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A DEAD-box helicase drives the partitioning of a pro-differentiation NAB protein into nuclear foci
How cells regulate gene expression in a precise spatiotemporal manner during organismal development is a fundamental question in biology. Although the role of transcriptional condensates in gene regulation has been established, little is known about the function and regulation of these molecular ass...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584935/ https://www.ncbi.nlm.nih.gov/pubmed/37852948 http://dx.doi.org/10.1038/s41467-023-42345-9 |
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author | Doi, Akiko Suarez, Gianmarco D. Droste, Rita Horvitz, H. Robert |
author_facet | Doi, Akiko Suarez, Gianmarco D. Droste, Rita Horvitz, H. Robert |
author_sort | Doi, Akiko |
collection | PubMed |
description | How cells regulate gene expression in a precise spatiotemporal manner during organismal development is a fundamental question in biology. Although the role of transcriptional condensates in gene regulation has been established, little is known about the function and regulation of these molecular assemblies in the context of animal development and physiology. Here we show that the evolutionarily conserved DEAD-box helicase DDX-23 controls cell fate in Caenorhabditis elegans by binding to and facilitating the condensation of MAB-10, the C. elegans homolog of mammalian NGFI-A-binding (NAB) protein. MAB-10 is a transcriptional cofactor that functions with the early growth response (EGR) protein LIN-29 to regulate the transcription of genes required for exiting the cell cycle, terminal differentiation, and the larval-to-adult transition. We suggest that DEAD-box helicase proteins function more generally during animal development to control the condensation of NAB proteins important in cell identity and that this mechanism is evolutionarily conserved. In mammals, such a mechanism might underlie terminal cell differentiation and when dysregulated might promote cancerous growth. |
format | Online Article Text |
id | pubmed-10584935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105849352023-10-20 A DEAD-box helicase drives the partitioning of a pro-differentiation NAB protein into nuclear foci Doi, Akiko Suarez, Gianmarco D. Droste, Rita Horvitz, H. Robert Nat Commun Article How cells regulate gene expression in a precise spatiotemporal manner during organismal development is a fundamental question in biology. Although the role of transcriptional condensates in gene regulation has been established, little is known about the function and regulation of these molecular assemblies in the context of animal development and physiology. Here we show that the evolutionarily conserved DEAD-box helicase DDX-23 controls cell fate in Caenorhabditis elegans by binding to and facilitating the condensation of MAB-10, the C. elegans homolog of mammalian NGFI-A-binding (NAB) protein. MAB-10 is a transcriptional cofactor that functions with the early growth response (EGR) protein LIN-29 to regulate the transcription of genes required for exiting the cell cycle, terminal differentiation, and the larval-to-adult transition. We suggest that DEAD-box helicase proteins function more generally during animal development to control the condensation of NAB proteins important in cell identity and that this mechanism is evolutionarily conserved. In mammals, such a mechanism might underlie terminal cell differentiation and when dysregulated might promote cancerous growth. Nature Publishing Group UK 2023-10-18 /pmc/articles/PMC10584935/ /pubmed/37852948 http://dx.doi.org/10.1038/s41467-023-42345-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Doi, Akiko Suarez, Gianmarco D. Droste, Rita Horvitz, H. Robert A DEAD-box helicase drives the partitioning of a pro-differentiation NAB protein into nuclear foci |
title | A DEAD-box helicase drives the partitioning of a pro-differentiation NAB protein into nuclear foci |
title_full | A DEAD-box helicase drives the partitioning of a pro-differentiation NAB protein into nuclear foci |
title_fullStr | A DEAD-box helicase drives the partitioning of a pro-differentiation NAB protein into nuclear foci |
title_full_unstemmed | A DEAD-box helicase drives the partitioning of a pro-differentiation NAB protein into nuclear foci |
title_short | A DEAD-box helicase drives the partitioning of a pro-differentiation NAB protein into nuclear foci |
title_sort | dead-box helicase drives the partitioning of a pro-differentiation nab protein into nuclear foci |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584935/ https://www.ncbi.nlm.nih.gov/pubmed/37852948 http://dx.doi.org/10.1038/s41467-023-42345-9 |
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