Corinne A Betts
Dystrophin regulates peripheral circadian SRF signalling
Betts, Corinne A; Jagannath, Aarti; van Westering, Tirsa LE; Bowerman, Melissa; Banerjee, Subhashis; Meng, Jinhong; Falzarano, Maria Sofia; Cravo, Lara; McClorey, Graham; Meijboom, Katharina E; Bhomra, Amarjit; Fang Lim, Wooi; Rinaldi, Carlo; Counsell, John R; Chwalenia, Katarzyna; O’Donovan, Elizabeth; Saleh, Amer F; Gait, Michael J; Morgan, Jennifer E; Ferlini, Alessandra; Foster, Russell G; Wood, Matthew JA
Authors
Aarti Jagannath
Tirsa LE van Westering
Melissa Bowerman m.bowerman@keele.ac.uk
Subhashis Banerjee
Jinhong Meng
Maria Sofia Falzarano
Lara Cravo
Graham McClorey
Katharina E Meijboom
Amarjit Bhomra
Wooi Fang Lim
Carlo Rinaldi
John R Counsell
Katarzyna Chwalenia
Elizabeth O’Donovan
Amer F Saleh
Michael J Gait
Jennifer E Morgan
Alessandra Ferlini
Russell G Foster
Matthew JA Wood
Abstract
Dystrophin is a sarcolemmal protein essential for muscle contraction and maintenance, absence of which leads to the devastating muscle wasting disease Duchenne muscular dystrophy (DMD)[1, 2]. Dystrophin has an actin-binding domain [3–5], which specifically binds and stabilises filamentous (F)-actin[6], an integral component of the RhoA-actin-serum response factor (SRF)-pathway[7]. The RhoA-actin-SRF-pathway plays an essential role in circadian signalling whereby the hypothalamic suprachiasmatic nucleus, transmits systemic cues to peripheral tissues, activating SRF and transcription of clock target genes[8, 9]. Given dystrophin binds F-actin and disturbed SRF-signalling disrupts clock entrainment, we hypothesised that dystrophin loss causes circadian deficits. Here we show for the first time alterations in the RhoA-actin-SRF-signalling-pathway, in both dystrophin-deficient myotubes and dystrophic mouse models. Specifically, we demonstrate reduced F/G-actin ratios and nuclear MRTF, dysregulation of core clock and downstream target-genes, and down-regulation of key circadian genes in muscle biopsies from DMD patients harbouring an array of mutations. Further, disrupted circadian locomotor behaviour was observed in dystrophic mice indicative of disrupted SCN signalling, and indeed dystrophin protein was absent in the SCN of dystrophic animals. Dystrophin is thus a critically important component of the RhoA-actin-SRF-pathway and a novel mediator of circadian signalling in peripheral tissues, loss of which leads to circadian dysregulation.
Citation
Betts, C. A., Jagannath, A., van Westering, T. L., Bowerman, M., Banerjee, S., Meng, J., Falzarano, M. S., Cravo, L., McClorey, G., Meijboom, K. E., Bhomra, A., Fang Lim, W., Rinaldi, C., Counsell, J. R., Chwalenia, K., O’Donovan, E., Saleh, A. F., Gait, M. J., Morgan, J. E., Ferlini, A., …Wood, M. J. (2021). Dystrophin regulates peripheral circadian SRF signalling
Other Type | Other |
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Acceptance Date | Jun 23, 2021 |
Publication Date | Jun 23, 2021 |
Publisher | Cold Spring Harbor Laboratory Press |
DOI | https://doi.org/10.1101/2021.06.23.449492 |
Public URL | https://keele-repository.worktribe.com/output/425175 |
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Publisher Licence URL
https://creativecommons.org/licenses/by-nc/4.0/
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