Transcription factors GAF and HSF act at distinct regulatory steps to modulate stress-induced gene activation

  1. John T. Lis1
  1. 1Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14835, USA;
  2. 2Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, Virginia 22908, USA
  1. Corresponding authors: johnlis{at}cornell.edu, mjg7y{at}virginia.edu
  • Present addresses: 3Department of Molecular and Cell Biology, University of California at Berkeley, Berkeley, CA 94720, USA; 4Department of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, USA.

Abstract

The coordinated regulation of gene expression at the transcriptional level is fundamental to development and homeostasis. Inducible systems are invaluable when studying transcription because the regulatory process can be triggered instantaneously, allowing the tracking of ordered mechanistic events. Here, we use precision run-on sequencing (PRO-seq) to examine the genome-wide heat shock (HS) response in Drosophila and the function of two key transcription factors on the immediate transcription activation or repression of all genes regulated by HS. We identify the primary HS response genes and the rate-limiting steps in the transcription cycle that GAGA-associated factor (GAF) and HS factor (HSF) regulate. We demonstrate that GAF acts upstream of promoter-proximally paused RNA polymerase II (Pol II) formation (likely at the step of chromatin opening) and that GAF-facilitated Pol II pausing is critical for HS activation. In contrast, HSF is dispensable for establishing or maintaining Pol II pausing but is critical for the release of paused Pol II into the gene body at a subset of highly activated genes. Additionally, HSF has no detectable role in the rapid HS repression of thousands of genes.

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Footnotes

  • Supplemental material is available for this article.

  • Article published online ahead of print. Article and publication date are online at http://www.genesdev.org/cgi/doi/10.1101/gad.284430.116.

  • Freely available online through the Genes & Development Open Access option.

  • Received May 24, 2016.
  • Accepted July 11, 2016.

This article, published in Genes & Development, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.

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