Wu Ligang, Fan Jihua, Belasco Joel G
Skirball Institute of Biomolecular Medicine and Department of Microbiology, New York University School of Medicine, New York, NY 10016, USA.
Proc Natl Acad Sci U S A. 2006 Mar 14;103(11):4034-9. doi: 10.1073/pnas.0510928103. Epub 2006 Feb 22.
MicroRNAs (miRNAs) are ubiquitous regulators of eukaryotic gene expression. In addition to repressing translation, miRNAs can down-regulate the concentration of mRNAs that contain elements to which they are imperfectly complementary. Using miR-125b and let-7 as representative miRNAs, we show that in mammalian cells this reduction in message abundance is a consequence of accelerated deadenylation, which leads to rapid mRNA decay. The ability of miRNAs to expedite poly(A) removal does not result from decreased translation; nor does translational repression by miRNAs require a poly(A) tail, a 3' histone stem-loop being an effective substitute. These findings suggest that miRNAs use two distinct posttranscriptional mechanisms to down-regulate gene expression.
微小RNA(miRNA)是真核基因表达中普遍存在的调节因子。除了抑制翻译外,miRNA还可以下调含有与其不完全互补元件的mRNA的浓度。以miR-125b和let-7作为代表性miRNA,我们表明在哺乳动物细胞中,这种mRNA丰度的降低是腺苷酸化加速的结果,这导致mRNA快速降解。miRNA加速多聚腺苷酸(poly(A))去除的能力并非源于翻译减少;miRNA介导的翻译抑制也不需要poly(A)尾,3'组蛋白茎环是一种有效的替代物。这些发现表明,miRNA使用两种不同的转录后机制来下调基因表达。