CBC-ARS2 stimulates 3′-end maturation of multiple RNA families and favors cap-proximal processing

被引:130
作者
Hallais, Marie [1 ]
Pontvianne, Frederic [1 ]
Andersen, Peter Refsing [2 ]
Clerici, Marcello [3 ]
Lener, Daniela [1 ]
Benbahouche, Nour El Houda [1 ]
Gostan, Thierry [1 ]
Vandermoere, Franck [4 ]
Robert, Marie-Cecile [1 ]
Cusack, Stephen [3 ]
Verheggen, Celine [1 ]
Jensen, Torben Heick [2 ]
Bertrand, Edouard [1 ]
机构
[1] CNRS, Inst Genet Mol Montpellier, Equipe Labellisee Ligue Canc, Montpellier, France
[2] Aarhus Univ, Dept Mol Biol & Genet, Ctr mRNP Biogenesis & Metab, Aarhus, Denmark
[3] European Mol Biol Lab Grenoble Outstn, Grenoble, France
[4] CNRS, Inst Genom Fonct, Montpellier, France
基金
新加坡国家研究基金会;
关键词
PRE-MESSENGER-RNA; BINDING COMPLEX; 3' END; U1; SNRNP; TERMINAL DOMAIN; PROTEIN; EXPORT; INTERACTS; PHOSPHORYLATION; INTEGRATOR;
D O I
10.1038/nsmb.2720
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The nuclear cap-binding complex (CBC) stimulates multiple steps in several RNA maturation pathways, but how it functions in humans is incompletely understood. For small, capped RNAs such as pre-snRNAs, the CBC recruits PHAX. Here, we identify the CBCAP complex, composed of CBC, ARS2 and PHAX, and show that both CBCAP and CBC ARS2 complexes can be reconstituted from recombinant proteins. ARS2 stimulates PHAX binding to the CBC and snRNA 3'-end processing, thereby coupling maturation with export. In vivo, CBC and ARS2 bind similar capped noncoding and coding RNAs and stimulate their 3'-end processing. The strongest effects are for cap-proximal polyadenylation sites, and this favors premature transcription termination. ARS2 functions partly through the mRNA 3'-end cleavage factor CLP1, which binds RNA Polymerase II through PCF11. ARS2 is thus a major CBC effector that stimulates functional and cryptic 3'-end processing sites.
引用
收藏
页码:1358 / 1366
页数:9
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