Mitotic transcription and waves of gene reactivation during mitotic exit

Author:

Palozola Katherine C.12ORCID,Donahue Greg2,Liu Hong3,Grant Gregory R.4,Becker Justin S.12ORCID,Cote Allison5ORCID,Yu Hongtao6ORCID,Raj Arjun5ORCID,Zaret Kenneth S.12ORCID

Affiliation:

1. Institute for Regenerative Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-5157, USA.

2. Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-5157, USA.

3. Department of Biochemistry and Molecular Biology and Tulane Center for Aging, Tulane University Health Sciences Center, New Orleans, LA 70112, USA.

4. The Institute for Translational Medicine and Therapeutics, Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

5. Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104, USA.

6. Howard Hughes Medical Institute, Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

Abstract

Gene expression during mitosis During mitosis, long-range interactions within chromosomes are lost, and many enhancers become inactive. It is generally thought that gene expression is silent at this time. However, transcription must be reactivated when cells reenter the cell cycle in order to maintain cell identity. Palozola et al. used a sensitive nascent RNA labeling and sequencing method to reveal low-level transcription of many genes in mitosis. Upon mitotic exit, the amplitude of gene expression was reestablished with basic cell functions prioritized over cell-specific genes. Thus, transcription itself may retain gene expression patterns through mitosis. Science , this issue p. 119

Funder

NIH Office of the Director

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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