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通过类Dicer 1蛋白功能实现拟南芥微小RNA的生物合成

Arabidopsis micro-RNA biogenesis through Dicer-like 1 protein functions.

作者信息

Kurihara Yukio, Watanabe Yuichiro

机构信息

Department of Life Sciences, Graduate School of Arts and Sciences, University of Tokyo, Komaba 3-8-1, Meguro-ku, Tokyo 153-8902, Japan.

出版信息

Proc Natl Acad Sci U S A. 2004 Aug 24;101(34):12753-8. doi: 10.1073/pnas.0403115101. Epub 2004 Aug 16.

DOI:10.1073/pnas.0403115101
PMID:15314213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC515125/
Abstract

Micro-RNAs (miRNAs) are small, noncoding RNAs of 18-25 nt in length that negatively regulate their complementary mRNAs at the posttranscriptional level. Previous work has shown that some RNase III-like enzymes such as Drosha and Dicer are known to be involved in miRNA biogenesis in animals. However, the mechanism of plant miRNA biogenesis still remains poorly understood. In this article, the process of Arabidopsis miR163 biogenesis was examined. The results revealed that two types of miR163 primary transcripts (pri-miR163s) are transcribed from a single gene by RNA polymerase II and that miR163 biogenesis requires at least three cleavage steps by RNase III-like enzymes at 21-nt-long intervals. The first step is from pri-miR163 to long miR163 precursor (premiR163), the second step is from long pre-miR163 to short premiR163, and the last step is from short pre-miR163 to mature miR163 and the remnant. It is interesting that, during the process, four small RNAs including miR163 are released. By using dcl1 mutants, it was demonstrated that Arabidopsis Dicer homologue Dicer-like 1 (DCL1) catalyzes at least the first and second cleavage steps and that double-stranded RNA-binding domains of DCL1 are involved in positioning of the cleavage sites. Our result is direct evidence that DCL1 is involved in processing of pri- and pre-miRNA.

摘要

微小RNA(miRNA)是长度为18 - 25个核苷酸的小型非编码RNA,它们在转录后水平对其互补mRNA进行负调控。先前的研究表明,一些核糖核酸酶III样酶,如Drosha和Dicer,参与动物体内的miRNA生物合成。然而,植物miRNA生物合成的机制仍知之甚少。在本文中,对拟南芥miR163的生物合成过程进行了研究。结果显示,两种类型的miR163初级转录本(pri - miR163)由RNA聚合酶II从单个基因转录而来,并且miR163的生物合成需要核糖核酸酶III样酶以21个核苷酸的间隔进行至少三个切割步骤。第一步是从pri - miR163到长miR163前体(pre - miR163),第二步是从长pre - miR163到短pre - miR163,最后一步是从短pre - miR163到成熟miR163及其残余物。有趣的是,在此过程中会释放包括miR163在内的四种小RNA。通过使用dcl1突变体,证明拟南芥Dicer同源物Dicer - like 1(DCL1)至少催化第一步和第二步切割,并且DCL1的双链RNA结合结构域参与切割位点的定位。我们的结果直接证明DCL1参与pri - miRNA和pre - miRNA的加工。

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Cross-protection in Arabidopsis against crucifer tobamovirus Cg by an attenuated strain of the virus.通过病毒的减毒株在拟南芥中对十字花科烟草花叶病毒 Cg 的交叉保护。
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