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SWI/SNF senses carbon starvation with a pH-sensitive low-complexity sequence
It is increasingly appreciated that intracellular pH changes are important biological signals. This motivates the elucidation of molecular mechanisms of pH sensing. We determined that a nucleocytoplasmic pH oscillation was required for the transcriptional response to carbon starvation in Saccharomyc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890752/ https://www.ncbi.nlm.nih.gov/pubmed/35129437 http://dx.doi.org/10.7554/eLife.70344 |
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author | Gutierrez, J Ignacio Brittingham, Gregory P Karadeniz, Yonca Tran, Kathleen D Dutta, Arnob Holehouse, Alex S Peterson, Craig L Holt, Liam J |
author_facet | Gutierrez, J Ignacio Brittingham, Gregory P Karadeniz, Yonca Tran, Kathleen D Dutta, Arnob Holehouse, Alex S Peterson, Craig L Holt, Liam J |
author_sort | Gutierrez, J Ignacio |
collection | PubMed |
description | It is increasingly appreciated that intracellular pH changes are important biological signals. This motivates the elucidation of molecular mechanisms of pH sensing. We determined that a nucleocytoplasmic pH oscillation was required for the transcriptional response to carbon starvation in Saccharomyces cerevisiae. The SWI/SNF chromatin remodeling complex is a key mediator of this transcriptional response. A glutamine-rich low-complexity domain (QLC) in the SNF5 subunit of this complex, and histidines within this sequence, was required for efficient transcriptional reprogramming. Furthermore, the SNF5 QLC mediated pH-dependent recruitment of SWI/SNF to an acidic transcription factor in a reconstituted nucleosome remodeling assay. Simulations showed that protonation of histidines within the SNF5 QLC leads to conformational expansion, providing a potential biophysical mechanism for regulation of these interactions. Together, our results indicate that pH changes are a second messenger for transcriptional reprogramming during carbon starvation and that the SNF5 QLC acts as a pH sensor. |
format | Online Article Text |
id | pubmed-8890752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88907522022-03-03 SWI/SNF senses carbon starvation with a pH-sensitive low-complexity sequence Gutierrez, J Ignacio Brittingham, Gregory P Karadeniz, Yonca Tran, Kathleen D Dutta, Arnob Holehouse, Alex S Peterson, Craig L Holt, Liam J eLife Biochemistry and Chemical Biology It is increasingly appreciated that intracellular pH changes are important biological signals. This motivates the elucidation of molecular mechanisms of pH sensing. We determined that a nucleocytoplasmic pH oscillation was required for the transcriptional response to carbon starvation in Saccharomyces cerevisiae. The SWI/SNF chromatin remodeling complex is a key mediator of this transcriptional response. A glutamine-rich low-complexity domain (QLC) in the SNF5 subunit of this complex, and histidines within this sequence, was required for efficient transcriptional reprogramming. Furthermore, the SNF5 QLC mediated pH-dependent recruitment of SWI/SNF to an acidic transcription factor in a reconstituted nucleosome remodeling assay. Simulations showed that protonation of histidines within the SNF5 QLC leads to conformational expansion, providing a potential biophysical mechanism for regulation of these interactions. Together, our results indicate that pH changes are a second messenger for transcriptional reprogramming during carbon starvation and that the SNF5 QLC acts as a pH sensor. eLife Sciences Publications, Ltd 2022-02-07 /pmc/articles/PMC8890752/ /pubmed/35129437 http://dx.doi.org/10.7554/eLife.70344 Text en © 2022, Gutierrez et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Gutierrez, J Ignacio Brittingham, Gregory P Karadeniz, Yonca Tran, Kathleen D Dutta, Arnob Holehouse, Alex S Peterson, Craig L Holt, Liam J SWI/SNF senses carbon starvation with a pH-sensitive low-complexity sequence |
title | SWI/SNF senses carbon starvation with a pH-sensitive low-complexity sequence |
title_full | SWI/SNF senses carbon starvation with a pH-sensitive low-complexity sequence |
title_fullStr | SWI/SNF senses carbon starvation with a pH-sensitive low-complexity sequence |
title_full_unstemmed | SWI/SNF senses carbon starvation with a pH-sensitive low-complexity sequence |
title_short | SWI/SNF senses carbon starvation with a pH-sensitive low-complexity sequence |
title_sort | swi/snf senses carbon starvation with a ph-sensitive low-complexity sequence |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890752/ https://www.ncbi.nlm.nih.gov/pubmed/35129437 http://dx.doi.org/10.7554/eLife.70344 |
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