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Nucleosome Remodeling at the Yeast PHO8 and PHO84 Promoters without the Putatively Essential SWI/SNF Remodeler

Chromatin remodeling by ATP-dependent remodeling enzymes is crucial for all genomic processes, like transcription or replication. Eukaryotes harbor many remodeler types, and it is unclear why a given chromatin transition requires more or less stringently one or several remodelers. As a classical exa...

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Autores principales: Lieleg, Corinna, Novacic, Ana, Musladin, Sanja, Schmid, Andrea, Akpinar, Gözde Güçlüler, Barbaric, Slobodan, Korber, Philipp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003099/
https://www.ncbi.nlm.nih.gov/pubmed/36902382
http://dx.doi.org/10.3390/ijms24054949
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author Lieleg, Corinna
Novacic, Ana
Musladin, Sanja
Schmid, Andrea
Akpinar, Gözde Güçlüler
Barbaric, Slobodan
Korber, Philipp
author_facet Lieleg, Corinna
Novacic, Ana
Musladin, Sanja
Schmid, Andrea
Akpinar, Gözde Güçlüler
Barbaric, Slobodan
Korber, Philipp
author_sort Lieleg, Corinna
collection PubMed
description Chromatin remodeling by ATP-dependent remodeling enzymes is crucial for all genomic processes, like transcription or replication. Eukaryotes harbor many remodeler types, and it is unclear why a given chromatin transition requires more or less stringently one or several remodelers. As a classical example, removal of budding yeast PHO8 and PHO84 promoter nucleosomes upon physiological gene induction by phosphate starvation essentially requires the SWI/SNF remodeling complex. This dependency on SWI/SNF may indicate specificity in remodeler recruitment, in recognition of nucleosomes as remodeling substrate or in remodeling outcome. By in vivo chromatin analyses of wild type and mutant yeast under various PHO regulon induction conditions, we found that overexpression of the remodeler-recruiting transactivator Pho4 allowed removal of PHO8 promoter nucleosomes without SWI/SNF. For PHO84 promoter nucleosome removal in the absence of SWI/SNF, an intranucleosomal Pho4 site, which likely altered the remodeling outcome via factor binding competition, was required in addition to such overexpression. Therefore, an essential remodeler requirement under physiological conditions need not reflect substrate specificity, but may reflect specific recruitment and/or remodeling outcomes.
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spelling pubmed-100030992023-03-11 Nucleosome Remodeling at the Yeast PHO8 and PHO84 Promoters without the Putatively Essential SWI/SNF Remodeler Lieleg, Corinna Novacic, Ana Musladin, Sanja Schmid, Andrea Akpinar, Gözde Güçlüler Barbaric, Slobodan Korber, Philipp Int J Mol Sci Article Chromatin remodeling by ATP-dependent remodeling enzymes is crucial for all genomic processes, like transcription or replication. Eukaryotes harbor many remodeler types, and it is unclear why a given chromatin transition requires more or less stringently one or several remodelers. As a classical example, removal of budding yeast PHO8 and PHO84 promoter nucleosomes upon physiological gene induction by phosphate starvation essentially requires the SWI/SNF remodeling complex. This dependency on SWI/SNF may indicate specificity in remodeler recruitment, in recognition of nucleosomes as remodeling substrate or in remodeling outcome. By in vivo chromatin analyses of wild type and mutant yeast under various PHO regulon induction conditions, we found that overexpression of the remodeler-recruiting transactivator Pho4 allowed removal of PHO8 promoter nucleosomes without SWI/SNF. For PHO84 promoter nucleosome removal in the absence of SWI/SNF, an intranucleosomal Pho4 site, which likely altered the remodeling outcome via factor binding competition, was required in addition to such overexpression. Therefore, an essential remodeler requirement under physiological conditions need not reflect substrate specificity, but may reflect specific recruitment and/or remodeling outcomes. MDPI 2023-03-03 /pmc/articles/PMC10003099/ /pubmed/36902382 http://dx.doi.org/10.3390/ijms24054949 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lieleg, Corinna
Novacic, Ana
Musladin, Sanja
Schmid, Andrea
Akpinar, Gözde Güçlüler
Barbaric, Slobodan
Korber, Philipp
Nucleosome Remodeling at the Yeast PHO8 and PHO84 Promoters without the Putatively Essential SWI/SNF Remodeler
title Nucleosome Remodeling at the Yeast PHO8 and PHO84 Promoters without the Putatively Essential SWI/SNF Remodeler
title_full Nucleosome Remodeling at the Yeast PHO8 and PHO84 Promoters without the Putatively Essential SWI/SNF Remodeler
title_fullStr Nucleosome Remodeling at the Yeast PHO8 and PHO84 Promoters without the Putatively Essential SWI/SNF Remodeler
title_full_unstemmed Nucleosome Remodeling at the Yeast PHO8 and PHO84 Promoters without the Putatively Essential SWI/SNF Remodeler
title_short Nucleosome Remodeling at the Yeast PHO8 and PHO84 Promoters without the Putatively Essential SWI/SNF Remodeler
title_sort nucleosome remodeling at the yeast pho8 and pho84 promoters without the putatively essential swi/snf remodeler
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003099/
https://www.ncbi.nlm.nih.gov/pubmed/36902382
http://dx.doi.org/10.3390/ijms24054949
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