4.7 Article

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

Journal

METHODS
Volume 193, Issue -, Pages 62-67

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2020.10.009

Keywords

Stress adaptation; Single-molecule microscopy; Transcription factors; Energy sources; Growth

Funding

  1. Royal Society Newton International Fellowship Alumni [AL\191025]
  2. Knut and Alice Wallenberg Foundation [KAW 2017-0091, KAW 2015.0272]
  3. Swedish Research Council [2019-03937]
  4. Biotechnology and Biological Sciences Research Council [BB/P000746/1]
  5. Newcastle University through the Newcastle Academic Track fellowship
  6. [289995]

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Research has found that different environmental signals result in unique single-molecule fluorescence patterns of the Mig1 transcription factor in the nucleus of budding yeast, acting as a 'barcode' of gene regulatory state that correlates with cell growth characteristics and other biological functions.
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 cer-evisiae. 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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