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Clearing the slate: RNA turnover to enable cell state switching?
The distribution of mRNA in tissue is determined by the balance between transcription and decay. Understanding the control of RNA decay during development has been somewhat neglected compared with transcriptional control. Here, we explore the potential for mRNA decay to trigger rapid cell state tran...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617622/ https://www.ncbi.nlm.nih.gov/pubmed/37831057 http://dx.doi.org/10.1242/dev.202084 |
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author | Westbrook, Elizabeth R. Ford, Hugh Z. Antolović, Vlatka Chubb, Jonathan R. |
author_facet | Westbrook, Elizabeth R. Ford, Hugh Z. Antolović, Vlatka Chubb, Jonathan R. |
author_sort | Westbrook, Elizabeth R. |
collection | PubMed |
description | The distribution of mRNA in tissue is determined by the balance between transcription and decay. Understanding the control of RNA decay during development has been somewhat neglected compared with transcriptional control. Here, we explore the potential for mRNA decay to trigger rapid cell state transitions during development, comparing a bistable switch model of cell state conversion with experimental evidence from different developmental systems. We also consider another potential role for large-scale RNA decay that has emerged from studies of stress-induced cell state transitions, in which removal of mRNA unblocks the translation machinery to prioritise the synthesis of proteins that establish the new cell state. |
format | Online Article Text |
id | pubmed-10617622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-106176222023-11-01 Clearing the slate: RNA turnover to enable cell state switching? Westbrook, Elizabeth R. Ford, Hugh Z. Antolović, Vlatka Chubb, Jonathan R. Development Spotlight The distribution of mRNA in tissue is determined by the balance between transcription and decay. Understanding the control of RNA decay during development has been somewhat neglected compared with transcriptional control. Here, we explore the potential for mRNA decay to trigger rapid cell state transitions during development, comparing a bistable switch model of cell state conversion with experimental evidence from different developmental systems. We also consider another potential role for large-scale RNA decay that has emerged from studies of stress-induced cell state transitions, in which removal of mRNA unblocks the translation machinery to prioritise the synthesis of proteins that establish the new cell state. The Company of Biologists Ltd 2023-10-12 /pmc/articles/PMC10617622/ /pubmed/37831057 http://dx.doi.org/10.1242/dev.202084 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Spotlight Westbrook, Elizabeth R. Ford, Hugh Z. Antolović, Vlatka Chubb, Jonathan R. Clearing the slate: RNA turnover to enable cell state switching? |
title | Clearing the slate: RNA turnover to enable cell state switching? |
title_full | Clearing the slate: RNA turnover to enable cell state switching? |
title_fullStr | Clearing the slate: RNA turnover to enable cell state switching? |
title_full_unstemmed | Clearing the slate: RNA turnover to enable cell state switching? |
title_short | Clearing the slate: RNA turnover to enable cell state switching? |
title_sort | clearing the slate: rna turnover to enable cell state switching? |
topic | Spotlight |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617622/ https://www.ncbi.nlm.nih.gov/pubmed/37831057 http://dx.doi.org/10.1242/dev.202084 |
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