated mitochondria must be intact and hypo-osmotic conditions for selectively disrupting the outer mitochondrial membrane are variable. Because of these difficulties, and the reported differing submitochondrial localizations of Mgm1p and its S. pombe orthologue, Msp1p, we reexamined Mgm1p's submitochondrial localization using a novel method involving the tobacco etch virus (TEV) protease.
Tobacco etch virus has a 27-kD protease subunit that specifically cleaves proteins containing the consensus sequence EXXYXQØS, which is absent from all predicted ORFs from the yeast genome . For this reason, it has been used successfully to examine the in vivo topology of proteins. We obtained plasmids harboring genes encoding active mitochondrial matrix (matrix-TEV)– and intermembrane space (IMS-TEV)–targeted versions of TEV, constructed using the well-defined targeting sequences of ATP9 and CYB2, respectively (Thatcher, J., and J. Shaw, personal communication).88rvyp?, http://www.100md.com
To determine the localization of Mgm1p in vivo, MGM1:3XHA, contained on a CEN/ARS plasmid, was engineered with a sequence encoding a TEV consensus cleavage site directly preceding the coding sequence of the 3XHA tag (MGM1:tev:3XHA). Interestingly, this version of MGM1 maintained function, as assessed by its ability to support the growth of {Delta} mgm1 cells on media containing a nonfermentable carbon source (unpublished data). Given the internal position of the TEV cleavage site and the 3XHA tag, cleavage of Mgm1:tev:3XHAp by TEV is predicted to produce a product of ~
75 kD, specifically detected by Western analysis using anti-HA antibodies.nq/ns(, 百拇医药
Western blot analysis of mitochondrial fractions isolated from wild-type cells expressing Mgm1:tev:3XHAp alone with anti-HA antibodies revealed two predominant forms of Mgm1:tev:3XHAp, as seen previously in cells expressing both Mgm1:3XHAp and native, untagged Mgm1p (, lane 1). When coexpressed with matrix-TEV, the two Mgm1:tev:3XHAp products remained unchanged (, lane 2). In contrast, an additional, faster-migrating species, estimated at 75 kD, was detected with anti-HA antibodies in cells coexpressing Mgm1:tev:3XHAp and IMS-TEV (, lane 3, asterisk). The apparent molecular mass of this species is in agreement with the size of a predicted TEV-dependent cleavage product of Mgm1:tev:3XHAp and indicates that Mgm1p was accessible only to the IMS-targeted version of TEV. This observation confirms our previously published results that Mgm1p is localized to the intermembrane space and is in agreement with the recently published localization of the human Mgm1p orthologue, OPA1
fig.ommtted44!-0, 百拇医药
Mgm1p is in the IMS compartment in vivo. Mitochondria were isolated from strains expressing Mgm1:tev:3XHAp alone (lane 1), Mgm1:tev:3XHAp and ATP9-TEVp (lane 2), and Mgm1:tev:3XHAp and CYB2-TEVp (lane 3) and analyzed by SDS-PAGE followed by Western blotting with anti-HA and anti-porin antibodies, as a loading control. Asterisk indicates a TEV-specific Mgm1 cleavage product.44!-0, 百拇医药
Our previous immuno-EM observations of Mgm1p indicate that it is associated with the mitochondrial inner membrane . Since our report, additional observations have been made that substantiate this conclusion. In a study that revealed a role for ATP synthase in the formation of mitochondrial inner membrane cristae structures in yeast, the localization of the outer membrane protein porin and the inner membrane–associated ß subunit of ATP synthase were determined by immuno-EM In the case of the ß subunit of ATP synthase, gold particles were observed in the interior of mitochondria, in most cases clearly associated with cristae, similar to the pattern we observed for Mgm1p. In contrast, in the case of porin, the majority of gold particles were associated with the periphery of mitochondria, consistent with an outer membrane localization . In addition, immuno-EM localization of OPA1 indicates that it is localized within mitochondria, associated with cristae membranes, in a pattern similar to that observed for Mgm1p . Thus, taken together, these observations substantiate our previous report of Mgm1p topology, where it is tightly associated with the inner membrane, with its GTPase domain localized to the intermembrane space compartment
A model for Mgm1p function during mitochondrial fusion]k\l, 百拇医药
The data presented in this paper support a model where the intermembrane space protein Mgm1p functions in fusion as a self-assembling GTPase and plays a role in coordinating the inner and outer membranes during the fusion process. As a self-assembling GTPase, Mgm1p may directly promote the fusion of the inner membrane by helping to form a transient tubule or protrusion of this membrane, similar to the role proposed for the dynamin-related GTPase phragmoplastin in cell plate formation in plants . This Mgm1p-dependent inner membrane remodeling event may be regulated by fusion-promoting events in the outer membrane via Mgm1p's interaction with Ugo1p and Fzo1p. In addition, Mgm1p's interactions with Ugo1p and Fzo1p may serve to physically coordinate the behavior of both membranes and promote the formation of a double membrane structure with a higher radius of curvature, thereby producing a fusion-competent microenvironment. Alternatively, Mgm1p might function as a classical GTPase that recruits Fzo1p and Ugo1p, which in turn promote fusion, similar to the role proposed for dynamin during endocytosis. Recently it was reported that deletion of several novel ORFs encoding predicted inner mitochondrial membrane proteins caused mitochondrial fragmentation and mtDNA loss in cells, similarly to fzo1, ugo, and mgm1 mutants . Given their predicted localization and mutant phenotypes, it is attractive to speculate that these components may play a role in mitochondrial fusion by modulating Mgm1p function. Elucidating the exact role of these components in mitochondrial morphology will help illuminate the complex process of coordinately fusing four mitochondrial membranes.
