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PMID: 19026789 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Comparative analysis of argonaute-dependent small RNA pathways in Drosophila.

Molecular cell ·Vol. 32 ·No. 4 ·2008-11-21 ·Pages 592-9

Zhou R, Hotta I, Denli AM, Hong P, Perrimon N, Hannon GJ

Abstract

The specificity of RNAi pathways is determined by several classes of small RNAs, which include siRNAs, piRNAs, endo-siRNAs, and microRNAs (miRNAs). These small RNAs are invariably incorporated into large Argonaute (Ago)-containing effector complexes known as RNA-induced silencing complexes (RISCs), which they guide to silencing targets. Both genetic and biochemical strategies have yielded conserved molecular components of small RNA biogenesis and effector machineries. However, given the complexity of these pathways, there are likely to be additional components and regulators that remain to be uncovered. We have undertaken a comparative and comprehensive RNAi screen to identify genes that impact three major Ago-dependent small RNA pathways that operate in Drosophila S2 cells. We identify subsets of candidates that act positively or negatively in siRNA, endo-siRNA, and miRNA pathways. Our studies indicate that many components are shared among all three Argonaute-dependent silencing pathways, though each is also impacted by discrete sets of genes.

MeSH Terms
Animals Argonaute Proteins Cell Line Drosophila/cytology,genetics,metabolism Drosophila Proteins Drosophila melanogaster/genetics,metabolism Eukaryotic Initiation Factors Gene Silencing Genes, Insect MicroRNAs/genetics,metabolism Models, Biological RNA Interference RNA, Small Interfering/genetics,metabolism RNA, Untranslated/genetics,metabolism RNA-Induced Silencing Complex/genetics,metabolism
Chemicals
AGO1 protein, Drosophila AGO2 protein, Drosophila Argonaute Proteins Drosophila Proteins Eukaryotic Initiation Factors MicroRNAs RNA, Small Interfering RNA, Untranslated RNA-Induced Silencing Complex
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Zhou Rui
Department of Genetics, Harvard Medical School, Howard Hughes Medical Institute, Boston, MA 02115, USA.
Hotta Ikuko
Denli Ahmet M
Hong Pengyu
Perrimon Norbert
Hannon Gregory J
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Article Info
Journal
Molecular cell
Abbr.
Mol Cell
ISSN
1097-4164
Published
2008-11-21
Pages
592-9
Language
English
Region
United States
NLM ID
9802571
PMCID
PMC2615197
Subset
IM
Grants
NIBIB NIH HHS · R01 EB007042 · United States
NIGMS NIH HHS · R01 GM062534-06 · United States
NIGMS NIH HHS · R01 GM062534-07 · United States
NIGMS NIH HHS · R01 GM062534 · United States
NIBIB NIH HHS · R01 EB007042-02 · United States
Howard Hughes Medical Institute · United States
NIGMS NIH HHS · R01 GM062534-08 · United States
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