酵母组蛋白乙酰基转移酶GCN5和去乙酰化酶RPD3在大肠杆菌中的表达  

Cloning and Prokaryotic Expression of Yeast GCN5 and RPD3

作　　者：陈婷[1] 陆军[1] 孙晖[1] 董梅[1] 韩松岩[1] 黄百渠[1] 

机构地区：[1]东北师范大学遗传与细胞研究所,长春130024

出　　处：《遗传》2003年第5期567-572,共6页Hereditas（Beijing)

基　　金：国家自然科学基金项目(39970384);国家"973"计划项目(G1999053902)资助

摘　　要：以酵母基因组DNA为模板,通过PCR方法分别扩增出在5′端带有6xHis标签的gcn5和rpd3基因,将其克隆到pBV220质粒中,分别构建成表达质粒pBVgcn5和pBVrpd3,转化大肠杆菌(Escherichiacoli)并进行诱导表达。SDS PAGE显示,含重组质粒的菌株经热诱导后分别过量表达出约50kDa的蛋白。利用6xHis亲和层析纯化了这两种重组酶。对组蛋白乙酰基转移酶GCN5进行体外活性检测,证实其具有组蛋白乙酰基转移酶活性。本工作为通过体外实验研究乙酰化和去乙酰化修饰与基因转录调控的关系奠定了基础。The yeast histone acetyltransferase (HAT) gene gcn5 and histone deacetylase (HDAC) gene rpd3 were cloned from yeast genomic DNA by PCR amplification.The two genes,both with additional 6xHis tag,were subcloned into pBV220 vector to construct expression plasmids pBVgcn5 and pBVrpd3,respectively.Both pBVgcn5 and pBVrpd3 were overexpressed in Escherichia coli upon temperature induction,as revealed by SDSPAGE.The recombinant GCN5 and RPD3 were purified by using a 6xHis affinity column.The purified GCN5 was tested to possess the HAT activity by using a 14Clabeling assay.This work has laid down the basis for further in vitro studies into roles of histone acetylation/deacetylation in modulating chromatin conformation and transcription activity.

关 键 词：组蛋白乙酰基转移酶 组蛋白去乙酰化酶 GCN5 RPD3 基因克隆 大肠杆菌 表达 

分 类 号：Q786[生物学—分子生物学]