Materials and methodss.!|'\, http://www.100md.com
Plasmid and strain construction and analysiss.!|'\, http://www.100md.com
Strains used in this study are summarized in . Temperature-sensitive MGM1 alleles were isolated in a previous screen and mutations were identified by amplifying the MGM1 locus in mutant cells by PCR using Vent polymerase and sequencing the products directly (Davis Sequencing, University of California, Davis). To mutagenize MGM1, XbaI sites flanking the MGM1 locus with its native promoter were engineered by PCR. The entire locus was subcloned into pRS425 or pRS315 . Point mutations in MGM1 were created using a QuikChange mutagenesis kit. Mutations were confirmed by sequence analysis of the entire MGM1 insert (DBS sequencing facility, Section of Molecular and Cellular Biology, University of California, Davis). A yeast strain harboring a COOH-terminal 3XHA–tagged version of Ugo1p was created by homologous recombination between the UGO1 locus in JSY1826 cells and a PCR product as previously described . This strain, JNY894, was confirmed by PCR of the UGO1 locus and Western blotting using anti-HA antibodies (Covance Research). Strains JNY898 and JNY903 were obtained by crossing, sporulation, and tetrad analysis. To construct a TEV cleavage site within Mgm1p, XbaI sites flanking MGM1:3XHA with its native promoter were engineered by PCR from genomic JSY2519 DNA. The XhoI to EcoRI and NotI to SalI restriction sites were destroyed in pRS313 to create pEDI14. MGM1:3XHA was nondirectionally cloned into pEDI14 using the engineered XbaI sites. A TEV protease site was created by annealing complementary oligonucleotide primers to the following sequence: TCG ACG AAA ACT TGT ATT TTC AAG GTG and TCG ACA CCT TGA AAA TAC AAG TTT TCG. This TEV site was inserted into a unique XhoI site preceding the sequence encoding 3XHA in MGM1:3XHA, destroying the XhoI site and creating MGM1p:tev:3XHA. Whole cell extracts were prepared as previously described . Mitochondrial morphology and mitochondrial fusion during mating were analyzed as previously described
fig.ommtted/:1tn, 百拇医药
Strains used in this study/:1tn, 百拇医药
Immunoprecipitation of cross-linked mitochondrial proteins/:1tn, 百拇医药
To enrich for mitochondrial proteins, mitochondria were isolated by differential centrifugation as previously described , except that the mitochondrial fraction was pelleted only once. The mitochondrial-enriched membrane fraction resulting from 100 OD600 of spheroplasts was resuspended in 500 µl mitochondrial isolation buffer (20 mM Hepes, pH 7.5, 600 mM sorbitol, and 1x protease inhibitors). To cross-link associated proteins, DSP was added to a final concentration of 1 mM and incubated at 0°C for 2 h. Cross-linking was stopped by the addition of 100 mM glycine, pH 8.0, followed by precipitation of proteins using trichloroactetic acid (final concentration 10% wt/vol). Mitochondrial proteins were denatured and solubilized by suspension in 100 µl MURB (100 mM MES, pH 7, 1% SDS, 3 M urea) and incubated at 65°C for 5 min, followed by the addition of 750 µl TWIP (50 mM Tris-Cl, pH 7.5, 150 mM NaCl, 0.5% Tween 20, 0.1% EDTA). The supernatant fraction was incubated overnight at 4°C with 75 µl protein A agarose beads with gentle rocking. Protein A agarose beads were washed three times with 1 ml TWIP. Bead pellets were resuspended in MURB with 5% ß-mercaptoethanol and incubated at 65°C for 10 min to release proteins into the sample buffer and reduce cross-links. Protein in total and protein A agarose–bound fractions were analyzed by SDS-PAGE followed by Western blot analysis.
