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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...

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Autores principales: Gutierrez, J Ignacio, Brittingham, Gregory P, Karadeniz, Yonca, Tran, Kathleen D, Dutta, Arnob, Holehouse, Alex S, Peterson, Craig L, Holt, Liam J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
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.
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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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