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Rho directs widespread termination of intragenic and stable RNA transcription

  • Jason M. Peters
  • , Rachel A. Mooney
  • , Pei Fen Kuan
  • , Jennifer L. Rowland
  • , Sündüz Keleş
  • , Robert Landick
  • University of Wisconsin-Madison

Research output: Contribution to journalArticlepeer-review

174 Scopus citations

Abstract

The transcription termination factor Rho is a global regulator of RNA polymerase (RNAP). Although individual Rho-dependent terminators have been studied extensively, less is known about the sites of RNAP regulation by Rho on a genome-wide scale. Using chromatin immunoprecipitation and microarrays (ChIP-chip), we examined changes in the distribution of Escherichia coli RNAP in response to the Rho-specific inhibitor bicyclomycin (BCM). We found ≈200 Rho-terminated loci that were divided evenly into 2 classes: intergenic (at the ends of genes) and intragenic (within genes). The intergenic class contained noncoding RNAs such as small RNAs (sRNAs) and transfer RNAs (tRNAs), establishing a previously unappreciated role of Rho in termination of stable RNA synthesis. The intragenic class of terminators included a previously uncharacterized set of short antisense transcripts, as judged by a shift in the distribution of RNAP in BCM-treated cells that was opposite to the direction of the corresponding gene. These Rho-terminated antisense transcripts point to a role of noncoding transcription in E. coli gene regulation that may resemble the ubiquitous noncoding transcription recently found to play myriad roles in eukaryotic gene regulation.

Original languageEnglish
Pages (from-to)15406-15411
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume106
Issue number36
DOIs
StatePublished - Sep 8 2009

Keywords

  • Chromatin immunoprecipitation
  • RNA polymerase

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