DNA-EGS1386胞内诱导核酶P抑制人巨细胞病毒UL49基因的表达  

DNA-EGS1386 in cells induced RNase P inhibits the expression of human cytomegalovirus UL49 gene

作　　者：崔延伟[1] 曾志锋[1] 李弘剑[1] 李月琴[1] 周琪[1] 杨丹[1] 邹奕[1] 杨光[1] 周天鸿[1] 

机构地区：[1]暨南大学生命科学技术学院基因工程药物国家工程研究中心,广州510632

出　　处：《生物工程学报》2009年第11期1690-1696,共7页Chinese Journal of Biotechnology

基　　金：国家自然科学基金(Nos.90608024;30370776);广州市科技攻关项目(No.2006J1-C0111);广东省科技计划项目(No.2006B35502002);广东省自然科学基金重点项目(No.36703);中国博士后科学基金资助项目(No.20080430845)资助~~

摘　　要：外部引导序列(EGSs)是一类与mRNA靶序列互补并能引导核酶P切割靶mRNA的小分子RNA。本实验构建稳定表达UL49基因的HeLa细胞系,设计合成了针对于人巨细胞病毒(HCMV)UL49基因的12ntDNA性质的EGS1386,通过转染稳定表达UL49基因的细胞系,荧光定量PCR和Western blotting检测细胞内目的基因UL49的表达情况。结果显示在DNA-EGS1386作用下UL49基因的表达量降低了50%,表明DNA-EGS1386可以有效引导人的核酶P切割目标mRNA。因此,DNA-EGS可以发展成为一种新的基因沉默技术和潜在的抗病毒试剂。External Guide Sequences（EGSs） represents a novel nucleic acid based gene interference approach to modulate gene expression.They are oligonucleotides that consist of a sequence complementary to a target mRNA and recruit intracellular RNase P for specific degradation of the target RNA.DNA-based EGS1386 with a size of 12 nt was chemically synthesized to target the mRNA coding for the UL49 gene of human cytomegalovirus（HCMV）.The DNA-based EGS1386 molecule efficiently directed human RNase P to cleave the target mRNA sequence in vitro.A reduction of more than 50% in the levels of UL49 expression was observed in human cells treated with the DNA-based EGS1386 targeted UL49 assayed by fluorescent quantization PCR and Western blotting.This results showed that the DNA-EGS1386 can effectively guide the RNase P cut the target mRNA.Therefore,DNA-EGS can develop into a new gene silencing technology and potential of the anti-viral reagents.

关 键 词：短的EGS 基因沉默 UL49基因 核酶P 

分 类 号：R373[医药卫生—病原生物学]