Katoh Takayuki, Sakaguchi Yuriko, Miyauchi Kenjyo, Suzuki Takeo, Kashiwabara Shin-Ichi, Baba Tadashi, Suzuki Tsutomu
Department of Chemistry and Biotechnology, Graduate School of Engineering, University of Tokyo, Bunkyo-ku, Tokyo 113-8656, Japan.
Genes Dev. 2009 Feb 15;23(4):433-8. doi: 10.1101/gad.1761509.
The steady-state levels of microRNAs (miRNAs) and their activities are regulated by the post-transcriptional processes. It is known that 3' ends of several miRNAs undergo post-dicing adenylation or uridylation. We isolated the liver-specific miR-122 from human hepatocytes and mouse livers. Direct analysis by mass spectrometry revealed that one variant of miR-122 has a 3'-terminal adenosine that is introduced after processing by Dicer. We identified GLD-2, which is a regulatory cytoplasmic poly(A) polymerase, as responsible for the 3'-terminal adenylation of miR-122 after unwinding of the miR-122/miR-122* duplex. In livers from GLD-2-null mice, the steady-state level of the mature form of miR-122 was specifically lower than in heterozygous mice, whereas no reduction of pre-miR-122 was observed, demonstrating that 3'-terminal adenylation by GLD-2 is required for the selective stabilization of miR-122 in the liver.
微小RNA(miRNA)的稳态水平及其活性受转录后过程调控。已知几种miRNA的3'末端会发生切割后腺苷化或尿苷化。我们从人肝细胞和小鼠肝脏中分离出肝脏特异性miR-122。质谱直接分析显示,miR-122的一种变体具有一个3'末端腺苷,该腺苷在Dicer加工后引入。我们鉴定出GLD-2,它是一种调节性细胞质聚腺苷酸聚合酶,负责在miR-122/miR-122*双链体解旋后对miR-122进行3'末端腺苷化。在GLD-2基因敲除小鼠的肝脏中,成熟形式的miR-122的稳态水平比杂合小鼠中特异性降低,而未观察到前体miR-122减少,这表明GLD-2介导的3'末端腺苷化是肝脏中miR-122选择性稳定所必需的。