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Correlative single-molecule fluorescence barcoding of gene regulation in Saccharomyces cerevisiae

Most cells adapt to their environment by switching combinations of genes on and off through a complex interplay of transcription factor proteins (TFs). The mechanisms by which TFs respond to signals, move into the nucleus and find specific binding sites in target genes is still largely unknown. Sing...

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Autores principales: Shashkova, Sviatlana, Nyström, Thomas, Leake, Mark C., Wollman, Adam J.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343463/
https://www.ncbi.nlm.nih.gov/pubmed/33086048
http://dx.doi.org/10.1016/j.ymeth.2020.10.009
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author Shashkova, Sviatlana
Nyström, Thomas
Leake, Mark C.
Wollman, Adam J.M.
author_facet Shashkova, Sviatlana
Nyström, Thomas
Leake, Mark C.
Wollman, Adam J.M.
author_sort Shashkova, Sviatlana
collection PubMed
description Most cells adapt to their environment by switching combinations of genes on and off through a complex interplay of transcription factor proteins (TFs). The mechanisms by which TFs respond to signals, move into the nucleus and find specific binding sites in target genes is still largely unknown. Single-molecule fluorescence microscopes, which can image single TFs in live cells, have begun to elucidate the problem. Here, we show that different environmental signals, in this case carbon sources, yield a unique single-molecule fluorescence pattern of foci of a key metabolic regulating transcription factor, Mig1, in the nucleus of the budding yeast, Saccharomyces cerevisiae. This pattern serves as a ‘barcode’ of the gene regulatory state of the cells which can be correlated with cell growth characteristics and other biological function.
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spelling pubmed-83434632021-09-01 Correlative single-molecule fluorescence barcoding of gene regulation in Saccharomyces cerevisiae Shashkova, Sviatlana Nyström, Thomas Leake, Mark C. Wollman, Adam J.M. Methods Article Most cells adapt to their environment by switching combinations of genes on and off through a complex interplay of transcription factor proteins (TFs). The mechanisms by which TFs respond to signals, move into the nucleus and find specific binding sites in target genes is still largely unknown. Single-molecule fluorescence microscopes, which can image single TFs in live cells, have begun to elucidate the problem. Here, we show that different environmental signals, in this case carbon sources, yield a unique single-molecule fluorescence pattern of foci of a key metabolic regulating transcription factor, Mig1, in the nucleus of the budding yeast, Saccharomyces cerevisiae. This pattern serves as a ‘barcode’ of the gene regulatory state of the cells which can be correlated with cell growth characteristics and other biological function. Academic Press 2021-09 /pmc/articles/PMC8343463/ /pubmed/33086048 http://dx.doi.org/10.1016/j.ymeth.2020.10.009 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shashkova, Sviatlana
Nyström, Thomas
Leake, Mark C.
Wollman, Adam J.M.
Correlative single-molecule fluorescence barcoding of gene regulation in Saccharomyces cerevisiae
title Correlative single-molecule fluorescence barcoding of gene regulation in Saccharomyces cerevisiae
title_full Correlative single-molecule fluorescence barcoding of gene regulation in Saccharomyces cerevisiae
title_fullStr Correlative single-molecule fluorescence barcoding of gene regulation in Saccharomyces cerevisiae
title_full_unstemmed Correlative single-molecule fluorescence barcoding of gene regulation in Saccharomyces cerevisiae
title_short Correlative single-molecule fluorescence barcoding of gene regulation in Saccharomyces cerevisiae
title_sort correlative single-molecule fluorescence barcoding of gene regulation in saccharomyces cerevisiae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343463/
https://www.ncbi.nlm.nih.gov/pubmed/33086048
http://dx.doi.org/10.1016/j.ymeth.2020.10.009
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