Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo.

Nucleic Acids Res

Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USA.

Published: May 2017

AI Article Synopsis

  • The study investigates how changes in RNA Polymerase II (Pol II) activity influence gene expression in yeast, finding that both increased and decreased Pol II activity result in lower occupancy and reduced elongation rates in the cell.
  • The researchers note that measuring elongation rates in vivo can be complicated by transcription shutdown conditions and that gene expression defects vary depending on the specific promoter and template used.
  • The findings also reveal that while mRNA half-lives are extended in certain Pol II mutants, these changes do not align with predictions regarding the mutants' sensitivity to nucleotide depletion, suggesting a need for a nuanced understanding of transcription defects associated with altered Pol II activity.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416818PMC
http://dx.doi.org/10.1093/nar/gkx037DOI Listing

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