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Topology and Control of the Cell-Cycle-Regulated Transcriptional Circuitry

Journal

GENETICS
Volume 196, Issue 1, Pages 65-90

Publisher

GENETICS SOCIETY AMERICA
DOI: 10.1534/genetics.113.152595

Keywords

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Funding

  1. Defense Advanced Research Projects Agency
  2. National Institutes of Health (NIH) [P50-GM081883]
  3. National Institutes of Health [R01 GM059441, R01 GM100354]

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Nearly 20% of the budding yeast genome is transcribed periodically during the cell division cycle. The precise temporal execution of this large transcriptional program is controlled by a large interacting network of transcriptional regulators, kinases, and ubiquitin ligases. Historically, this network has been viewed as a collection of four coregulated gene clusters that are associated with each phase of the cell cycle. Although the broad outlines of these gene clusters were described nearly 20 years ago, new technologies have enabled major advances in our understanding of the genes comprising those clusters, their regulation, and the complex regulatory interplay between clusters. More recently, advances are being made in understanding the roles of chromatin in the control of the transcriptional program. We are also beginning to discover important regulatory interactions between the cell-cycle transcriptional program and other cell-cycle regulatory mechanisms such as checkpoints and metabolic networks. Here we review recent advances and contemporary models of the transcriptional network and consider these models in the context of eukaryotic cell-cycle controls.

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