重组干扰质粒对卵巢癌COC1细胞HDAC1表达的影响  

Interference recombinant plasmids targeting HDAC1 gene in ovarian cancer cell COC1

作　　者：贾妍[1] 邹颖刚[1] 许天敏[1] 崔满华[1] JIA Yan ZOU Ying-gang XU Tian-min et al.(Department of Obstetrics and Gynecology, Second Hospital of Jilin University ,Changchun 130041, China)

机构地区：[1]吉林大学第二医院妇产科,吉林长春130041

出　　处：《中国实验诊断学》2016年第10期1615-1618,共4页Chinese Journal of Laboratory Diagnosis

基　　金：吉林省科技厅青年科研基金(201201034)

摘　　要：目的构建重组HDAC1基因的短发夹RNA(shRNA)慢病毒干扰质粒并研究其对卵巢癌COC1细胞HDAC1表达的影响。方法针对HDAC1基因设计特异性siRNA靶点,构建慢病毒干扰质粒载体,筛选获得的有效shRNA慢病毒干扰序列,将其转染卵巢癌COC1细胞。采用Real-time PCR方法检测靶基因在mRNA水平的沉默效果,Western blot方法检测靶基因在蛋白质水平的沉默效果。结果构建的慢病毒载体shRNA的PCR鉴定和测序正确。shRNA慢病毒干扰质粒转染COC1细胞后HDAC1基因的mRNA表达量和蛋白质水平较阴性对照质粒转染组均显著下调(P<0.05)。结论成功构建HDAC1基因的shRNA慢病毒干扰质粒,该慢病毒干扰质粒能够在细胞水平有效沉默靶基因。Objective To construct the shRNA lentiviral plasmid targeting HDAC1 gene and detect its effect of gene silence in COC1 cells.Methods The specific siRNA sequences targeting HDAC1 gene were cloned into pRNAT-U6.2/Lenti lentiviral plasmid.After screening for the valid siRNA,HDAC1 specific shRNA was transfectted into COC1 cells.Then,real-time PCR and Western Blot was performed to determine the expression level of HDAC1.ResultsPCR and sequencing results revealed that shRNA plasmids were correctly constructed.The HDAC1 expressions in COC1 cells were down regulated at mRNA and protein level by plasmid transfection.The expression of HDAC1 was decreased in mRNA levels and protein compared with negative control.Conclusion The recombinant lentiviral shRNA plasmid targeting HDAC1 gene has been successfully constructed.HDAC1 mRNA and protein can be down-regulated availably in COC1 cells.

关 键 词：HDAC1 短发夹RNA 慢病毒 

分 类 号：R737.31[医药卫生—肿瘤]