In vivo localization of Mgm1p(6g3%, 百拇医药
GAL1-regulated matrix and IMS-targeted versions of TEV protease were were provided by J. Thatcher and J. Shaw (University of Utah, Salt Lake City, UT). Plasmids were cotransformed into strains with MGM1:tev:3XHAp and cells were grown to log phase in selective media containing raffinose. TEV expression was induced by subculturing cells in media containing galactose, and proteolysis of Mgm1:tev:3XHAp by TEV protease was determined by the analysis of mitochondria-enriched fractions after growth in galactose-containing media for 30 min using SDS-PAGE and Western blotting.(6g3%, 百拇医药
SDS-Page and Western blot analysis(6g3%, 百拇医药
All protein samples were analyzed by gel electrophoresis using 12.5% Anderson polyacrylamide gels as previously described . Proteins were transferred to a nitrocellulose membrane and analyzed using primary antibodies to Tim44p (1:1,000; Debukmar Pain), anti-Fis1p (1:2,000), Mgm1p (1:200), HA (1:2,500; Covance), 3-phosphoglycerokinase (PGK) (1:1,000; Molecular Probes, Inc.), GFP (1:10,000; Covance), and Fzo1p (1:1,000; provided by J. Shaw) in PBS-T plus 5% dry milk. Rabbit polyclonal anti-Mgm1p antibodies were raised against bacterial-expressed Mgm1p region (amino acids 490–902) from pET28aMGM1490–902 (Covance). Proteins were visualized by incubation with the appropriate secondary antibody conjugated to horseradish peroxidase (1:5,000) in PBS-T plus 5% dry milk, followed by ECL
Acknowledgments$mu#, 百拇医药
We are grateful to John Thatcher and Janet Shaw for providing TEV reagents prior to publication. We are also grateful to members of the Nunnari lab for their critical input into this project.$mu#, 百拇医药
This work was supported by National Science Foundation REU grant to J. Nunnari.$mu#, 百拇医药
Submitted: 3 September 2002$mu#, 百拇医药
Revised: 19 December 2002$mu#, 百拇医药
Accepted: 20 December 2002$mu#, 百拇医药
References$mu#, 百拇医药
Alexander, C., M. Votruba, U.E.A. Pesch, D.L. Thiselton, S. Mayer, A. Moore, M. Rodriguez, U. Kellner, B. Leo-Kottler, G. Auburger, et al. 2000. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nat. Genet. 26:211–215.$mu#, 百拇医药
Bleazard, W., J.M. McCaffery, E.J. King, S. Bale, A. Mozdy, Q. Tieu, J. Nunnari, and J.M. Shaw. 1999. The dynamin-related GTPase Dnm1 regulates mitochondrial fission in yeast. Nat. Cell Biol. 1:298–304.
Bourne, H.R., D.A. Sanders, and F. McCormick. 1991. The GTPase superfamily: conserved structure and molecular mechanism. Nature. 349:117–127.)y@s, 百拇医药
Cerveny, K.L., J.M. McCaffery, and R.E. Jensen. 2001. Division of mitochondria requires a novel DNM1-interacting protein, Net2p. Mol. Biol. Cell. 12:309–321.)y@s, 百拇医药
Chernomordik, L.V., and J. Zimmerberg. 1995. Bending membranes to the task: structural intermediates in bilayer fusion. Curr. Opin. Struct. Biol. 5:541–547.)y@s, 百拇医药
Christianson, T.W., R.S. Sikorski, M. Dante, J.H. Shero, and P. Hieter. 1992. Multifunctional yeast high-copy-number vectors. Gene. 110:119–122.)y@s, 百拇医药
Damke, H., T. Baba, D.E. Warnock, and S.L. Schmid. 1994. Induction of mutant dynamin specifically blocks endocytic coated vesicle formation. J. Cell Biol. 127:915–934.)y@s, 百拇医药
Damke, H., D.D. Binns, H. Ueda, S.L. Schmid, and T. Baba. 2001. Dynamin GTPase domain mutants block endocytic vesicle formation at morphologically distinct stages. Mol. Biol. Cell. 12:2578–2589.)y@s, 百拇医药
Delettre, C., G. Lenaers, J.-M. Griffoin, N. Gigarel, C. Lorenzo, P. Belenguer, L. Pelloquin, J. Grosgeorge, C. Turc-Carel, E. Perret, et al. 2000. Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy. Nat. Genet. 26:207–210.
