摘要
用脂质体介导真核表达质粒pcDNA3-skn-1a转染Hela细胞,实时定量PCR检测HPV18 E6基因的表达量,以探讨转录因子Skn-1a对HPV18 E6基因表达的调控.结果显示Skn-1a能够显著激活HPV18 E6基因表达,为高发宫颈癌E6基因调控的分子机理探讨提供理论依据.
To investigate the regulation of HPV-18 E6 gene expression by skn-1a , HeLa cells were transfected with skn-1a eukaryotic expression plasmid pcDNA3-skn-1a , and the transcription of HPV-18 E6 in HeLa cells was detected with real-time quantitative PCR. The results showed that skn-1a can activate the expression of HPV-18 E6 significantly.
出处
《新疆大学学报(自然科学版)》
CAS
2008年第3期339-342,共4页
Journal of Xinjiang University(Natural Science Edition)
基金
国家自然科学基金资助项目(No.30460008)