A genomewide oscillation in transcription gates DNA replication and cell cycle

  1. Robert R. Klevecz*,
  2. James Bolen,
  3. Gerald Forrest, and
  4. Douglas B. Murray
  1. Dynamics Group, Department of Biology, Beckman Research Institute of the City of Hope Medical Center, Duarte, CA 91010
  1. Edited by Steven L. McKnight, University of Texas Southwestern Medical Center, Dallas, TX, and approved November 26, 2003 (received for review October 7, 2003)

Abstract

Microarray analysis from a yeast continuous synchrony culture system shows a genomewide oscillation in transcription. Maximums in transcript levels occur at three nearly equally spaced intervals in this ≈40-min cycle of respiration and reduction. Two temporal clusters (4,679 of 5,329) are maximally expressed during the reductive phase of the cycle, whereas a third cluster (650) is maximally expressed during the respiratory phase. Transcription is organized functionally into redox-state superclusters with genes known to be important in respiration or reduction being synthesized in opposite phases of the cycle. The transcriptional cycle gates synchronous bursts in DNA replication in a constant fraction of the population at 40-min intervals. Restriction of DNA synthesis to the reductive phase of the cycle may be an evolutionarily important mechanism for reducing oxidative damage to DNA during replication.

Footnotes

  • * To whom correspondence should be addressed. E-mail: rklevecz{at}coh.org.

  • This paper was submitted directly (Track II) to the PNAS office.

  • Abbreviation: DO, dissolved oxygen.

  • See Commentary on page 1118.

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