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Ribosome heterogeneity and specialization in development

Regulation of protein synthesis is a vital step in controlling gene expression, especially during development. Over the last 10 years, it has become clear that rather than being homogeneous machines responsible for mRNA translation, ribosomes are highly heterogeneous and can play an active part in t...

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Autores principales: Norris, Karl, Hopes, Tayah, Aspden, Julie Louise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647923/
https://www.ncbi.nlm.nih.gov/pubmed/33565275
http://dx.doi.org/10.1002/wrna.1644
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author Norris, Karl
Hopes, Tayah
Aspden, Julie Louise
author_facet Norris, Karl
Hopes, Tayah
Aspden, Julie Louise
author_sort Norris, Karl
collection PubMed
description Regulation of protein synthesis is a vital step in controlling gene expression, especially during development. Over the last 10 years, it has become clear that rather than being homogeneous machines responsible for mRNA translation, ribosomes are highly heterogeneous and can play an active part in translational regulation. These “specialized ribosomes” comprise of specific protein and/or rRNA components, which are required for the translation of particular mRNAs. However, while there is extensive evidence for ribosome heterogeneity, support for specialized functions is limited. Recent work in a variety of developmental model organisms has shed some light on the biological relevance of ribosome heterogeneity. Tissue‐specific expression of ribosomal components along with phenotypic analysis of ribosomal gene mutations indicate that ribosome heterogeneity and potentially specialization are common in key development processes like embryogenesis, spermatogenesis, oogenesis, body patterning, and neurogenesis. Several examples of ribosome specialization have now been proposed but strong links between ribosome heterogeneity, translation of specific mRNAs by defined mechanisms, and role of these translation events remain elusive. Furthermore, several studies have indicated that heterogeneous ribosome populations are a product of tissue‐specific expression rather than specialized function and that ribosomal protein phenotypes are the result of extra‐ribosomal function or overall reduced ribosome levels. Many important questions still need to be addressed in order to determine the functional importance of ribosome heterogeneity to development and disease, which is likely to vary across systems. It will be essential to dissect these issues to fully understand diseases caused by disruptions to ribosomal composition, such as ribosomopathies. This article is categorized under: Translation > Translation Regulation. Translation > Ribosome Structure/Function. RNA in Disease and Development > RNA in Development.
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spelling pubmed-86479232021-12-20 Ribosome heterogeneity and specialization in development Norris, Karl Hopes, Tayah Aspden, Julie Louise Wiley Interdiscip Rev RNA Advanced Reviews Regulation of protein synthesis is a vital step in controlling gene expression, especially during development. Over the last 10 years, it has become clear that rather than being homogeneous machines responsible for mRNA translation, ribosomes are highly heterogeneous and can play an active part in translational regulation. These “specialized ribosomes” comprise of specific protein and/or rRNA components, which are required for the translation of particular mRNAs. However, while there is extensive evidence for ribosome heterogeneity, support for specialized functions is limited. Recent work in a variety of developmental model organisms has shed some light on the biological relevance of ribosome heterogeneity. Tissue‐specific expression of ribosomal components along with phenotypic analysis of ribosomal gene mutations indicate that ribosome heterogeneity and potentially specialization are common in key development processes like embryogenesis, spermatogenesis, oogenesis, body patterning, and neurogenesis. Several examples of ribosome specialization have now been proposed but strong links between ribosome heterogeneity, translation of specific mRNAs by defined mechanisms, and role of these translation events remain elusive. Furthermore, several studies have indicated that heterogeneous ribosome populations are a product of tissue‐specific expression rather than specialized function and that ribosomal protein phenotypes are the result of extra‐ribosomal function or overall reduced ribosome levels. Many important questions still need to be addressed in order to determine the functional importance of ribosome heterogeneity to development and disease, which is likely to vary across systems. It will be essential to dissect these issues to fully understand diseases caused by disruptions to ribosomal composition, such as ribosomopathies. This article is categorized under: Translation > Translation Regulation. Translation > Ribosome Structure/Function. RNA in Disease and Development > RNA in Development. John Wiley & Sons, Inc. 2021-02-09 2021 /pmc/articles/PMC8647923/ /pubmed/33565275 http://dx.doi.org/10.1002/wrna.1644 Text en © 2021 The Authors. WIREs RNA published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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
Norris, Karl
Hopes, Tayah
Aspden, Julie Louise
Ribosome heterogeneity and specialization in development
title Ribosome heterogeneity and specialization in development
title_full Ribosome heterogeneity and specialization in development
title_fullStr Ribosome heterogeneity and specialization in development
title_full_unstemmed Ribosome heterogeneity and specialization in development
title_short Ribosome heterogeneity and specialization in development
title_sort ribosome heterogeneity and specialization in development
topic Advanced Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647923/
https://www.ncbi.nlm.nih.gov/pubmed/33565275
http://dx.doi.org/10.1002/wrna.1644
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