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Gene silencing through RNA interference (RNAi) is carried out by RISC, the RNA-induced silencing complex. RISC contains two signature components, small interfering RNAs (siRNAs) and Argonaute family proteins. Here, we show that the multiple Argonaute proteins present in mammals are both biologically and biochemically distinct, with a single mammalian family member, Argonaute2, being responsible for messenger RNA cleavage activity. This protein is essential for mouse development, and cells lacking Argonaute2 are unable to mount an experimental response to siRNAs. Mutations within a cryptic ribonuclease H domain within Argonaute2, as identified by comparison with the structure of an archeal Argonaute protein, inactivate RISC. Thus, our evidence supports a model in which Argonaute contributes "Slicer" activity to RISC, providing the catalytic engine for RNAi.
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Jidong Liu
Guangxi University
Michelle A. Carmell
University of Massachusetts Chan Medical School
Fabiola V. Rivas
Child Trends
Science
University of North Carolina at Chapel Hill
Stony Brook University
Cold Spring Harbor Laboratory
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Liu et al. (Thu,) studied this question.
synapsesocial.com/papers/6a0cfa0c2e5f14ab7f7c7760 — DOI: https://doi.org/10.1126/science.1102513