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The role of mammalian poly(A)-binding proteins in co-ordinating mRNA turnover
The function of cytoplasmic PABPs [poly(A)-binding proteins] in promoting mRNA translation has been intensively studied. However, PABPs also have less clearly defined functions in mRNA turnover including roles in default deadenylation, a major rate-limiting step in mRNA decay, as well as roles in th...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3403503/ https://www.ncbi.nlm.nih.gov/pubmed/22817748 http://dx.doi.org/10.1042/BST20120100 |
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author | Brook, Matthew Gray, Nicola K. |
author_facet | Brook, Matthew Gray, Nicola K. |
author_sort | Brook, Matthew |
collection | PubMed |
description | The function of cytoplasmic PABPs [poly(A)-binding proteins] in promoting mRNA translation has been intensively studied. However, PABPs also have less clearly defined functions in mRNA turnover including roles in default deadenylation, a major rate-limiting step in mRNA decay, as well as roles in the regulation of mRNA turnover by cis-acting control elements and in the detection of aberrant mRNA transcripts. In the present paper, we review our current understanding of the complex roles of PABP1 in mRNA turnover, focusing on recent progress in mammals and highlighting some of the major questions that remain to be addressed. |
format | Online Article Text |
id | pubmed-3403503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-34035032012-08-06 The role of mammalian poly(A)-binding proteins in co-ordinating mRNA turnover Brook, Matthew Gray, Nicola K. Biochem Soc Trans Independent Meeting The function of cytoplasmic PABPs [poly(A)-binding proteins] in promoting mRNA translation has been intensively studied. However, PABPs also have less clearly defined functions in mRNA turnover including roles in default deadenylation, a major rate-limiting step in mRNA decay, as well as roles in the regulation of mRNA turnover by cis-acting control elements and in the detection of aberrant mRNA transcripts. In the present paper, we review our current understanding of the complex roles of PABP1 in mRNA turnover, focusing on recent progress in mammals and highlighting some of the major questions that remain to be addressed. Portland Press Ltd. 2012-07-20 2012-08-01 /pmc/articles/PMC3403503/ /pubmed/22817748 http://dx.doi.org/10.1042/BST20120100 Text en © 2012 The Author(s) The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by-nc/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Independent Meeting Brook, Matthew Gray, Nicola K. The role of mammalian poly(A)-binding proteins in co-ordinating mRNA turnover |
title | The role of mammalian poly(A)-binding proteins in co-ordinating mRNA turnover |
title_full | The role of mammalian poly(A)-binding proteins in co-ordinating mRNA turnover |
title_fullStr | The role of mammalian poly(A)-binding proteins in co-ordinating mRNA turnover |
title_full_unstemmed | The role of mammalian poly(A)-binding proteins in co-ordinating mRNA turnover |
title_short | The role of mammalian poly(A)-binding proteins in co-ordinating mRNA turnover |
title_sort | role of mammalian poly(a)-binding proteins in co-ordinating mrna turnover |
topic | Independent Meeting |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3403503/ https://www.ncbi.nlm.nih.gov/pubmed/22817748 http://dx.doi.org/10.1042/BST20120100 |
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