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作 者:郭芬[1,2] 李月琴[1] 李实骞[1] 罗志文[1] 张欣[1] 周天鸿[1]
机构地区:[1]暨南大学生命科学技术学院生物工程学系,广东广州510632 [2]广东药学院生命科学与生物制药学院,广东广州510006
出 处:《暨南大学学报(自然科学与医学版)》2010年第3期307-311,共5页Journal of Jinan University(Natural Science & Medicine Edition)
基 金:广东省自然科学基金项目(8151063201000013);高等学校博士学科点专项科研基金项目(20060559006)
摘 要:研究含外显子8的prosaposin蛋白亚型(PsapE8)与同源异型框蛋白Rhox5蛋白间的相互作用.重叠延伸PCR法扩增PsapE8的cDNA序列,将其按照通读框方式分别克隆至pGBKT7和pGADT7酵母双杂交载体中构建pGBKT7-PsapE8和pGADT7-PsapE8重组质粒.酵母双杂交实验检测PsapE8与Rhox5蛋白在酵母体内的结合;体外转录翻译S35标记的PsapE8蛋白,GSTpull-down实验检测PsapE8与Rhox5蛋白在体外的结合情况.成功地构建了pGBKT7-PsapE8和pGADT7-PsapE8重组质粒,酵母双杂交实验表明PsapE8蛋白在酵母体内可以结合Rhox5蛋白;GST pull-down实验再次验证了两者在体外的结合;表明含有外显子8的prosaposin蛋白亚型PsapE8可以与Rhox5蛋白相结合.To study the interaction between prosaposin with exon 8 isform and Rhox5 protein,the prosaposin cDNA including exon 8 spliced forms was amplified using overlap extension PCR and then was subcloned into pGBKT7 and pGADT7 vectors to construct pGBKT7-Psap^E8 and pGADT7-Psap^E8 plasmids.Yeast two-hybrid assay was used to detect whether Psap^E8 could bind Rhox5 protein in yeast.Psap^E8 proteins was translated in vitro and labeled with 35S-Met using a TNT T7 Quick Coupled transcription/translation reaction kit.GST pull-down was used to confirm the interaction between Psap^E8 and Rhox5 protein in vitro.The recombinant plasmids pGBKT7-Psap^E8 and pGADT7-Psap^E8 were constructed successfully.Yeast two-hybrid assay indicated Psap^E8 could bind RHOX5 in yeast.GST pull-down assay further confirmed this interaction in vitro.The results suggested that Prosaposin with exon 8 isform(Psap^E8) could interact with Rhox5 protein.
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