Roquin binds microRNA-146a and Argonaute2 to regulate microRNA homeostasis

Date

2015-02-20

Authors

Srivastava, Monika
Duan, Guowen
Kershaw, Nadia J.
Athanasopoulos, Vicki
Yeo, Janet H. C.
Ose, Toyoyuki
Hu, Desheng
Brown, Simon H. J.
Jergic, Slobodan
Patel, Hardip R.

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Nature Publishing Group

Abstract

Roquin is an RNA-binding protein that prevents autoimmunity and inflammation via repression of bound target mRNAs such as inducible costimulator (Icos). When Roquin is absent or mutated (Roquin(san)), Icos is overexpressed in T cells. Here we show that Roquin enhances Dicer-mediated processing of pre-miR-146a. Roquin also directly binds Argonaute2, a central component of the RNA-induced silencing complex, and miR-146a, a microRNA that targets Icos mRNA. In the absence of functional Roquin, miR-146a accumulates in T cells. Its accumulation is not due to increased transcription or processing, rather due to enhanced stability of mature miR-146a. This is associated with decreased 3' end uridylation of the miRNA. Crystallographic studies reveal that Roquin contains a unique HEPN domain and identify the structural basis of the 'san' mutation and Roquin's ability to bind multiple RNAs. Roquin emerges as a protein that can bind Ago2, miRNAs and target mRNAs, to control homeostasis of both RNA species.

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Source

Nature Communications

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Journal article

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