NELF and DSIF cause promoter proximal pausing on the hsp70 promoter in Drosophila

  1. Chwen-Huey Wu1,
  2. Yuki Yamaguchi2,3,
  3. Lawrence R. Benjamin1,
  4. Maria Horvat-Gordon1,
  5. Jodi Washinsky1,
  6. Espen Enerly5,
  7. Jan Larsson6,
  8. Andrew Lambertsson5,
  9. Hiroshi Handa4, and
  10. David Gilmour1,7
  1. 1Center for Gene Regulation, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania 16802, USA; 2Faculty of Bioscience and Biotechnology, 3PRESTO-JST, and 4Frontier Collaborative Research Center, Tokyo Institute of Technology, Yokohama, Japan; 5Institute of Biology, Division of Cell and Molecular Biology, University of Oslo, Oslo, Norway; 6UCMP, Umeå University, SE-901 87 Umeå, Sweden

Abstract

NELF and DSIF collaborate to inhibit elongation by RNA polymerase IIa in extracts from human cells. A multifaceted approach was taken to investigate the potential role of these factors in promoter proximal pausing on the hsp70 gene in Drosophila. Immunodepletion of DSIF from a Drosophila nuclear extract reduced the level of polymerase that paused in the promoter proximal region of hsp70. Depletion of one NELF subunit in salivary glands using RNA interference also reduced the level of paused polymerase. In vivo protein–DNA cross-linking showed that NELF and DSIF associate with the promoter region before heat shock. Immunofluorescence analysis of polytene chromosomes corroborated the cross-linking result and showed that NELF, DSIF, and RNA polymerase IIa colocalize at the hsp70 genes, small heat shock genes, and many other chromosomal locations. Finally, following heat shock induction, DSIF and polymerase but not NELF were strongly recruited to chromosomal puffs harboring the hsp70 genes. We propose that NELF and DSIF cause polymerase to pause in the promoter proximal region of hsp70. The transcriptional activator, HSF, might cause NELF to dissociate from the elongation complex. DSIF continues to associate with the elongation complex and could serve a positive role in elongation.

Keywords

Footnotes

  • Corresponding author.

  • 7 E-MAIL dsg11{at}psu.edu; FAX (814) 863-7024.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.1091403.

    • Accepted April 2, 2003.
    • Received March 5, 2003.
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