Dimmer, K.S., S. Fritz, F. Fuchs, M. Messerschmitt, N. Weinbach, W. Neupert, and B. Westermann. 2002. Genetic basis of mitochondrial function and morphology in Saccharomyces cerevisiae. Mol. Biol. Cell. 13:847–853.2, 百拇医药
Faber, K.N., A.M. Kram, M. Ehrmann, and M. Veenhuis. 2001. A novel method to determine the topology of peroxisomal membrane proteins in vivo using the tobacco etch virus protease. J. Biol. Chem. 276:36501–36507.2, 百拇医药
Fekkes, P., K.A. Shepard, and M.P. Yaffe. 2000. Gag3p, an outer membrane protein required for fission of mitochondrial tubules. J. Cell Biol. 151:333–340.2, 百拇医药
Hales, K.G., and M.T. Fuller. 1997. Developmentally regulated mitochondrial fusion mediated by a conserved, novel, predicted GTPase. Cell. 90:121–129.2, 百拇医药
Hermann, G.J., J.W. Thatcher, J.P. Mills, K.G. Hales, M.T. Fuller, J. Nunnari, and J.M. Shaw. 1998. Mitochondrial fusion in yeast requires the transmembrane GTPase Fzo1p. J. Cell Biol. 143:359–374.2, 百拇医药
Hinshaw, J.E. 2000. Dynamin and its role in membrane fission. Annu. Rev. Cell Dev. Biol. 16:483–519.
Hinshaw, J.E., and S.L. Schmid. 1995. Dynamin self-assembles into rings suggesting a mechanism for coated vesicle budding. Nature. 374:190–192.^v+[$#o, 百拇医药
Longtine, M., A. McKenzie, D. Demarini, N. Shah, A. Wach, A. Brachat, P. Philippsen, and J. Pringle. 1998. Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae. Yeast. 14:953–961.^v+[$#o, 百拇医药
Meeusen, S., Q. Tieu, E. Wong, E. Weiss, D. Schieltz, J.R. Yates, and J. Nunnari. 1999. Mgm101p is a novel component of the mitochondrial nucleoid that binds DNA and is required for the repair of oxidatively damaged mitochondrial DNA. J. Cell Biol. 145:291–304.^v+[$#o, 百拇医药
Misaka, T., T. Miyashita, and Y. Kubo. 2002. Primary structure of a dynamin-related mouse mitochondrial GTPase and its distribution in brain, subcellular localization, and effect on mitochondrial morphology. J. Biol. Chem. 277:15834–15842.^v+[$#o, 百拇医药
Mozdy, A.D., J.M. McCaffery, and J.M. Shaw. 2000. Dnm1p GTPase-mediated mitochondrial fission is a multi-step process requiring the novel integral membrane component Fis1p. J. Cell Biol. 151:367–380.
Muhlberg, A.B., D.E. Warnock, and S.L. Schmid. 1997. Domain structure and intramolecular regulation of dynamin GTPase. EMBO J. 16:6676–6683.k, 百拇医药
Nunnari, J., W. Marshall, A. Straight, A. Murray, J.W. Sedat, and P. Walter. 1997. Mitochondrial transmission during mating in S. cerevisiae is determined by mitochondrial fusion and fission and the intramitochondrial segregation of mtDNA. Mol. Biol. Cell. 8:1233–1242.k, 百拇医药
Okamoto, P.M., B. Tripet, J. Litowski, R.S. Hodges, and R.B. Vallee. 1999. Multiple distinct coiled-coils are involved in dynamin self-assembly. J. Biol. Chem. 274:10277–10286.k, 百拇医药
Olichon, A., L.J. Emorine, E. Descoins, L. Pelloquin, L. Brichese, N. Gas, E. Guillou, C. Delettre, A. Valette, C.P. Hamel, et al. 2002. The human dynamin-related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter-membrane space. FEBS Lett. 523:171–176.k, 百拇医药
Otsuga, D., B.R. Keegan, E. Brisch, J.W. Thantcher, G.J. Hermann, W. Bleazard, and J. Shaw. 1998. The dynamin GTPase, Dnm1p, controls mitochondrial morphology in yeast. J. Cell Biol. 143:333–349.
