Per1/Per2–Igf2 axis–mediated circadian regulation of myogenic differentiation

Author:

Katoku-Kikyo Nobuko12ORCID,Paatela Ellen12ORCID,Houtz Daniel L.1ORCID,Lee Britney1ORCID,Munson Dane1,Wang Xuerui134ORCID,Hussein Mohammed134ORCID,Bhatia Jasmeet134ORCID,Lim Seunghyun15,Yuan Ce15ORCID,Asakura Yoko134ORCID,Asakura Atsushi134ORCID,Kikyo Nobuaki12ORCID

Affiliation:

1. Stem Cell Institute, University of Minnesota, Minneapolis, MN

2. Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN

3. Paul & Sheila Wellstone Muscular Dystrophy Center, University of Minnesota, Minneapolis, MN

4. Department of Neurology, University of Minnesota, Minneapolis, MN

5. Bioinformatics and Computational Biology Graduate Program, University of Minnesota, Minneapolis, MN

Abstract

Circadian rhythms regulate cell proliferation and differentiation, but circadian control of tissue regeneration remains elusive at the molecular level. Here, we show that proper myoblast differentiation and muscle regeneration are regulated by the circadian master regulators Per1 and Per2. Depletion of Per1 or Per2 suppressed myoblast differentiation in vitro and muscle regeneration in vivo, demonstrating their nonredundant functions. Both Per1 and Per2 were required for the activation of Igf2, an autocrine promoter of myoblast differentiation, accompanied by Per-dependent recruitment of RNA polymerase II, dynamic histone modifications at the Igf2 promoter and enhancer, and the promoter–enhancer interaction. This circadian epigenetic priming created a preferred time window for initiating myoblast differentiation. Consistently, muscle regeneration was faster if initiated at night, when Per1, Per2, and Igf2 were highly expressed compared with morning. This study reveals the circadian timing as a significant factor for effective muscle cell differentiation and regeneration.

Funder

Minnesota Stem Cell Institute

National Institutes of Health

Regenerative Medicine Minnesota

University of Minnesota

Publisher

Rockefeller University Press

Subject

Cell Biology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3