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Analysis of mRNA deadenylation by multi-protein complexes

Poly(A) tails are found at the 3′ end of almost every eukaryotic mRNA and are important for the stability of mRNAs and their translation into proteins. Thus, removal of the poly(A) tail, a process called deadenylation, is critical for regulation of gene expression. Most deadenylation enzymes are com...

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Detalles Bibliográficos
Autores principales: Webster, Michael W., Stowell, James A.W., Tang, Terence T.L., Passmore, Lori A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595164/
https://www.ncbi.nlm.nih.gov/pubmed/28624538
http://dx.doi.org/10.1016/j.ymeth.2017.06.009
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author Webster, Michael W.
Stowell, James A.W.
Tang, Terence T.L.
Passmore, Lori A.
author_facet Webster, Michael W.
Stowell, James A.W.
Tang, Terence T.L.
Passmore, Lori A.
author_sort Webster, Michael W.
collection PubMed
description Poly(A) tails are found at the 3′ end of almost every eukaryotic mRNA and are important for the stability of mRNAs and their translation into proteins. Thus, removal of the poly(A) tail, a process called deadenylation, is critical for regulation of gene expression. Most deadenylation enzymes are components of large multi-protein complexes. Here, we describe an in vitro deadenylation assay developed to study the exonucleolytic activities of the multi-protein Ccr4-Not and Pan2-Pan3 complexes. We discuss how this assay can be used with short synthetic RNAs, as well as longer RNA substrates generated using in vitro transcription. Importantly, quantitation of the reactions allows detailed analyses of deadenylation in the presence and absence of accessory factors, leading to new insights into targeted mRNA decay.
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spelling pubmed-55951642017-09-20 Analysis of mRNA deadenylation by multi-protein complexes Webster, Michael W. Stowell, James A.W. Tang, Terence T.L. Passmore, Lori A. Methods Article Poly(A) tails are found at the 3′ end of almost every eukaryotic mRNA and are important for the stability of mRNAs and their translation into proteins. Thus, removal of the poly(A) tail, a process called deadenylation, is critical for regulation of gene expression. Most deadenylation enzymes are components of large multi-protein complexes. Here, we describe an in vitro deadenylation assay developed to study the exonucleolytic activities of the multi-protein Ccr4-Not and Pan2-Pan3 complexes. We discuss how this assay can be used with short synthetic RNAs, as well as longer RNA substrates generated using in vitro transcription. Importantly, quantitation of the reactions allows detailed analyses of deadenylation in the presence and absence of accessory factors, leading to new insights into targeted mRNA decay. Academic Press 2017-08-15 /pmc/articles/PMC5595164/ /pubmed/28624538 http://dx.doi.org/10.1016/j.ymeth.2017.06.009 Text en © 2017 MRC Laboratory of Molecular Biology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Webster, Michael W.
Stowell, James A.W.
Tang, Terence T.L.
Passmore, Lori A.
Analysis of mRNA deadenylation by multi-protein complexes
title Analysis of mRNA deadenylation by multi-protein complexes
title_full Analysis of mRNA deadenylation by multi-protein complexes
title_fullStr Analysis of mRNA deadenylation by multi-protein complexes
title_full_unstemmed Analysis of mRNA deadenylation by multi-protein complexes
title_short Analysis of mRNA deadenylation by multi-protein complexes
title_sort analysis of mrna deadenylation by multi-protein complexes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595164/
https://www.ncbi.nlm.nih.gov/pubmed/28624538
http://dx.doi.org/10.1016/j.ymeth.2017.06.009
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