MYOD1 functions as a clock amplifier as well as a critical co-factor for downstream circadian gene expression in muscle

In the present study we show that the master myogenic regulatory factor, MYOD1, is a positive modulator of molecular clock amplitude and functions with the core clock factors for expression of clock-controlled genes in skeletal muscle. We demonstrate that MYOD1 directly regulates the expression and...

Full description

Saved in:
Bibliographic Details
Published ineLife Vol. 8
Main Authors Hodge, Brian A, Zhang, Xiping, Gutierrez-Monreal, Miguel A, Cao, Yi, Hammers, David W, Yao, Zizhen, Wolff, Christopher A, Du, Ping, Kemler, Denise, Judge, Andrew R, Esser, Karyn A
Format Journal Article
LanguageEnglish
Published England eLife Science Publications, Ltd 21.02.2019
eLife Sciences Publications Ltd
eLife Sciences Publications, Ltd
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:In the present study we show that the master myogenic regulatory factor, MYOD1, is a positive modulator of molecular clock amplitude and functions with the core clock factors for expression of clock-controlled genes in skeletal muscle. We demonstrate that MYOD1 directly regulates the expression and circadian amplitude of the positive core clock factor . We identify a non-canonical E-box element in and demonstrate that is required for full MYOD1-responsiveness. Bimolecular fluorescence complementation assays demonstrate that MYOD1 colocalizes with both BMAL1 and CLOCK throughout myonuclei. We demonstrate that MYOD1 and BMAL1:CLOCK work in a synergistic fashion through a tandem E-box to regulate the expression and amplitude of the muscle specific clock-controlled gene, Titin-cap ( ). In conclusion, these findings reveal mechanistic roles for the muscle specific transcription factor MYOD1 in the regulation of molecular clock amplitude as well as synergistic regulation of clock-controlled genes in skeletal muscle.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
These authors contributed equally to this work.
Buck Institute for Research on Aging, Novato, United States.
ISSN:2050-084X
2050-084X
DOI:10.7554/elife.43017