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


ABSTRACT: 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 Bmal1. We identify a non-canonical E-box element in Bmal1 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 (Tcap). 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.

SUBMITTER: Hodge BA 

PROVIDER: S-EPMC6398978 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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

Hodge Brian A BA   Zhang Xiping X   Gutierrez-Monreal Miguel A MA   Cao Yi Y   Hammers David W DW   Yao Zizhen Z   Wolff Christopher A CA   Du Ping P   Kemler Denise D   Judge Andrew R AR   Esser Karyn A KA  

eLife 20190221


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 <i>Bmal1</i>. We identify a non-canonical E-box element in <i>Bmal1</i> and demonstrate that is required for full MYOD1-responsiveness. Bimolecula  ...[more]

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