Rev-erbα dynamically modulates chromatin looping to control circadian gene transcription

Author:

Kim Yong Hoon123ORCID,Marhon Sajid A.123ORCID,Zhang Yuxiang12ORCID,Steger David J.12ORCID,Won Kyoung-Jae123ORCID,Lazar Mitchell A.123ORCID

Affiliation:

1. Institute for Diabetes, Obesity, and Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

2. Division of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

3. Department of Genetics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

Abstract

Chromosome dynamics and cellular clocks Many genes undergo daily or circadian changes in their rate of transcription. Kim et al. explored the mechanism by which the circadian clock is linked to chromosome dynamics (see the Perspective by Diettrich Mallet de Lima and Göndör). They used a chromosome conformation capture technique (Hi-C) to identify the interactions of adjacent DNA fragments and determine how DNA looping that altered such interactions changed over daily cycles. The repressive transcription factor Rev-erbα, which functions as part of the mammalian clock mechanism, appears to bind to chromatin and recruit a protein complex that evicts other proteins that enhance looping, thus favoring enhancer-promoter interactions. Science , this issue p. 1274 ; see also p. 1212

Funder

NIH

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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