Functional Genomic Analysis of RNA Interference in C. elegans

Author:

Kim John K.12345,Gabel Harrison W.12345,Kamath Ravi S.12345,Tewari Muneesh12345,Pasquinelli Amy12345,Rual Jean-François12345,Kennedy Scott12345,Dybbs Michael12345,Bertin Nicolas12345,Kaplan Joshua M.12345,Vidal Marc12345,Ruvkun Gary12345

Affiliation:

1. Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA.

2. Department of Genetics, Harvard Medical School, Boston, MA 02114, USA.

3. Center for Cancer Systems Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

4. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

5. Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

Abstract

RNA interference (RNAi) of target genes is triggered by double-stranded RNAs (dsRNAs) processed by conserved nucleases and accessory factors. To identify the genetic components required for RNAi, we performed a genome-wide screen using an engineered RNAi sensor strain of Caenorhabditis elegans . The RNAi screen identified 90 genes. These included Piwi/PAZ proteins, DEAH helicases, RNA binding/processing factors, chromatin-associated factors, DNA recombination proteins, nuclear import/export factors, and 11 known components of the RNAi machinery. We demonstrate that some of these genes are also required for germline and somatic transgene silencing. Moreover, the physical interactions among these potential RNAi factors suggest links to other RNA-dependent gene regulatory pathways.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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