Tao Guang-shi, Zhang Ke-qiang, Chen Yong, Nie Mei-fang, Liu Feng-ying, Wu Yi-lin, Liu Yi-zhi, Wu Xiu-shan
Department of Gynecology, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhonghua Fu Chan Ke Za Zhi. 2005 Oct;40(10):693-6.
To investigate the inhibition of HPV18E6 gene in HeLa cell transfected with plasmid expressing human papilloma virus 18 E6 (HPV18E6) short hairpin RNA (shRNA).
We synthesized two HPV18E6 shRNA frames and sub-cloned them into pSUPER which can express shRNA in mammalian cells to construct pE6-1shRNA and pE6-2shRNA which were mutant in E6 shRNA frame. The pE6-1shRNA, pE6-2shRNA and pcDNA3.1 were co-transfected into HeLa cells by cationic liposome respectively and the positive transfectants were selected by G418. The HPV18E6 mRNA and protein expression level was detected by semi-quantitative RT-PCR and streptavidin-peroxidase conjugated method (SP) to assay the inhibitory effects of pE6shRNA.
We successfully constructed several new HeLa cell lines transfected with pE6-1shRNA and pE6-2shRNA. In the HeLa cells without transfection and the HeLa cells transfected with pE6-1shRNA plasmid, the HPV18E6 mRNA levels were 1.14 +/- 0.45, 0.76 +/- 0.28 respectively, and the difference of HPV18E6 mRNA levels was significant (P < 0.05). The inhibition efficiency of HPV18E6 gene mRNA was 33.3% and the HPV18E6 protein levels were declined after transfection with pE6-1shRNA. In the HeLa cells transfected with pE6-2shRNA and pSUPER plasmids, HPV18E6 mRNA and protein expression levels were not different from those in wild HeLa cells.
The pE6-1shRNA plasmid can inhibit HPV18E6 expression in HeLa cells, which is persistent, specific and heritable.
研究表达人乳头瘤病毒18 E6(HPV18E6)短发夹RNA(shRNA)的质粒转染HeLa细胞后对HPV18E6基因的抑制作用。
合成两条HPV18E6 shRNA框架,并将其亚克隆至可在哺乳动物细胞中表达shRNA的pSUPER载体,构建E6 shRNA框架发生突变的pE6 - 1shRNA和pE6 - 2shRNA。将pE6 - 1shRNA、pE6 - 2shRNA和pcDNA3.1分别通过阳离子脂质体共转染入HeLa细胞,并用G418筛选阳性转染子。采用半定量逆转录 - 聚合酶链反应(RT - PCR)和链霉亲和素 - 过氧化物酶偶联法(SP)检测HPV18E6 mRNA和蛋白表达水平,以分析pE6shRNA的抑制效果。
成功构建了多个转染pE6 - 1shRNA和pE6 - 2shRNA的HeLa细胞新株系。未转染的HeLa细胞和转染pE6 - 1shRNA质粒的HeLa细胞中,HPV18E6 mRNA水平分别为1.14±0.45、0.76±0.28,HPV18E6 mRNA水平差异有统计学意义(P < 0.05)。转染pE6 - 1shRNA后,HPV18E6基因mRNA的抑制效率为33.3%,且HPV18E6蛋白水平下降。转染pE6 - 2shRNA和pSUPER质粒的HeLa细胞中,HPV18E6 mRNA和蛋白表达水平与野生型HeLa细胞无差异。
pE6 - 1shRNA质粒可抑制HeLa细胞中HPV18E6的表达,且具有持续性、特异性和遗传性。