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ReporterSeq reveals genome-wide dynamic modulators of the heat shock response across diverse stressors
Understanding cellular stress response pathways is challenging because of the complexity of regulatory mechanisms and response dynamics, which can vary with both time and the type of stress. We developed a reverse genetic method called ReporterSeq to comprehensively identify genes regulating a stres...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257254/ https://www.ncbi.nlm.nih.gov/pubmed/34223816 http://dx.doi.org/10.7554/eLife.57376 |
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author | Alford, Brian D Tassoni-Tsuchida, Eduardo Khan, Danish Work, Jeremy J Valiant, Gregory Brandman, Onn |
author_facet | Alford, Brian D Tassoni-Tsuchida, Eduardo Khan, Danish Work, Jeremy J Valiant, Gregory Brandman, Onn |
author_sort | Alford, Brian D |
collection | PubMed |
description | Understanding cellular stress response pathways is challenging because of the complexity of regulatory mechanisms and response dynamics, which can vary with both time and the type of stress. We developed a reverse genetic method called ReporterSeq to comprehensively identify genes regulating a stress-induced transcription factor under multiple conditions in a time-resolved manner. ReporterSeq links RNA-encoded barcode levels to pathway-specific output under genetic perturbations, allowing pooled pathway activity measurements via DNA sequencing alone and without cell enrichment or single-cell isolation. We used ReporterSeq to identify regulators of the heat shock response (HSR), a conserved, poorly understood transcriptional program that protects cells from proteotoxicity and is misregulated in disease. Genome-wide HSR regulation in budding yeast was assessed across 15 stress conditions, uncovering novel stress-specific, time-specific, and constitutive regulators. ReporterSeq can assess the genetic regulators of any transcriptional pathway with the scale of pooled genetic screens and the precision of pathway-specific readouts. |
format | Online Article Text |
id | pubmed-8257254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-82572542021-07-07 ReporterSeq reveals genome-wide dynamic modulators of the heat shock response across diverse stressors Alford, Brian D Tassoni-Tsuchida, Eduardo Khan, Danish Work, Jeremy J Valiant, Gregory Brandman, Onn eLife Cell Biology Understanding cellular stress response pathways is challenging because of the complexity of regulatory mechanisms and response dynamics, which can vary with both time and the type of stress. We developed a reverse genetic method called ReporterSeq to comprehensively identify genes regulating a stress-induced transcription factor under multiple conditions in a time-resolved manner. ReporterSeq links RNA-encoded barcode levels to pathway-specific output under genetic perturbations, allowing pooled pathway activity measurements via DNA sequencing alone and without cell enrichment or single-cell isolation. We used ReporterSeq to identify regulators of the heat shock response (HSR), a conserved, poorly understood transcriptional program that protects cells from proteotoxicity and is misregulated in disease. Genome-wide HSR regulation in budding yeast was assessed across 15 stress conditions, uncovering novel stress-specific, time-specific, and constitutive regulators. ReporterSeq can assess the genetic regulators of any transcriptional pathway with the scale of pooled genetic screens and the precision of pathway-specific readouts. eLife Sciences Publications, Ltd 2021-07-05 /pmc/articles/PMC8257254/ /pubmed/34223816 http://dx.doi.org/10.7554/eLife.57376 Text en © 2021, Alford 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 | Cell Biology Alford, Brian D Tassoni-Tsuchida, Eduardo Khan, Danish Work, Jeremy J Valiant, Gregory Brandman, Onn ReporterSeq reveals genome-wide dynamic modulators of the heat shock response across diverse stressors |
title | ReporterSeq reveals genome-wide dynamic modulators of the heat shock response across diverse stressors |
title_full | ReporterSeq reveals genome-wide dynamic modulators of the heat shock response across diverse stressors |
title_fullStr | ReporterSeq reveals genome-wide dynamic modulators of the heat shock response across diverse stressors |
title_full_unstemmed | ReporterSeq reveals genome-wide dynamic modulators of the heat shock response across diverse stressors |
title_short | ReporterSeq reveals genome-wide dynamic modulators of the heat shock response across diverse stressors |
title_sort | reporterseq reveals genome-wide dynamic modulators of the heat shock response across diverse stressors |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257254/ https://www.ncbi.nlm.nih.gov/pubmed/34223816 http://dx.doi.org/10.7554/eLife.57376 |
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