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Transcriptional lockdown during acute proteotoxic stress

Cells experiencing proteotoxic stress downregulate the expression of thousands of active genes and upregulate a few stress-response genes. The strategy of downregulating gene expression has conceptual parallels with general lockdown in the global response to the coronavirus disease 2019 (COVID-19) p...

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Detalles Bibliográficos
Autor principal: Sawarkar, Ritwick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9041648/
https://www.ncbi.nlm.nih.gov/pubmed/35487807
http://dx.doi.org/10.1016/j.tibs.2022.03.020
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author Sawarkar, Ritwick
author_facet Sawarkar, Ritwick
author_sort Sawarkar, Ritwick
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description Cells experiencing proteotoxic stress downregulate the expression of thousands of active genes and upregulate a few stress-response genes. The strategy of downregulating gene expression has conceptual parallels with general lockdown in the global response to the coronavirus disease 2019 (COVID-19) pandemic. The mechanistic details of global transcriptional downregulation of genes, termed stress-induced transcriptional attenuation (SITA), are only beginning to emerge. The reduction in RNA and protein production during stress may spare proteostasis capacity, allowing cells to divert resources to control stress-induced damage. Given the relevance of translational downregulation in a broad variety of diseases, the role of SITA in diseases caused by proteotoxicity should be investigated in future, paving the way for potential novel therapeutics.
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spelling pubmed-90416482022-04-27 Transcriptional lockdown during acute proteotoxic stress Sawarkar, Ritwick Trends Biochem Sci Review Cells experiencing proteotoxic stress downregulate the expression of thousands of active genes and upregulate a few stress-response genes. The strategy of downregulating gene expression has conceptual parallels with general lockdown in the global response to the coronavirus disease 2019 (COVID-19) pandemic. The mechanistic details of global transcriptional downregulation of genes, termed stress-induced transcriptional attenuation (SITA), are only beginning to emerge. The reduction in RNA and protein production during stress may spare proteostasis capacity, allowing cells to divert resources to control stress-induced damage. Given the relevance of translational downregulation in a broad variety of diseases, the role of SITA in diseases caused by proteotoxicity should be investigated in future, paving the way for potential novel therapeutics. Elsevier Ltd. 2022-08 2022-04-26 /pmc/articles/PMC9041648/ /pubmed/35487807 http://dx.doi.org/10.1016/j.tibs.2022.03.020 Text en © 2022 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review
Sawarkar, Ritwick
Transcriptional lockdown during acute proteotoxic stress
title Transcriptional lockdown during acute proteotoxic stress
title_full Transcriptional lockdown during acute proteotoxic stress
title_fullStr Transcriptional lockdown during acute proteotoxic stress
title_full_unstemmed Transcriptional lockdown during acute proteotoxic stress
title_short Transcriptional lockdown during acute proteotoxic stress
title_sort transcriptional lockdown during acute proteotoxic stress
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9041648/
https://www.ncbi.nlm.nih.gov/pubmed/35487807
http://dx.doi.org/10.1016/j.tibs.2022.03.020
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