Cargando…
Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo
Here we employ a set of RNA Polymerase II (Pol II) activity mutants to determine the consequences of increased or decreased Pol II catalysis on gene expression in Saccharomyces cerevisiae. We find that alteration of Pol II catalytic rate, either fast or slow, leads to decreased Pol II occupancy and...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416818/ https://www.ncbi.nlm.nih.gov/pubmed/28119420 http://dx.doi.org/10.1093/nar/gkx037 |
_version_ | 1783233826253701120 |
---|---|
author | Malik, Indranil Qiu, Chenxi Snavely, Thomas Kaplan, Craig D. |
author_facet | Malik, Indranil Qiu, Chenxi Snavely, Thomas Kaplan, Craig D. |
author_sort | Malik, Indranil |
collection | PubMed |
description | Here we employ a set of RNA Polymerase II (Pol II) activity mutants to determine the consequences of increased or decreased Pol II catalysis on gene expression in Saccharomyces cerevisiae. We find that alteration of Pol II catalytic rate, either fast or slow, leads to decreased Pol II occupancy and apparent reduction in elongation rate in vivo. However, we also find that determination of elongation rate in vivo by chromatin immunoprecipitation can be confounded by the kinetics and conditions of transcriptional shutoff in the assay. We identify promoter and template-specific effects on severity of gene expression defects for both fast and slow Pol II mutants. We show that mRNA half-lives for a reporter gene are increased in both fast and slow Pol II mutant strains and the magnitude of half-life changes correlate both with mutants’ growth and reporter expression defects. Finally, we tested a model that altered Pol II activity sensitizes cells to nucleotide depletion. In contrast to model predictions, mutated Pol II retains normal sensitivity to altered nucleotide levels. Our experiments establish a framework for understanding the diversity of transcription defects derived from altered Pol II activity mutants, essential for their use as probes of transcription mechanisms. |
format | Online Article Text |
id | pubmed-5416818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54168182017-05-05 Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo Malik, Indranil Qiu, Chenxi Snavely, Thomas Kaplan, Craig D. Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Here we employ a set of RNA Polymerase II (Pol II) activity mutants to determine the consequences of increased or decreased Pol II catalysis on gene expression in Saccharomyces cerevisiae. We find that alteration of Pol II catalytic rate, either fast or slow, leads to decreased Pol II occupancy and apparent reduction in elongation rate in vivo. However, we also find that determination of elongation rate in vivo by chromatin immunoprecipitation can be confounded by the kinetics and conditions of transcriptional shutoff in the assay. We identify promoter and template-specific effects on severity of gene expression defects for both fast and slow Pol II mutants. We show that mRNA half-lives for a reporter gene are increased in both fast and slow Pol II mutant strains and the magnitude of half-life changes correlate both with mutants’ growth and reporter expression defects. Finally, we tested a model that altered Pol II activity sensitizes cells to nucleotide depletion. In contrast to model predictions, mutated Pol II retains normal sensitivity to altered nucleotide levels. Our experiments establish a framework for understanding the diversity of transcription defects derived from altered Pol II activity mutants, essential for their use as probes of transcription mechanisms. Oxford University Press 2017-05-05 2017-01-24 /pmc/articles/PMC5416818/ /pubmed/28119420 http://dx.doi.org/10.1093/nar/gkx037 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Malik, Indranil Qiu, Chenxi Snavely, Thomas Kaplan, Craig D. Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo |
title | Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo |
title_full | Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo |
title_fullStr | Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo |
title_full_unstemmed | Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo |
title_short | Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo |
title_sort | wide-ranging and unexpected consequences of altered pol ii catalytic activity in vivo |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416818/ https://www.ncbi.nlm.nih.gov/pubmed/28119420 http://dx.doi.org/10.1093/nar/gkx037 |
work_keys_str_mv | AT malikindranil widerangingandunexpectedconsequencesofalteredpoliicatalyticactivityinvivo AT qiuchenxi widerangingandunexpectedconsequencesofalteredpoliicatalyticactivityinvivo AT snavelythomas widerangingandunexpectedconsequencesofalteredpoliicatalyticactivityinvivo AT kaplancraigd widerangingandunexpectedconsequencesofalteredpoliicatalyticactivityinvivo |