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Conserved and divergent functions of Nfix in skeletal muscle development during vertebrate evolution
Author(s) -
Anna Pistocchi,
Germano Gaudenzi,
Efrem Alessandro Foglia,
Stefania Monteverde,
Artal MorenoFortuny,
Alessia Pianca,
Giulio Cossu,
Franco Cotelli,
Graziella Messina
Publication year - 2013
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.076315
Subject(s) - zebrafish , biology , myogenesis , microbiology and biotechnology , gene knockdown , vertebrate , skeletal muscle , motility , transcription factor , myocyte , gene , genetics , anatomy
During mouse skeletal muscle development, the Nfix gene has a pivotal role in regulating fetal-specific transcription. Zebrafish and mice share related programs for muscle development, although zebrafish develops at a much faster rate. In fact, although mouse fetal muscle fibers form after 15 days of development, in fish secondary muscle fibers form by 48 hours post-fertilization in a process that until now has been poorly characterized mechanically. In this work, we studied the zebrafish ortholog Nfix (nfixa) and its role in the proper switch to the secondary myogenic wave. This allowed us to highlight evolutionarily conserved and divergent functions of Nfix. In fact, the knock down of nfixa in zebrafish blocks secondary myogenesis, as in mouse, but also alters primary slow muscle fiber formation. Moreover, whereas Nfix mutant mice are motile, nfixa knockdown zebrafish display impaired motility that probably depends upon disruption of the sarcoplasmic reticulum. We conclude that, during vertebrate evolution, the transcription factor Nfix lost some specific functions, probably as a consequence of the different environment in which teleosts and mammals develop.

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