Literature DB >> 11456450

Hedgehog signalling is required for maintenance of myf5 and myoD expression and timely terminal differentiation in zebrafish adaxial myogenesis.

O Coutelle1, C S Blagden, R Hampson, C Halai, P W Rigby, S M Hughes.   

Abstract

Hedgehog proteins have been implicated in the control of myogenesis in the medial vertebrate somite. In the mouse, normal epaxial expression of the myogenic transcription factor gene myf5 is dependent on Sonic hedgehog. Here we examine in zebrafish the interaction between Hedgehog signals, the expression of myoD family genes, including the newly cloned zebrafish myf5, and slow myogenesis. We show that Sonic hedgehog is necessary for normal expression of both myf5 and myoD in adaxial slow muscle precursors, but not in lateral paraxial mesoderm. Expression of both genes is initiated normally in rostral presomitic mesoderm in sonic you mutants, which lack all Sonic hedgehog. Similar initiation continues during tailbud outgrowth when the cells forming caudal somites are generated. However, adaxial cells in sonic you embryos are delayed in terminal differentiation and caudal adaxial cells fail to maintain myogenic regulatory factor expression. Despite these defects, other signals are able to maintain, or reinitiate, some slow muscle development in sonic you mutants. In the cyclops mutant, the absence of floorplate-derived Tiggywinkle hedgehog and Sonic hedgehog has no discernible effect on slow adaxial myogenesis. Similarly, the absence of notochord-derived Sonic hedgehog and Echidna hedgehog in mutants lacking notochord delays, but does not prevent, adaxial slow muscle development. In contrast, removal of both Sonic hedgehog and a floorplate signal, probably Tiggywinkle hedgehog, from the embryonic midline in cyclops;sonic you double mutants essentially abolishes slow myogenesis. We conclude that several midline signals, likely to be various Hedgehogs, collaborate to maintain adaxial slow myogenesis in the zebrafish embryo. Moreover, the data demonstrate that, in the absence of this required Hedgehog signalling, expression of myf5 and myoD is insufficient to commit cells to adaxial myogenesis. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11456450     DOI: 10.1006/dbio.2001.0193

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  38 in total

1.  The initial somitic phase of Myf5 expression requires neither Shh signaling nor Gli regulation.

Authors:  Lydia Teboul; Dennis Summerbell; Peter W J Rigby
Journal:  Genes Dev       Date:  2003-12-01       Impact factor: 11.361

2.  Zebrafish foxc1a plays a crucial role in early somitogenesis by restricting the expression of aldh1a2 directly.

Authors:  Jingyun Li; Yunyun Yue; Xiaohua Dong; Wenshuang Jia; Kui Li; Dong Liang; Zhangji Dong; Xiaoxiao Wang; Xiaoxi Nan; Qinxin Zhang; Qingshun Zhao
Journal:  J Biol Chem       Date:  2015-02-27       Impact factor: 5.157

3.  Control of morphogenetic cell movements in the early zebrafish myotome.

Authors:  David F Daggett; Carmen R Domingo; Peter D Currie; Sharon L Amacher
Journal:  Dev Biol       Date:  2007-06-16       Impact factor: 3.582

4.  Differential requirements for myogenic regulatory factors distinguish medial and lateral somitic, cranial and fin muscle fibre populations.

Authors:  Yaniv Hinits; Daniel P S Osborn; Simon M Hughes
Journal:  Development       Date:  2009-02       Impact factor: 6.868

Review 5.  The notochord: structure and functions.

Authors:  Diana Corallo; Valeria Trapani; Paolo Bonaldo
Journal:  Cell Mol Life Sci       Date:  2015-04-02       Impact factor: 9.261

6.  Primary cilia control hedgehog signaling during muscle differentiation and are deregulated in rhabdomyosarcoma.

Authors:  Wenxiang Fu; Patrik Asp; Brian Canter; Brian David Dynlacht
Journal:  Proc Natl Acad Sci U S A       Date:  2014-06-09       Impact factor: 11.205

7.  In vitro indeterminate teleost myogenesis appears to be dependent on Pax3.

Authors:  Jacob Michael Froehlich; Nicholas J Galt; Matthew J Charging; Ben M Meyer; Peggy R Biga
Journal:  In Vitro Cell Dev Biol Anim       Date:  2013-04-24       Impact factor: 2.416

8.  Atoh8, a bHLH transcription factor, is required for the development of retina and skeletal muscle in zebrafish.

Authors:  Jihua Yao; Jingyao Zhou; Qiaoling Liu; Daru Lu; Lu Wang; Xiaojing Qiao; William Jia
Journal:  PLoS One       Date:  2010-06-03       Impact factor: 3.240

9.  Dynamic formation of microenvironments at the myotendinous junction correlates with muscle fiber morphogenesis in zebrafish.

Authors:  Chelsi J Snow; Clarissa A Henry
Journal:  Gene Expr Patterns       Date:  2008-08-26       Impact factor: 1.224

10.  Vestigial-like-2b (VITO-1b) and Tead-3a (Tef-5a) expression in zebrafish skeletal muscle, brain and notochord.

Authors:  Christopher J Mann; Daniel P S Osborn; Simon M Hughes
Journal:  Gene Expr Patterns       Date:  2007-08-15       Impact factor: 1.224

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