Genetic and epigenetic control of muscle development in vertebrates

Citation
B. Brand-saberi et B. Christ, Genetic and epigenetic control of muscle development in vertebrates, CELL TIS RE, 296(1), 1999, pp. 199-212
Citations number
180
Categorie Soggetti
Cell & Developmental Biology
Journal title
CELL AND TISSUE RESEARCH
ISSN journal
0302766X → ACNP
Volume
296
Issue
1
Year of publication
1999
Pages
199 - 212
Database
ISI
SICI code
0302-766X(199904)296:1<199:GAECOM>2.0.ZU;2-S
Abstract
The skeletal body muscle of vertebrates is derived from segmentally arrange d mesodermal structures, the somites. Only the dorsal epithelial half of th e somite, the dermomyotome, gives rise to muscle cells during normal develo pment. Head muscle takes its origin from the somites, the unsegmented parax ial head mesoderm and the prechordal mesoderm. Some muscle precursor cells, for instance those for limb and tongue muscle, migrate over considerable d istances before differentiating at their target sites. In recent years, our understanding of the molecular events underlying myogenesis has increased considerably. Muscle differentiation is preceded by several steps during wh ich precursor cells are specified. Markers of myogenic specification are my f5, myoD, mrf4 and myogenin, which encode transcription factors of the basi c helix-loop-helix family. These factors bind to promoters of many muscle-s pecific genes and interact with MEF2 (myocyte enhancer binding factor-2) be longing to the MADS (MCM1, agamous, deficiens, serum response factor) box t ranscription factors. Signalling events leading to myogenic precursor cell specification and to the formation of muscle fibres are being elucidated. I nductive signals emanate from the neural tube, notochord and ectoderm. Cont roversial findings concerning the role of the notochord and neural tube in muscle development suggest that the epigenetic events leading to myogenesis are more complex than originally anticipated. Signals from the lateral pla te counteract those from the axial organs and induce the locally restricted emigration of muscle precursor cells. Future investigations will have to s how how signalling molecules and their receptors interact in the process of fine-tuning muscle formation in the embryo.