Paumard, P., J. Vaillier, B. Coulary, J. Schaeffer, V. Soubannier, D.M. Mueller, D. Brethes, J.-P. di Rago, and J. Velours. 2002. The ATP synthase is involved in generating mitochondrial cristae morphology. EMBO J. 21:221–230.j$?$!u, 百拇医药
Pelloquin, L., P. Belenguer, Y. Menon, N. Gas, and B. Ducommun. 1999. Fission yeast msp1 is a mitochondrial dynamin-related protein. J. Cell Sci. 112:4151–4161.j$?$!u, 百拇医药
Rapaport, D., M. Brunner, W. Neupert, and B. Westermann. 1998. Fzo1p is a mitochondrial outer membrane protein essential for the biogenesis of functional mitochondria in Saccharomyces cerevisiae. J. Biol. Chem. 273:20150–20155.j$?$!u, 百拇医药
Samuels, A.L., T.H. Giddings, and L.A. Staehelin. 1995. Cytokinesis in tobacco BY-2 and root tip cells: a new model of cell plate formation in higher plants. J. Cell Biol. 130:1345–1357.j$?$!u, 百拇医药
Santel, A., and M.T. Fuller. 2001. Control of mitochondrial morphology by a human mitofusin. J. Cell Sci. 114:867–874.j$?$!u, 百拇医药
Sesaki, H., and R.E. Jensen. 1999. Division versus fusion: Dnm1p and Fzo1p antagonistically regulate mitochondrial shape. J. Cell Biol. 147:699–706.
Sesaki, H., and R.E. Jensen. 2001. UGO1 encodes an outer membrane protein required for mitochondrial fusion. J. Cell Biol. 152:1123–1134..6, http://www.100md.com
Sever, S., A.B. Muhlberg, and S.L. Schmid. 1999. Impairment of dynamin's GAP domain stimulates receptor-mediated endocytosis. Nature. 398:481–486..6, http://www.100md.com
Sever, S., H. Damke, and S.L. Schmid. 2000. Dynamin:GTP controls the formation of constricted coated pits, the rate limiting step in clathrin-mediated endocytosis. J. Cell Biol. 150:1137–1147..6, http://www.100md.com
Shaw, J.M., and J. Nunnari. 2002. Mitochondrial dynamics and division in budding yeast. Trends Cell Biol. 12:178–184..6, http://www.100md.com
Shepard, K., and M. Yaffe. 1999. The yeast dynamin-like protein, Mgm1p, functions on the mitochondrial outer membrane to mediate mitochondrial inheritance. J. Cell Biol. 144:711–719..6, http://www.100md.com
Smirnova, E., D.-L. Shurland, E.D. Newman-Smith, B. Pishvaee, and A.M. van der Bliek. 1999. A model for dynamin self-assembly based on binding between three different protein domains. J. Biol. Chem. 274:14942–14947.
Smith, T.A., and B.D. Kohorn. 1991. Direct selection for sequences encoding proteases of known specificity. Proc. Natl. Acad. Sci. USA. 88:5159–5162.&*8, http://www.100md.com
Tieu, Q., and J. Nunnari. 2000. Mdv1p is a WD repeat protein that interacts with the dynamin-related GTPase, Dnm1p, to trigger mitochondrial division. J. Cell Biol. 151:353–365.&*8, http://www.100md.com
Tieu, Q., V. Okreglak, K. Naylor, and J. Nunnari. 2002. The WD repeat protein, Mdv1p, functions as a molecular adaptor by interacting with Dnm1p and Fis1p during mitochondrial fission. J. Cell Biol. 158:445–452.&*8, http://www.100md.com
van der Bliek, A.M. 1999. Functional diversity in the dynamin family. Trends Cell Biol. 9:96–102.&*8, http://www.100md.com
Verma, D.P., and X. Gu. 1996. Vesicle dynamics during cell-plate formation in plants. Trends Plant Sci. 1:145–149.&*8, http://www.100md.com
Wong, E.D., J.A. Wagner, S.W. Gorsich, J.M. McCaffery, J.M. Shaw, and J. Nunnari. 2000. The dynamin-related GTPase, Mgm1p, is an intermembrane space protein required for maintenance of fusion competent mitochondria. J. Cell Biol. 151:341–352.&*8, http://www.100md.com
Zhang, P., and J.E. Hinshaw. 2001. Three-dimensional reconstruction of dynamin in the constricted state. Nat. Cell Biol. 3:922–926.(Edith D. Wong Jennifer A. Wagner Sidney V. Scott Voytek Okreglak Timothy J. Holewinske Ann Cassidy-S)