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首页> 外文期刊>Nature structural & molecular biology >LIN-28 and the poly(U) polymerase PUP-2 regulate let-7 microRNA processing in Caenorhabditis elegans
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LIN-28 and the poly(U) polymerase PUP-2 regulate let-7 microRNA processing in Caenorhabditis elegans

机译:LIN-28和poly(U)聚合酶PUP-2调节秀丽隐杆线虫中let-7 microRNA的加工

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The let-7 microRNA ( miRNA) is an ultraconserved regulator of stem cell differentiation and developmental timing and a candidate tumor suppressor. Here we show that LIN-28 and the poly( U) polymerase PUP-2 regulate let-7 processing in Caenorhabditis elegans. We demonstrate that lin-28 is necessary and sufficient to block let-7 activity in vivo; LIN-28 directly binds let-7 pre-miRNA to prevent Dicer processing. Moreover, we have identified a poly( U) polymerase, PUP-2, which regulates the stability of LIN-28 blockaded let-7 pre-miRNA and contributes to LIN-28-dependent regulation of let-7 during development. We show that PUP-2 and LIN-28 interact directly, and that LIN-28 stimulates uridylation of let-7 pre-miRNA by PUP-2 in vitro. Our results demonstrate that LIN-28 and let-7 form an ancient regulatory switch, conserved from nematodes to humans, and provide insight into the mechanism of LIN-28 action in vivo. Uridylation by a PUP-2 ortholog might regulate let-7 and additional miRNAs in other species. Given the roles of Lin28 and let-7 in stem cell and cancer biology, we propose that such poly( U) polymerases are potential therapeutic targets.
机译:let-7 microRNA(miRNA)是干细胞分化和发育时间的超保守调节剂,也是候选的肿瘤抑制因子。在这里,我们显示LIN-28和poly(U)聚合酶PUP-2调节秀丽隐杆线虫中的let-7加工。我们证明lin-28是必要的,并且足以阻止let-7的体内活性。 LIN-28直接结合let-7 pre-miRNA,以防止Dicer加工。此外,我们已经确定了一种聚(U)聚合酶PUP-2,它调节LIN-28阻断的let-7 pre-miRNA的稳定性,并在发育过程中对LIN-28依赖性的let-7作出贡献。我们表明,PUP-2和LIN-28直接相互作用,并且LIN-28刺激PUP-2在体外对let-7 pre-miRNA的尿苷化。我们的结果表明,LIN-28和let-7形成了古老的调节开关,从线虫到人类都是保守的,并提供了对LIN-28体内作用机制的深入了解。 PUP-2直系同源物的Uridylation可能调节let-7和其他物种的其他miRNA。鉴于Lin28和let-7在干细胞和癌症生物学中的作用,我们建议此类poly(U)聚合酶是潜在的治疗靶标。

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