Identification of a Novel cis-Regulatory Element Involved in the Heat Shock Response in Caenorhabditis elegans Using Microarray Gene Expression and Computational Methods

  1. Debraj GuhaThakurta1,5,
  2. Lisanne Palomar1,
  3. Gary D. Stormo1,
  4. Pat Tedesco2,
  5. Thomas E. Johnson2,
  6. David W. Walker3,6,
  7. Gordon Lithgow3,7,
  8. Stuart Kim4, and
  9. Christopher D. Link2,8
  1. 1Department of Genetics, Washington University School of Medicine, St. Louis, Missouri 63114, USA; 2Institute for Behavioral Genetics, University of Colorado, Boulder, Colorado 80309, USA; 3School of Biological Sciences, University of Manchester, Manchester M13 9PT, United Kingdom; 4Department of Developmental Biology, Stanford University School of Medicine, Stanford, California 94305, USA.

Abstract

We report here the identification of a previously unknown transcription regulatory element for heat shock (HS) genes inCaenorhabditis elegans. We monitored the expression pattern of 11,917 genes from C. elegans to determine the genes that were up-regulated on HS. Twenty eight genes were observed to be consistently up-regulated in several different repetitions of the experiments. We analyzed the upstream regions of these genes using computational DNA pattern recognition methods. Two potential cis-regulatory motifs were identified in this way. One of these motifs (TTCTAGAA) was the DNA binding motif for the heat shock factor (HSF), whereas the other (GGGTGTC) was previously unreported in the literature. We determined the significance of these motifs for the HS genes using different statistical tests and parameters. Comparative sequence analysis of orthologous HS genes from C. elegans andCaenorhabditis briggsae indicated that the identified DNA regulatory motifs are conserved across related species. The role of the identified DNA sites in regulation of HS genes was tested by in vitro mutagenesis of a green fluorescent protein (GFP) reporter transgene driven by the C. elegans hsp-162promoter. DNA sites corresponding to both motifs are shown to play a significant role in up-regulation of the hsp-162gene on HS. This is one of the rare instances in which a novel regulatory element, identified using computational methods, is shown to be biologically active. The contributions of individual sites toward induction of transcription on HS are nonadditive, which indicates interaction and cross-talk between the sites, possibly through the transcription factors (TFs) binding to these sites.

[The following individuals kindly provided reagents, samples, or unpublished information as indicated in the paper: L. Hillier.]

Footnotes

  • Present addresses: 5Informatics Department, Rosetta Inpharmatics, Inc., 12040 115th Avenue, N.E., Kirkland. WA 98034, USA; 6Division of Biology, Caltech, Pasadena, CA 91125, USA; 7Buck Institute, 8001 Redwood Blvd., Novato, CA 94945, USA.

  • 8 Corresponding author.

  • E-MAIL linkc{at}colorado.edu; FAX (303) 492-8063.

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.228902.

    • Received December 18, 2001.
    • Accepted March 15, 2002.
| Table of Contents

Preprint Server