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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