Control of translation and miRNA-dependent repression by a novel poly(A) binding protein, hnRNP-Q.
Translation control often operates via remodeling of messenger ribonucleoprotein particles. The poly(A) binding protein (PABP) simultaneously interacts with the 3' poly(A) tail of the mRNA and the eukaryotic translation initiation factor 4G (eIF4G) to stimulate translation. PABP also promotes m...
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doaj-5d4447b8a6e4451abab1f665007131552021-07-02T13:48:09ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852013-01-01115e100156410.1371/journal.pbio.1001564Control of translation and miRNA-dependent repression by a novel poly(A) binding protein, hnRNP-Q.Yuri V SvitkinAkiko YanagiyaAlexey E KaretnikovTommy AlainMarc R FabianArkady KhoutorskySandra PerreaultIvan TopisirovicNahum SonenbergTranslation control often operates via remodeling of messenger ribonucleoprotein particles. The poly(A) binding protein (PABP) simultaneously interacts with the 3' poly(A) tail of the mRNA and the eukaryotic translation initiation factor 4G (eIF4G) to stimulate translation. PABP also promotes miRNA-dependent deadenylation and translational repression of target mRNAs. We demonstrate that isoform 2 of the mouse heterogeneous nuclear protein Q (hnRNP-Q2/SYNCRIP) binds poly(A) by default when PABP binding is inhibited. In addition, hnRNP-Q2 competes with PABP for binding to poly(A) in vitro. Depleting hnRNP-Q2 from translation extracts stimulates cap-dependent and IRES-mediated translation that is dependent on the PABP/poly(A) complex. Adding recombinant hnRNP-Q2 to the extracts inhibited translation in a poly(A) tail-dependent manner. The displacement of PABP from the poly(A) tail by hnRNP-Q2 impaired the association of eIF4E with the 5' m(7)G cap structure of mRNA, resulting in the inhibition of 48S and 80S ribosome initiation complex formation. In mouse fibroblasts, silencing of hnRNP-Q2 stimulated translation. In addition, hnRNP-Q2 impeded let-7a miRNA-mediated deadenylation and repression of target mRNAs, which require PABP. Thus, by competing with PABP, hnRNP-Q2 plays important roles in the regulation of global translation and miRNA-mediated repression of specific mRNAs.http://europepmc.org/articles/PMC3660254?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yuri V Svitkin Akiko Yanagiya Alexey E Karetnikov Tommy Alain Marc R Fabian Arkady Khoutorsky Sandra Perreault Ivan Topisirovic Nahum Sonenberg |
spellingShingle |
Yuri V Svitkin Akiko Yanagiya Alexey E Karetnikov Tommy Alain Marc R Fabian Arkady Khoutorsky Sandra Perreault Ivan Topisirovic Nahum Sonenberg Control of translation and miRNA-dependent repression by a novel poly(A) binding protein, hnRNP-Q. PLoS Biology |
author_facet |
Yuri V Svitkin Akiko Yanagiya Alexey E Karetnikov Tommy Alain Marc R Fabian Arkady Khoutorsky Sandra Perreault Ivan Topisirovic Nahum Sonenberg |
author_sort |
Yuri V Svitkin |
title |
Control of translation and miRNA-dependent repression by a novel poly(A) binding protein, hnRNP-Q. |
title_short |
Control of translation and miRNA-dependent repression by a novel poly(A) binding protein, hnRNP-Q. |
title_full |
Control of translation and miRNA-dependent repression by a novel poly(A) binding protein, hnRNP-Q. |
title_fullStr |
Control of translation and miRNA-dependent repression by a novel poly(A) binding protein, hnRNP-Q. |
title_full_unstemmed |
Control of translation and miRNA-dependent repression by a novel poly(A) binding protein, hnRNP-Q. |
title_sort |
control of translation and mirna-dependent repression by a novel poly(a) binding protein, hnrnp-q. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Biology |
issn |
1544-9173 1545-7885 |
publishDate |
2013-01-01 |
description |
Translation control often operates via remodeling of messenger ribonucleoprotein particles. The poly(A) binding protein (PABP) simultaneously interacts with the 3' poly(A) tail of the mRNA and the eukaryotic translation initiation factor 4G (eIF4G) to stimulate translation. PABP also promotes miRNA-dependent deadenylation and translational repression of target mRNAs. We demonstrate that isoform 2 of the mouse heterogeneous nuclear protein Q (hnRNP-Q2/SYNCRIP) binds poly(A) by default when PABP binding is inhibited. In addition, hnRNP-Q2 competes with PABP for binding to poly(A) in vitro. Depleting hnRNP-Q2 from translation extracts stimulates cap-dependent and IRES-mediated translation that is dependent on the PABP/poly(A) complex. Adding recombinant hnRNP-Q2 to the extracts inhibited translation in a poly(A) tail-dependent manner. The displacement of PABP from the poly(A) tail by hnRNP-Q2 impaired the association of eIF4E with the 5' m(7)G cap structure of mRNA, resulting in the inhibition of 48S and 80S ribosome initiation complex formation. In mouse fibroblasts, silencing of hnRNP-Q2 stimulated translation. In addition, hnRNP-Q2 impeded let-7a miRNA-mediated deadenylation and repression of target mRNAs, which require PABP. Thus, by competing with PABP, hnRNP-Q2 plays important roles in the regulation of global translation and miRNA-mediated repression of specific mRNAs. |
url |
http://europepmc.org/articles/PMC3660254?pdf=render |
work_keys_str_mv |
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