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Trans‐acting translational regulatory RNA binding proteins

The canonical molecular machinery required for global mRNA translation and its control has been well defined, with distinct sets of proteins involved in the processes of translation initiation, elongation and termination. Additionally, noncanonical, trans‐acting regulatory RNA‐binding proteins (RBPs...

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Autores principales: Harvey, Robert F., Smith, Tom S., Mulroney, Thomas, Queiroz, Rayner M. L., Pizzinga, Mariavittoria, Dezi, Veronica, Villenueva, Eneko, Ramakrishna, Manasa, Lilley, Kathryn S., Willis, Anne E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947564/
https://www.ncbi.nlm.nih.gov/pubmed/29341429
http://dx.doi.org/10.1002/wrna.1465
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author Harvey, Robert F.
Smith, Tom S.
Mulroney, Thomas
Queiroz, Rayner M. L.
Pizzinga, Mariavittoria
Dezi, Veronica
Villenueva, Eneko
Ramakrishna, Manasa
Lilley, Kathryn S.
Willis, Anne E.
author_facet Harvey, Robert F.
Smith, Tom S.
Mulroney, Thomas
Queiroz, Rayner M. L.
Pizzinga, Mariavittoria
Dezi, Veronica
Villenueva, Eneko
Ramakrishna, Manasa
Lilley, Kathryn S.
Willis, Anne E.
author_sort Harvey, Robert F.
collection PubMed
description The canonical molecular machinery required for global mRNA translation and its control has been well defined, with distinct sets of proteins involved in the processes of translation initiation, elongation and termination. Additionally, noncanonical, trans‐acting regulatory RNA‐binding proteins (RBPs) are necessary to provide mRNA‐specific translation, and these interact with 5′ and 3′ untranslated regions and coding regions of mRNA to regulate ribosome recruitment and transit. Recently it has also been demonstrated that trans‐acting ribosomal proteins direct the translation of specific mRNAs. Importantly, it has been shown that subsets of RBPs often work in concert, forming distinct regulatory complexes upon different cellular perturbation, creating an RBP combinatorial code, which through the translation of specific subsets of mRNAs, dictate cell fate. With the development of new methodologies, a plethora of novel RNA binding proteins have recently been identified, although the function of many of these proteins within mRNA translation is unknown. In this review we will discuss these methodologies and their shortcomings when applied to the study of translation, which need to be addressed to enable a better understanding of trans‐acting translational regulatory proteins. Moreover, we discuss the protein domains that are responsible for RNA binding as well as the RNA motifs to which they bind, and the role of trans‐acting ribosomal proteins in directing the translation of specific mRNAs. 1.. RNA Interactions with Proteins and Other Molecules > RNA–Protein Complexes; 2.. Translation > Translation Regulation; 3.. Translation > Translation Mechanisms;
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spelling pubmed-59475642018-05-17 Trans‐acting translational regulatory RNA binding proteins Harvey, Robert F. Smith, Tom S. Mulroney, Thomas Queiroz, Rayner M. L. Pizzinga, Mariavittoria Dezi, Veronica Villenueva, Eneko Ramakrishna, Manasa Lilley, Kathryn S. Willis, Anne E. Wiley Interdiscip Rev RNA Advanced Reviews The canonical molecular machinery required for global mRNA translation and its control has been well defined, with distinct sets of proteins involved in the processes of translation initiation, elongation and termination. Additionally, noncanonical, trans‐acting regulatory RNA‐binding proteins (RBPs) are necessary to provide mRNA‐specific translation, and these interact with 5′ and 3′ untranslated regions and coding regions of mRNA to regulate ribosome recruitment and transit. Recently it has also been demonstrated that trans‐acting ribosomal proteins direct the translation of specific mRNAs. Importantly, it has been shown that subsets of RBPs often work in concert, forming distinct regulatory complexes upon different cellular perturbation, creating an RBP combinatorial code, which through the translation of specific subsets of mRNAs, dictate cell fate. With the development of new methodologies, a plethora of novel RNA binding proteins have recently been identified, although the function of many of these proteins within mRNA translation is unknown. In this review we will discuss these methodologies and their shortcomings when applied to the study of translation, which need to be addressed to enable a better understanding of trans‐acting translational regulatory proteins. Moreover, we discuss the protein domains that are responsible for RNA binding as well as the RNA motifs to which they bind, and the role of trans‐acting ribosomal proteins in directing the translation of specific mRNAs. 1.. RNA Interactions with Proteins and Other Molecules > RNA–Protein Complexes; 2.. Translation > Translation Regulation; 3.. Translation > Translation Mechanisms; John Wiley & Sons, Inc. 2018-01-17 2018 /pmc/articles/PMC5947564/ /pubmed/29341429 http://dx.doi.org/10.1002/wrna.1465 Text en © 2018 Medical Research Council and University of Cambridge. WIREs RNA published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Advanced Reviews
Harvey, Robert F.
Smith, Tom S.
Mulroney, Thomas
Queiroz, Rayner M. L.
Pizzinga, Mariavittoria
Dezi, Veronica
Villenueva, Eneko
Ramakrishna, Manasa
Lilley, Kathryn S.
Willis, Anne E.
Trans‐acting translational regulatory RNA binding proteins
title Trans‐acting translational regulatory RNA binding proteins
title_full Trans‐acting translational regulatory RNA binding proteins
title_fullStr Trans‐acting translational regulatory RNA binding proteins
title_full_unstemmed Trans‐acting translational regulatory RNA binding proteins
title_short Trans‐acting translational regulatory RNA binding proteins
title_sort trans‐acting translational regulatory rna binding proteins
topic Advanced Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947564/
https://www.ncbi.nlm.nih.gov/pubmed/29341429
http://dx.doi.org/10.1002/wrna.1465
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