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dc.contributor.authorGutiérrez, J. Ignacio
dc.contributor.authorBrittingham, Gregory P.
dc.contributor.authorKaradeniz, Yonca
dc.contributor.authorTran, Kathleen D.
dc.contributor.authorDutta, Arnob
dc.contributor.authorHolehouse, Alex S.
dc.contributor.authorPeterson, Craig L.
dc.contributor.authorHolt, Liam J.
dc.date2022-08-11T08:08:26.000
dc.date.accessioned2022-08-23T15:55:15Z
dc.date.available2022-08-23T15:55:15Z
dc.date.issued2021-03-03
dc.date.submitted2021-03-18
dc.identifier.citation<p>bioRxiv 2021.03.03.433592; doi: https://doi.org/10.1101/2021.03.03.433592. <a href="https://doi.org/10.1101/2021.03.03.433592" target="_blank" title="view preprint on bioRxiv">Link to preprint on bioRxiv</a></p>
dc.identifier.doi10.1101/2021.03.03.433592
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29714
dc.description<p>This article is a preprint. Preprints are preliminary reports of work that have not been certified by peer review.</p>
dc.description.abstractIt 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 S. cerevisiae. The SWI/SNF chromatin remodeling complex is a key mediator of this transcriptional response. We found that a glutamine-rich low complexity sequence (QLC) in the SNF5 subunit of this complex, and histidines within this sequence, were required for efficient transcriptional reprogramming during carbon starvation. Furthermore, the SNF5 QLC mediated pH-dependent recruitment of SWI/SNF to a model promoter in vitro. Simulations showed that protonation of histidines within the SNF5 QLC lead to conformational expansion, providing a potential biophysical mechanism for regulation of these interactions. Together, our results indicate that that pH changes are a second messenger for transcriptional reprogramming during carbon starvation, and that the SNF5 QLC acts as a pH-sensor.
dc.language.isoen_US
dc.rightsThe copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectMolecular Biology
dc.subjectcarbon starvation
dc.subjectintracellular pH changes
dc.subjecthistidines
dc.subjectGenes and Chromosomes
dc.subjectBiochemistry
dc.subjectBiophysics
dc.subjectBiochemistry
dc.subjectBiophysics
dc.subjectFungi
dc.subjectMolecular Biology
dc.titleSWI/SNF senses carbon starvation with a pH-sensitive low complexity sequence [preprint]
dc.typePreprint
dc.source.journaltitlebioRxiv
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2950&amp;context=faculty_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1927
dc.identifier.contextkey22096968
refterms.dateFOA2022-08-23T15:55:16Z
html.description.abstract<p><p id="x-x-x-p-2">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 <em>S. cerevisiae</em>. The SWI/SNF chromatin remodeling complex is a key mediator of this transcriptional response. We found that a glutamine-rich low complexity sequence (QLC) in the <em>SNF5</em> subunit of this complex, and histidines within this sequence, were required for efficient transcriptional reprogramming during carbon starvation. Furthermore, the <em>SNF5</em> QLC mediated pH-dependent recruitment of SWI/SNF to a model promoter <em>in vitro.</em> Simulations showed that protonation of histidines within the <em>SNF5</em> QLC lead to conformational expansion, providing a potential biophysical mechanism for regulation of these interactions. Together, our results indicate that that pH changes are a second messenger for transcriptional reprogramming during carbon starvation, and that the <em>SNF5</em> QLC acts as a pH-sensor.</p>
dc.identifier.submissionpathfaculty_pubs/1927
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.contributor.departmentProgram in Molecular Medicine


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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license
Except where otherwise noted, this item's license is described as The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license