Mesogenin 1 is a master regulator of paraxial presomitic mesoderm differentiation
Author(s) -
Ravindra B. Chalamalasetty,
Robert J. Garriock,
William C. Dunty,
Mark W. Kennedy,
Parthav Jailwala,
Han Si,
Terry P. Yamaguchi
Publication year - 2014
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.110908
Subject(s) - paraxial mesoderm , biology , microbiology and biotechnology , regulator , somitogenesis , zebrafish , cellular differentiation , brachyury , transcription factor , neural tube , progenitor , hindbrain , stem cell , mesoderm , genetics , progenitor cell , somite , embryonic stem cell , embryo , gene , embryogenesis
Neuromesodermal (NM) stem cells generate neural and paraxial presomitic mesoderm (PSM) cells, which are the respective progenitors of the spinal cord and musculoskeleton of the trunk and tail. The Wnt-regulated basic helix-loop-helix (bHLH) transcription factor mesogenin 1 (Msgn1) has been implicated as a cooperative regulator working in concert with T-box genes to control PSM formation in zebrafish, although the mechanism is unknown. We show here that, in mice, Msgn1 alone controls PSM differentiation by directly activating the transcriptional programs that define PSM identity, epithelial-mesenchymal transition, motility and segmentation. Forced expression of Msgn1 in NM stem cells in vivo reduced the contribution of their progeny to the neural tube, and dramatically expanded the unsegmented mesenchymal PSM while blocking somitogenesis and notochord differentiation. Expression of Msgn1 was sufficient to partially rescue PSM differentiation in Wnt3a(-/-) embryos, demonstrating that Msgn1 functions downstream of Wnt3a as the master regulator of PSM differentiation. Our data provide new insights into how cell fate decisions are imposed by the expression of a single transcriptional regulator.
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