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本文引用的文献

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Comparative analysis of argonaute-dependent small RNA pathways in Drosophila.果蝇中依赖于AGO蛋白的小RNA途径的比较分析
Mol Cell. 2008 Nov 21;32(4):592-9. doi: 10.1016/j.molcel.2008.10.018.
2
Drosophila endogenous small RNAs bind to Argonaute 2 in somatic cells.果蝇内源性小RNA在体细胞中与AGO2蛋白结合。
Nature. 2008 Jun 5;453(7196):793-7. doi: 10.1038/nature06938. Epub 2008 May 7.
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An endogenous small interfering RNA pathway in Drosophila.果蝇中的内源性小干扰RNA途径。
Nature. 2008 Jun 5;453(7196):798-802. doi: 10.1038/nature07007. Epub 2008 May 7.
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The Drosophila hairpin RNA pathway generates endogenous short interfering RNAs.果蝇发夹RNA途径可产生内源性小干扰RNA。
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Endogenous siRNAs derived from transposons and mRNAs in Drosophila somatic cells.果蝇体细胞中源自转座子和信使核糖核酸的内源性小干扰核糖核酸。
Science. 2008 May 23;320(5879):1077-81. doi: 10.1126/science.1157396. Epub 2008 Apr 10.
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Getting to the root of miRNA-mediated gene silencing.探寻miRNA介导的基因沉默的根源。
Cell. 2008 Jan 11;132(1):9-14. doi: 10.1016/j.cell.2007.12.024.
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Biogenesis and germline functions of piRNAs.piRNA的生物发生及种系功能
Development. 2008 Jan;135(1):3-9. doi: 10.1242/dev.006486. Epub 2007 Nov 21.
8
Systematic discovery and characterization of fly microRNAs using 12 Drosophila genomes.利用12种果蝇基因组对果蝇微小RNA进行系统发现与特征分析。
Genome Res. 2007 Dec;17(12):1865-79. doi: 10.1101/gr.6593807. Epub 2007 Nov 7.
9
Evolution, biogenesis, expression, and target predictions of a substantially expanded set of Drosophila microRNAs.果蝇微小RNA大量扩增集的进化、生物发生、表达及靶标预测
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10
The Piwi-piRNA pathway provides an adaptive defense in the transposon arms race.Piwi-piRNA 途径在转座子军备竞赛中提供了一种适应性防御。
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果蝇内源性小干扰RNA的加工依赖于一种特定的Loquacious同工型。

Processing of Drosophila endo-siRNAs depends on a specific Loquacious isoform.

作者信息

Zhou Rui, Czech Benjamin, Brennecke Julius, Sachidanandam Ravi, Wohlschlegel James A, Perrimon Norbert, Hannon Gregory J

机构信息

Harvard Medical School, Department of Genetics, Howard Hughes Medical Institute, Boston, Massachusetts 02115, USA.

出版信息

RNA. 2009 Oct;15(10):1886-95. doi: 10.1261/rna.1611309. Epub 2009 Jul 27.

DOI:10.1261/rna.1611309
PMID:19635780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2743050/
Abstract

Drosophila melanogaster expresses three classes of small RNAs, which are classified according to their mechanisms of biogenesis. MicroRNAs are approximately 22-23 nucleotides (nt), ubiquitously expressed small RNAs that are sequentially processed from hairpin-like precursors by Drosha/Pasha and Dcr-1/Loquacious complexes. MicroRNAs usually associate with AGO1 and regulate the expression of protein-coding genes. Piwi-interacting RNAs (piRNAs) of approximately 24-28 nt associate with Piwi-family proteins and can arise from single-stranded precursors. piRNAs function in transposon silencing and are mainly restricted to gonadal tissues. Endo-siRNAs are found in both germline and somatic tissues. These approximately 21-nt RNAs are produced by a distinct Dicer, Dcr-2, and do not depend on Drosha/Pasha complexes. They predominantly bind to AGO2 and target both mobile elements and protein-coding genes. Surprisingly, a subset of endo-siRNAs strongly depend for their production on the dsRNA-binding protein Loquacious (Loqs), thought generally to be a partner for Dcr-1 and a cofactor for miRNA biogenesis. Endo-siRNA production depends on a specific Loqs isoform, Loqs-PD, which is distinct from the one, Loqs-PB, required for the production of microRNAs. Paralleling their roles in the biogenesis of distinct small RNA classes, Loqs-PD and Loqs-PB bind to different Dicer proteins, with Dcr-1/Loqs-PB complexes and Dcr-2/Loqs-PD complexes driving microRNA and endo-siRNA biogenesis, respectively.

摘要

黑腹果蝇表达三类小RNA,它们根据生物合成机制进行分类。微小RNA约为22 - 23个核苷酸(nt),是普遍表达的小RNA,通过Drosha/Pasha和Dcr - 1/Loquacious复合物从发夹状前体依次加工而成。微小RNA通常与AGO1结合并调节蛋白质编码基因的表达。约24 - 28 nt的Piwi相互作用RNA(piRNA)与Piwi家族蛋白结合,可源自单链前体。piRNA在转座子沉默中起作用,主要局限于性腺组织。内源性小干扰RNA(endo - siRNA)存在于生殖系和体细胞组织中。这些约21 nt的RNA由一种独特的Dicer即Dcr - 2产生,且不依赖于Drosha/Pasha复合物。它们主要与AGO2结合,并靶向移动元件和蛋白质编码基因。令人惊讶的是,一部分endo - siRNA的产生强烈依赖于双链RNA结合蛋白Loquacious(Loqs),通常认为它是Dcr - 1的伙伴和微小RNA生物合成的辅助因子。Endo - siRNA的产生依赖于一种特定的Loqs异构体Loqs - PD,它与微小RNA产生所需的Loqs - PB不同。与它们在不同小RNA类别的生物合成中的作用相似,Loqs - PD和Loqs - PB与不同的Dicer蛋白结合,Dcr - 1/Loqs - PB复合物和Dcr - 2/Loqs - PD复合物分别驱动微小RNA和endo - siRNA的生物合成。