Six1 regulates proliferation of Pax7-positive muscle progenitors in zebrafish

Abstract

In the embryonic zebrafish, skeletal muscle fibres are formed from muscle progenitors in the paraxial mesoderm. The embryonic myotome is mostly constituted of fast-twitch-specific fibres, which are formed from a fast-specific progenitor cell pool. The most lateral fraction of the fast domain in the myotome of zebrafish embryos derives from the Pax7-positive dermomyotome-like cells. I this study, we show that two genes, belonging to the sine oculus class 1 (six1) genes (six1a and six1b), are both essential for the regulation of Pax7+ cell proliferation and, consequently, in their differentiation during the establishment of the zebrafish dermomyotome. In both six1a and six1bmorphant embryos, Pax7+ cells are initially formed but fail to proliferate, as detected by reducedlevels of the proliferation marker phosphohistone3 and reduced brdU incorporation. In congruence, overexpression of six1a or six1b leads to increased Pax7+ cell number and reduced or alternativelydelayed fibre cell differentiation. Bone morphogenetic protein signalling has previously been suggested to inhibit differentiation of Pax7+ cells in the dermomyotome. Here we show that the remaining Pax7+cells in six1a and six1b morphant embryos also have significantly reduced pSmad1/5/8 levels and propose that this leads to a reduced proliferative activity, which may result in a premature differentiation of Pax7+ cells in the zebrafish dermomyotome. In summary, we show a mechanism for Six1a and Six1b in establishing the Pax7+ cell derived part of the fast muscle and suggest new important roles for Six1 in the regulation of the Pax7+ musclecell population through pSmad1/5/8 signalling. © 2013. Published by The Company of Biologists Ltd.