Sato Mari M, Nashimoto Masayuki, Katagiri Takenobu, Yawaka Yasutaka, Tamura Masato
Department of Biochemistry and Molecular Biology, Hokkaido University, Sapporo, Japan.
Biochem Biophys Res Commun. 2009 May 22;383(1):125-9. doi: 10.1016/j.bbrc.2009.03.142. Epub 2009 Mar 31.
MicroRNAs (miRNAs) are small non-coding RNAs that are emerging as important post-transcriptional gene regulators. miR-206 is unique in that it is expressed only in skeletal muscle, including the myoblastic C2C12 cell line. In C2C12 cells, miR-206 expression was reduced dramatically after bone morphogenetic protein (BMP)-2 treatment. The down-regulation of miR-206 expression was also observed after co-transfection with constitutively-active Smad1 and Smad4, which are the intracellular signaling molecules of the BMP pathway. BMP-2 also reduced miR-206 expression in the presence of alpha-amanitin in a similar manner to that in the absence of alpha-amanitin. Moreover, the expression of pri-miR-206 was increased upon BMP-2 treatment for 6h compared to that in the absence of BMP-2. These results suggested that BMP-2 down-regulates miR-206 expression at the post-transcriptional level, by inhibiting the processing of pri-miR-206 into mature miR-206, and that BMP-2 could regulate miRNA biogenesis by a novel mechanism.
微小RNA(miRNA)是一类小型非编码RNA,正逐渐成为重要的转录后基因调节因子。miR-206的独特之处在于它仅在骨骼肌中表达,包括成肌C2C12细胞系。在C2C12细胞中,骨形态发生蛋白(BMP)-2处理后miR-206的表达显著降低。与组成型激活的Smad1和Smad4(BMP途径的细胞内信号分子)共转染后,也观察到miR-206表达的下调。在存在α-鹅膏蕈碱的情况下,BMP-2也以与不存在α-鹅膏蕈碱时类似的方式降低miR-206的表达。此外,与未用BMP-2处理相比,BMP-2处理6小时后pri-miR-206的表达增加。这些结果表明,BMP-2通过抑制pri-miR-206加工成成熟miR-206,在转录后水平下调miR-206的表达,并且BMP-2可能通过一种新机制调节miRNA的生物合成。