Li Zhao-lun, Xu Wu-jun, Tian Pu-xun, Ding Xiao-ming, Tian Xiao-hui, Feng Xin-shun, Hou Jun
Department of Kidney Transplantation, First Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an 710061, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2007 Sep;27(9):1299-302.
To construct a replication-incompetent recombinant adenovirus mediating short hairpin RNA (shRNA)-induced tissue factor gene silencing in the islet.
Four pairs of complementary oligonucleotides were designed and synthesized to create double-stranded oligonucleotides (ds oligo). The ds oligos were cloned into Pentr/U6 vector to construct the shuttle plasmid pENTR/U6-shRNA, which was transduced into human islets via liposome after sequence verification. The plasmid with the best silencing effect was identified by real-time RT-PCR, followed by homologous recombination with the adenovirus backbone plasmid. The functional clone was transfected into 293A cells to amplify the adenovirus, whose silencing effect against TF expression was tested using real-time RT-PCR and Western blotting.
The pENTR/U6-shRNA shuttle plasmid was constructed and verified by sequencing. The recombinant adenovirus-mediated shRNA against TF was constructed, and real-time RT-PCR and Western blotting demonstrated that the strongest silencing effect of the adenovirus against TF occurred on the 4th day following islet transfection.
Replication-incompetent recombinant adenovirus-mediated shRNA against TF has been successfully constructed, which has good silencing effect against TF expression in human islet in vitro.
构建一种无复制能力的重组腺病毒,介导短发夹RNA(shRNA)诱导胰岛组织因子基因沉默。
设计并合成四对互补寡核苷酸以产生双链寡核苷酸(ds oligo)。将ds oligo克隆到Pentr/U6载体中构建穿梭质粒pENTR/U6-shRNA,经序列验证后通过脂质体转导入人胰岛。通过实时RT-PCR鉴定沉默效果最佳的质粒,随后与腺病毒骨架质粒进行同源重组。将功能克隆转染至293A细胞以扩增腺病毒,使用实时RT-PCR和蛋白质印迹法检测其对TF表达的沉默效果。
构建了pENTR/U6-shRNA穿梭质粒并经测序验证。构建了重组腺病毒介导的针对TF的shRNA,实时RT-PCR和蛋白质印迹法表明,腺病毒对TF的最强沉默效果出现在胰岛转染后的第4天。
已成功构建无复制能力的重组腺病毒介导的针对TF的shRNA,其在体外对人胰岛中TF表达具有良好的沉默效果。