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Regulation of ribosomal protein genes: An ordered anarchy

Ribosomal protein genes are among the most highly expressed genes in most cell types. Their products are generally essential for ribosome synthesis, which is the cornerstone for cell growth and proliferation. Many cellular resources are dedicated to producing ribosomal proteins and thus this process...

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Autores principales: Petibon, Cyrielle, Malik Ghulam, Mustafa, Catala, Mathieu, Abou Elela, Sherif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047918/
https://www.ncbi.nlm.nih.gov/pubmed/33038057
http://dx.doi.org/10.1002/wrna.1632
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author Petibon, Cyrielle
Malik Ghulam, Mustafa
Catala, Mathieu
Abou Elela, Sherif
author_facet Petibon, Cyrielle
Malik Ghulam, Mustafa
Catala, Mathieu
Abou Elela, Sherif
author_sort Petibon, Cyrielle
collection PubMed
description Ribosomal protein genes are among the most highly expressed genes in most cell types. Their products are generally essential for ribosome synthesis, which is the cornerstone for cell growth and proliferation. Many cellular resources are dedicated to producing ribosomal proteins and thus this process needs to be regulated in ways that carefully balance the supply of nascent ribosomal proteins with the demand for new ribosomes. Ribosomal protein genes have classically been viewed as a uniform interconnected regulon regulated in eukaryotic cells by target of rapamycin and protein kinase A pathway in response to changes in growth conditions and/or cellular status. However, recent literature depicts a more complex picture in which the amount of ribosomal proteins produced varies between genes in response to two overlapping regulatory circuits. The first includes the classical general ribosome‐producing program and the second is a gene‐specific feature responsible for fine‐tuning the amount of ribosomal proteins produced from each individual ribosomal gene. Unlike the general pathway that is mainly controlled at the level of transcription and translation, this specific regulation of ribosomal protein genes is largely achieved through changes in pre‐mRNA splicing efficiency and mRNA stability. By combining general and specific regulation, the cell can coordinate ribosome production, while allowing functional specialization and diversity. Here we review the many ways ribosomal protein genes are regulated, with special focus on the emerging role of posttranscriptional regulatory events in fine‐tuning the expression of ribosomal protein genes and its role in controlling the potential variation in ribosome functions. This article is categorized under: Translation > Ribosome Biogenesis. Translation > Ribosome Structure/Function. Translation > Translation Regulation.
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spelling pubmed-80479182021-04-16 Regulation of ribosomal protein genes: An ordered anarchy Petibon, Cyrielle Malik Ghulam, Mustafa Catala, Mathieu Abou Elela, Sherif Wiley Interdiscip Rev RNA Advanced Reviews Ribosomal protein genes are among the most highly expressed genes in most cell types. Their products are generally essential for ribosome synthesis, which is the cornerstone for cell growth and proliferation. Many cellular resources are dedicated to producing ribosomal proteins and thus this process needs to be regulated in ways that carefully balance the supply of nascent ribosomal proteins with the demand for new ribosomes. Ribosomal protein genes have classically been viewed as a uniform interconnected regulon regulated in eukaryotic cells by target of rapamycin and protein kinase A pathway in response to changes in growth conditions and/or cellular status. However, recent literature depicts a more complex picture in which the amount of ribosomal proteins produced varies between genes in response to two overlapping regulatory circuits. The first includes the classical general ribosome‐producing program and the second is a gene‐specific feature responsible for fine‐tuning the amount of ribosomal proteins produced from each individual ribosomal gene. Unlike the general pathway that is mainly controlled at the level of transcription and translation, this specific regulation of ribosomal protein genes is largely achieved through changes in pre‐mRNA splicing efficiency and mRNA stability. By combining general and specific regulation, the cell can coordinate ribosome production, while allowing functional specialization and diversity. Here we review the many ways ribosomal protein genes are regulated, with special focus on the emerging role of posttranscriptional regulatory events in fine‐tuning the expression of ribosomal protein genes and its role in controlling the potential variation in ribosome functions. This article is categorized under: Translation > Ribosome Biogenesis. Translation > Ribosome Structure/Function. Translation > Translation Regulation. John Wiley & Sons, Inc. 2020-10-10 2021 /pmc/articles/PMC8047918/ /pubmed/33038057 http://dx.doi.org/10.1002/wrna.1632 Text en © 2020 The Authors. WIREs RNA published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Advanced Reviews
Petibon, Cyrielle
Malik Ghulam, Mustafa
Catala, Mathieu
Abou Elela, Sherif
Regulation of ribosomal protein genes: An ordered anarchy
title Regulation of ribosomal protein genes: An ordered anarchy
title_full Regulation of ribosomal protein genes: An ordered anarchy
title_fullStr Regulation of ribosomal protein genes: An ordered anarchy
title_full_unstemmed Regulation of ribosomal protein genes: An ordered anarchy
title_short Regulation of ribosomal protein genes: An ordered anarchy
title_sort regulation of ribosomal protein genes: an ordered anarchy
topic Advanced Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047918/
https://www.ncbi.nlm.nih.gov/pubmed/33038057
http://dx.doi.org/10.1002/wrna.1632
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