Place Robert F, Li Long-Cheng, Pookot Deepa, Noonan Emily J, Dahiya Rajvir
Department of Urology, Veterans Affairs Medical Center and University of California, San Francisco, CA 94121, USA.
Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1608-13. doi: 10.1073/pnas.0707594105. Epub 2008 Jan 28.
Recent studies have shown that microRNA (miRNA) regulates gene expression by repressing translation or directing sequence-specific degradation of complementary mRNA. Here, we report new evidence in which miRNA may also function to induce gene expression. By scanning gene promoters in silico for sequences complementary to known miRNAs, we identified a putative miR-373 target site in the promoter of E-cadherin. Transfection of miR-373 and its precursor hairpin RNA (pre-miR-373) into PC-3 cells readily induced E-cadherin expression. Knockdown experiments confirmed that induction of E-cadherin by pre-miR-373 required the miRNA maturation protein Dicer. Further analysis revealed that cold-shock domain-containing protein C2 (CSDC2), which possesses a putative miR-373 target site within its promoter, was also readily induced in response to miR-373 and pre-miR-373. Furthermore, enrichment of RNA polymerase II was detected at both E-cadherin and CSDC2 promoters after miR-373 transfection. Mismatch mutations to miR-373 indicated that gene induction was specific to the miR-373 sequence. Transfection of promoter-specific dsRNAs revealed that the concurrent induction of E-cadherin and CSDC2 by miR-373 required the miRNA target sites in both promoters. In conclusion, we have identified a miRNA that targets promoter sequences and induces gene expression. These findings reveal a new mode by which miRNAs may regulate gene expression.
最近的研究表明,微小RNA(miRNA)通过抑制翻译或指导互补mRNA的序列特异性降解来调节基因表达。在此,我们报告了新的证据,表明miRNA也可能具有诱导基因表达的功能。通过在计算机上扫描基因启动子以寻找与已知miRNA互补的序列,我们在E-钙黏蛋白的启动子中鉴定出一个假定的miR-373靶位点。将miR-373及其前体发夹RNA(pre-miR-373)转染到PC-3细胞中可轻易诱导E-钙黏蛋白表达。敲低实验证实,pre-miR-373诱导E-钙黏蛋白表达需要miRNA成熟蛋白Dicer。进一步分析表明,在其启动子内具有假定miR-373靶位点的含冷休克结构域蛋白C2(CSDC2)也能对miR-373和pre-miR-373作出反应而轻易被诱导。此外,miR-373转染后,在E-钙黏蛋白和CSDC2启动子处均检测到RNA聚合酶II的富集。对miR-373的错配突变表明,基因诱导对miR-373序列具有特异性。启动子特异性双链RNA的转染表明,miR-373同时诱导E-钙黏蛋白和CSDC2需要两个启动子中的miRNA靶位点。总之,我们鉴定出了一种靶向启动子序列并诱导基因表达的miRNA。这些发现揭示了miRNA调节基因表达的一种新模式。