作者
Thomas F Duchaine, James A Wohlschlegel, Scott Kennedy, Yanxia Bei, Darryl Conte, KaMing Pang, Daniel R Brownell, Sandra Harding, Shohei Mitani, Gary Ruvkun, John R Yates, Craig C Mello
发表日期
2006/1/27
期刊
Cell
卷号
124
期号
2
页码范围
343-354
出版商
Elsevier
简介
In plants, animals, and fungi, members of the Dicer family of RNase III-related enzymes process double-stranded RNA (dsRNA) to initiate small-RNA-mediated gene-silencing mechanisms. To learn how C. elegans Dicer, DCR-1, functions in multiple distinct silencing mechanisms, we used a mass-spectrometry-based proteomics approach to identify DCR-1-interacting proteins. We then generated and characterized deletion alleles for the corresponding genes. The interactors are required for production of three species of small RNA, including (1) small interfering RNAs (siRNAs), derived from exogenous dsRNA triggers (exo-siRNAs); (2) siRNAs derived from endogenous triggers (endo-siRNAs); and (3) developmental regulatory microRNAs (miRNAs). One interactor, the conserved RNA-phosphatase homolog PIR-1, is required for the processing of a putative amplified DCR-1 substrate. Interactors required for endo …
引用总数
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