Letter abstract


Nature Genetics 39, 1507 - 1511 (2007)
Published online: 11 November 2007 | doi:10.1038/ng.2007.21

RNA polymerase is poised for activation across the genome

Ginger W Muse1, Daniel A Gilchrist1, Sergei Nechaev1, Ruchir Shah2, Joel S Parker2,4, Sherry F Grissom3, Julia Zeitlinger5,6 & Karen Adelman1

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Regulation of gene expression is integral to the development and survival of all organisms. Transcription begins with the assembly of a pre-initiation complex at the gene promoter1, followed by initiation of RNA synthesis and the transition to productive elongation2, 3, 4. In many cases, recruitment of RNA polymerase II (Pol II) to a promoter is necessary and sufficient for activation of genes. However, there are a few notable exceptions to this paradigm, including heat shock genes and several proto-oncogenes, whose expression is attenuated by regulated stalling of polymerase elongation within the promoter-proximal region5, 6, 7, 8, 9, 10, 11, 12, 13. To determine the importance of polymerase stalling for transcription regulation, we carried out a genome-wide search for Drosophila melanogaster genes with Pol II stalled within the promoter-proximal region. Our data show that stalling is widespread, occurring at hundreds of genes that respond to stimuli and developmental signals. This finding indicates a role for regulation of polymerase elongation in the transcriptional responses to dynamic environmental and developmental cues.

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  1. Laboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.
  2. Constella Group, 2605 Meridian Parkway, Suite 200, Durham, North Carolina 27713, USA.
  3. Microarray Group, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.
  4. Expression Analysis, 4312 South Alston Ave., Durham, North Carolina 27713, USA.
  5. Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, Massachusetts 02142, USA.
  6. Stowers Institute for Medical Research, 1000 East 50th St., Kansas City, Missouri 64110, USA.

Correspondence to: Karen Adelman1 e-mail: adelmank@niehs.nih.gov



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