Citation

Falick Michaeli T, Sabag O, Fok R, Azria B, Monin J, Nevo Y, Gielchinsky Y, Berman BP, Cedar H, Bergman Y. Proc. Natl. Acad. Sci. U. S. A. 2022; 119(52): e2212306119.

Copyright

(Copyright © 2022, National Academy of Sciences)

DOI

10.1073/pnas.2212306119

PMID

36534800

Abstract

Injury to muscle brings about the activation of stem cells, which then generate new myocytes to replace damaged tissue. We demonstrate that this activation is accompanied by a dramatic change in the stem-cell methylation pattern that prepares them epigenetically for terminal myocyte differentiation. These de- and de novo methylation events occur at regulatory elements associated with genes involved in myogenesis and are necessary for activation and regeneration. Local injury of one muscle elicits an almost identical epigenetic change in satellite cells from other muscles in the body, in a process mediated by circulating factors. Furthermore, this same methylation state is also generated in muscle stem cells (MuSCs) of female animals following pregnancy, even in the absence of any injury. Unlike the activation-induced expression changes, which are transient, the induced methylation profile is stably maintained in resident MuSCs and thus represents a molecular memory of previous physiological events that is probably programmed to provide a mechanism for long-term adaptation.

Language: en

Keywords

development; priming; epigenetics