Differential effects of light and feeding on circadian organization of peripheral clocks in a forebrain Bmal1 mutant

Author:

Izumo Mariko1,Pejchal Martina2,Schook Andrew C23,Lange Ryan P2,Walisser Jacqueline A4,Sato Takashi R56,Wang Xiaozhong7,Bradfield Christopher A4,Takahashi Joseph S18ORCID

Affiliation:

1. Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, United States

2. Department of Neurobiology, Northwestern University, Evanston, United States

3. Howard Hughes Medical Institute, Northwestern University, Evanston, United States

4. McArdle Laboratory for Cancer Research, University of Wisconsin, Madison, United States

5. Werner Reichardt Centre for Integrative Neuroscience, University of Tübingen, Tübingen, Germany

6. JST, PRESTO, University of Tübingen, Tübingen, Germany

7. Department of Molecular Biosciences, Northwestern University, Evanston, United States

8. Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, United States

Abstract

In order to assess the contribution of a central clock in the hypothalamic suprachiasmatic nucleus (SCN) to circadian behavior and the organization of peripheral clocks, we generated forebrain/SCN-specific Bmal1 knockout mice by using floxed Bmal1 and pan-neuronal Cre lines. The forebrain knockout mice showed >90% deletion of BMAL1 in the SCN and exhibited an immediate and complete loss of circadian behavior in constant conditions. Circadian rhythms in peripheral tissues persisted but became desynchronized and damped in constant darkness. The loss of synchrony was rescued by light/dark cycles and partially by restricted feeding (only in the liver and kidney but not in the other tissues) in a distinct manner. These results suggest that the forebrain/SCN is essential for internal temporal order of robust circadian programs in peripheral clocks, and that individual peripheral clocks are affected differently by light and feeding in the absence of a functional oscillator in the forebrain.

Funder

Howard Hughes Medical Institute

National Institute of Mental Health

National Institute of Neurological Disorders and Stroke

Brain and Behavior Research Foundation

National Institute of Environmental Health Sciences

Japan Science and Technology Agency

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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