核基质MINT N端片段(365~1084aa)相互作用蛋白的筛选及鉴定
酵母双杂交,,核蛋白MINT;,MSX2;,RBPJκ;,Notch信号途径;,酵母双杂交,核基质MINTN端片段(365~1084aa)相互作用蛋白的筛选及鉴定,0引言,1材料和方法,2结果
Screening and identification of nuclear matrix protein MINT Nterminal fragment (365-1084aa) interacting proteinsQIN Hong, SUN Qiang, ZHOU Peng, LI JunFeng, HAN Hua, LUO XiaoXing
1Departerment of Medical Genetics and Development Biology, 3Departerment of Pharmacology, School of Basic Medicine, Fourth Military Medical Univercity, Xi’an 710033, China, 2For Stem Cell Center, Tangdu Hospital, Fourth Military Medical Univercity, Xi’an 710038, China
【Abstract】 AIM: To identify the function and mechanism of nuclear matrix protein MINT (Msx2interacting nuclear target protein). METHODS: Yeast twohybrid assay was used to screen proteins that interact with a fragment of MINTF2 (365-1084aa). From 1.0×108 yeast clones transformed with the bait plasmid and a cDNA library of 9 dpc mouse embryo,128 were positive for nutritional screening and βgalactosidase assay. Restriction digestion showed 4 independent positive clones and they were analyzed by DNA sequencing, and revealed that they represent correctly fused cDNA fragments. RESULTS: Screened 4 proteins that interacting with MINTF2, which are 67 ku laminin receptor, two of 16 S ribosomal RNA, ArginyltRNA synthetase. CONCLUSION: Succeed screening of interacting with MINTF2 proteins, and made the basement for further study of the function and mechanism of MINT. ......
您现在查看是摘要页,全文长 10123 字符。