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The microprotein Nrs1 rewires the G1/S transcriptional machinery during nitrogen limitation in budding yeast

Commitment to cell division at the end of G1 phase, termed Start in the budding yeast Saccharomyces cerevisiae, is strongly influenced by nutrient availability. To identify new dominant activators of Start that might operate under different nutrient conditions, we screened a genome-wide ORF overexpr...

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Autores principales: Tollis, Sylvain, Singh, Jaspal, Palou, Roger, Thattikota, Yogitha, Ghazal, Ghada, Coulombe-Huntington, Jasmin, Tang, Xiaojing, Moore, Susan, Blake, Deborah, Bonneil, Eric, Royer, Catherine A., Thibault, Pierre, Tyers, Mike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8893695/
https://www.ncbi.nlm.nih.gov/pubmed/35239649
http://dx.doi.org/10.1371/journal.pbio.3001548
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author Tollis, Sylvain
Singh, Jaspal
Palou, Roger
Thattikota, Yogitha
Ghazal, Ghada
Coulombe-Huntington, Jasmin
Tang, Xiaojing
Moore, Susan
Blake, Deborah
Bonneil, Eric
Royer, Catherine A.
Thibault, Pierre
Tyers, Mike
author_facet Tollis, Sylvain
Singh, Jaspal
Palou, Roger
Thattikota, Yogitha
Ghazal, Ghada
Coulombe-Huntington, Jasmin
Tang, Xiaojing
Moore, Susan
Blake, Deborah
Bonneil, Eric
Royer, Catherine A.
Thibault, Pierre
Tyers, Mike
author_sort Tollis, Sylvain
collection PubMed
description Commitment to cell division at the end of G1 phase, termed Start in the budding yeast Saccharomyces cerevisiae, is strongly influenced by nutrient availability. To identify new dominant activators of Start that might operate under different nutrient conditions, we screened a genome-wide ORF overexpression library for genes that bypass a Start arrest caused by absence of the G1 cyclin Cln3 and the transcriptional activator Bck2. We recovered a hypothetical gene YLR053c, renamed NRS1 for Nitrogen-Responsive Start regulator 1, which encodes a poorly characterized 108 amino acid microprotein. Endogenous Nrs1 was nuclear-localized, restricted to poor nitrogen conditions, induced upon TORC1 inhibition, and cell cycle-regulated with a peak at Start. NRS1 interacted genetically with SWI4 and SWI6, which encode subunits of the main G1/S transcription factor complex SBF. Correspondingly, Nrs1 physically interacted with Swi4 and Swi6 and was localized to G1/S promoter DNA. Nrs1 exhibited inherent transactivation activity, and fusion of Nrs1 to the SBF inhibitor Whi5 was sufficient to suppress other Start defects. Nrs1 appears to be a recently evolved microprotein that rewires the G1/S transcriptional machinery under poor nitrogen conditions.
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spelling pubmed-88936952022-03-04 The microprotein Nrs1 rewires the G1/S transcriptional machinery during nitrogen limitation in budding yeast Tollis, Sylvain Singh, Jaspal Palou, Roger Thattikota, Yogitha Ghazal, Ghada Coulombe-Huntington, Jasmin Tang, Xiaojing Moore, Susan Blake, Deborah Bonneil, Eric Royer, Catherine A. Thibault, Pierre Tyers, Mike PLoS Biol Research Article Commitment to cell division at the end of G1 phase, termed Start in the budding yeast Saccharomyces cerevisiae, is strongly influenced by nutrient availability. To identify new dominant activators of Start that might operate under different nutrient conditions, we screened a genome-wide ORF overexpression library for genes that bypass a Start arrest caused by absence of the G1 cyclin Cln3 and the transcriptional activator Bck2. We recovered a hypothetical gene YLR053c, renamed NRS1 for Nitrogen-Responsive Start regulator 1, which encodes a poorly characterized 108 amino acid microprotein. Endogenous Nrs1 was nuclear-localized, restricted to poor nitrogen conditions, induced upon TORC1 inhibition, and cell cycle-regulated with a peak at Start. NRS1 interacted genetically with SWI4 and SWI6, which encode subunits of the main G1/S transcription factor complex SBF. Correspondingly, Nrs1 physically interacted with Swi4 and Swi6 and was localized to G1/S promoter DNA. Nrs1 exhibited inherent transactivation activity, and fusion of Nrs1 to the SBF inhibitor Whi5 was sufficient to suppress other Start defects. Nrs1 appears to be a recently evolved microprotein that rewires the G1/S transcriptional machinery under poor nitrogen conditions. Public Library of Science 2022-03-03 /pmc/articles/PMC8893695/ /pubmed/35239649 http://dx.doi.org/10.1371/journal.pbio.3001548 Text en © 2022 Tollis et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Tollis, Sylvain
Singh, Jaspal
Palou, Roger
Thattikota, Yogitha
Ghazal, Ghada
Coulombe-Huntington, Jasmin
Tang, Xiaojing
Moore, Susan
Blake, Deborah
Bonneil, Eric
Royer, Catherine A.
Thibault, Pierre
Tyers, Mike
The microprotein Nrs1 rewires the G1/S transcriptional machinery during nitrogen limitation in budding yeast
title The microprotein Nrs1 rewires the G1/S transcriptional machinery during nitrogen limitation in budding yeast
title_full The microprotein Nrs1 rewires the G1/S transcriptional machinery during nitrogen limitation in budding yeast
title_fullStr The microprotein Nrs1 rewires the G1/S transcriptional machinery during nitrogen limitation in budding yeast
title_full_unstemmed The microprotein Nrs1 rewires the G1/S transcriptional machinery during nitrogen limitation in budding yeast
title_short The microprotein Nrs1 rewires the G1/S transcriptional machinery during nitrogen limitation in budding yeast
title_sort microprotein nrs1 rewires the g1/s transcriptional machinery during nitrogen limitation in budding yeast
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8893695/
https://www.ncbi.nlm.nih.gov/pubmed/35239649
http://dx.doi.org/10.1371/journal.pbio.3001548
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