| Literature DB >> 23195953 |
Jacqueline Baca LeGendre1, Zachary T Campbell, Peggy Kroll-Conner, Phil Anderson, Judith Kimble, Marvin Wickens.
Abstract
The Staufen family consists of proteins that possess double-stranded RNA-binding domains (dsRBDs). Staufen proteins of Drosophila and mammals regulate mRNA localization, translation, and decay. We report analysis of Staufen in Caenorhabditis elegans, which we have designated STAU-1. We focus on its biochemical properties, mRNA targets, and possible role in RNAi. We show that STAU-1 is expressed as mRNA and protein at all stages of C. elegans development. The wild-type, full-length protein, purified from bacteria, binds duplex RNA with high affinity in vitro. Purified, mutant proteins lacking single dsRBDs still bind RNA efficiently, demonstrating that no single domain is required for binding to duplex RNA (although dsRBD2 could not be tested). STAU-1 mRNA targets were identified via immunoprecipitation with specific anti-STAU-1 antibodies, followed by microarray analysis (RIP-Chip). These studies define a set of 418 likely STAU-1 mRNA targets. Finally, we demonstrate that stau-1 mutants enhance exogenous RNAi and that stau-1;eri-1 double mutants exhibit sterility and synthetic germ line defects.Entities:
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Year: 2012 PMID: 23195953 PMCID: PMC3554921 DOI: 10.1074/jbc.M112.397349
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157