Cargando…

A transcriptional cofactor regulatory network for the C. elegans intestine

Chromatin modifiers and transcriptional cofactors (collectively referred to as CFs) work with DNA-binding transcription factors (TFs) to regulate gene expression. In multicellular eukaryotes, distinct tissues each execute their own gene expression program for accurate differentiation and subsequent...

Descripción completa

Detalles Bibliográficos
Autores principales: Horowitz, Brent B, Nanda, Shivani, Walhout, Albertha J M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320766/
https://www.ncbi.nlm.nih.gov/pubmed/37119809
http://dx.doi.org/10.1093/g3journal/jkad096
_version_ 1785068504779587584
author Horowitz, Brent B
Nanda, Shivani
Walhout, Albertha J M
author_facet Horowitz, Brent B
Nanda, Shivani
Walhout, Albertha J M
author_sort Horowitz, Brent B
collection PubMed
description Chromatin modifiers and transcriptional cofactors (collectively referred to as CFs) work with DNA-binding transcription factors (TFs) to regulate gene expression. In multicellular eukaryotes, distinct tissues each execute their own gene expression program for accurate differentiation and subsequent functionality. While the function of TFs in differential gene expression has been studied in detail in many systems, the contribution of CFs has remained less explored. Here, we uncovered the contributions of CFs to gene regulation in the Caenorhabditis elegans intestine. We first annotated 366 CFs encoded by the C. elegans genome and assembled a library of 335 RNAi clones. Using this library, we analyzed the effects of individually depleting these CFs on the expression of 19 fluorescent transcriptional reporters in the intestine and identified 216 regulatory interactions. We found that different CFs regulate different promoters, and that both essential and intestinally expressed CFs have the greatest effects on promoter activity. We did not find all members of CF complexes acting on the same set of reporters but instead found diversity in the promoter targets of each complex component. Finally, we found that previously identified activation mechanisms for the acdh-1 promoter use different CFs and TFs. Overall, we demonstrate that CFs function specifically rather than ubiquitously at intestinal promoters and provide an RNAi resource for reverse genetic screens.
format Online
Article
Text
id pubmed-10320766
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-103207662023-07-06 A transcriptional cofactor regulatory network for the C. elegans intestine Horowitz, Brent B Nanda, Shivani Walhout, Albertha J M G3 (Bethesda) Investigation Chromatin modifiers and transcriptional cofactors (collectively referred to as CFs) work with DNA-binding transcription factors (TFs) to regulate gene expression. In multicellular eukaryotes, distinct tissues each execute their own gene expression program for accurate differentiation and subsequent functionality. While the function of TFs in differential gene expression has been studied in detail in many systems, the contribution of CFs has remained less explored. Here, we uncovered the contributions of CFs to gene regulation in the Caenorhabditis elegans intestine. We first annotated 366 CFs encoded by the C. elegans genome and assembled a library of 335 RNAi clones. Using this library, we analyzed the effects of individually depleting these CFs on the expression of 19 fluorescent transcriptional reporters in the intestine and identified 216 regulatory interactions. We found that different CFs regulate different promoters, and that both essential and intestinally expressed CFs have the greatest effects on promoter activity. We did not find all members of CF complexes acting on the same set of reporters but instead found diversity in the promoter targets of each complex component. Finally, we found that previously identified activation mechanisms for the acdh-1 promoter use different CFs and TFs. Overall, we demonstrate that CFs function specifically rather than ubiquitously at intestinal promoters and provide an RNAi resource for reverse genetic screens. Oxford University Press 2023-04-29 /pmc/articles/PMC10320766/ /pubmed/37119809 http://dx.doi.org/10.1093/g3journal/jkad096 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of The Genetics Society of America. 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/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Horowitz, Brent B
Nanda, Shivani
Walhout, Albertha J M
A transcriptional cofactor regulatory network for the C. elegans intestine
title A transcriptional cofactor regulatory network for the C. elegans intestine
title_full A transcriptional cofactor regulatory network for the C. elegans intestine
title_fullStr A transcriptional cofactor regulatory network for the C. elegans intestine
title_full_unstemmed A transcriptional cofactor regulatory network for the C. elegans intestine
title_short A transcriptional cofactor regulatory network for the C. elegans intestine
title_sort transcriptional cofactor regulatory network for the c. elegans intestine
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320766/
https://www.ncbi.nlm.nih.gov/pubmed/37119809
http://dx.doi.org/10.1093/g3journal/jkad096
work_keys_str_mv AT horowitzbrentb atranscriptionalcofactorregulatorynetworkforthecelegansintestine
AT nandashivani atranscriptionalcofactorregulatorynetworkforthecelegansintestine
AT walhoutalberthajm atranscriptionalcofactorregulatorynetworkforthecelegansintestine
AT horowitzbrentb transcriptionalcofactorregulatorynetworkforthecelegansintestine
AT nandashivani transcriptionalcofactorregulatorynetworkforthecelegansintestine
AT walhoutalberthajm transcriptionalcofactorregulatorynetworkforthecelegansintestine