Literature DB >> 22522309

Non conservation of function for the evolutionarily conserved prdm1 protein in the control of the slow twitch myogenic program in the mouse embryo.

Stéphane D Vincent1, Alicia Mayeuf, Claire Niro, Mitinori Saitou, Margaret Buckingham.   

Abstract

Muscles are composed of multinucleated muscle fibers with different contractile and physiological properties, which result from specific slow or fast gene expression programs in the differentiated muscle cells. In the zebra fish embryo, the slow program is under the control of Hedgehog signaling from the notochord and floor plate. This pathway activates the expression of the conserved transcriptional repressor, Prdm1 (Blimp1), which in turn represses the fast program and promotes the slow program in adaxial cells of the somite and their descendants. In the mouse embryo, myogenesis is also initiated in the myotomal compartment of the somite, but the slow muscle program is not confined to a specific subset of cells. We now show that Prdm1 is expressed in the first differentiated myocytes of the early myotome from embryonic day (E)9.5-E11.5. During this period, muscle formation depends on the myogenic regulatory factors, Myf5 and Mrf4. In their absence, Prdm1 is not activated, in apparent contrast to zebra fish where Prdm1 is expressed in the absence of Myf5 and MyoD that drive myogenesis in adaxial cells. However, as in zebra fish, Prdm1 expression in the mouse myotome does not occur in the absence of Hedgehog signaling. Analysis of the muscle phenotype of Prdm1 mutant embryos shows that myogenesis appears to proceed normally. Notably, there is no requirement for Prdm1 activation of the slow muscle program in the mouse myotome. Furthermore, the gene for the transcriptional repressor, Sox6, which is repressed by Prdm1 to permit slow muscle differentiation in zebra fish, is not expressed in the mouse myotome. We propose that the lack of functional conservation for mouse Prdm1, that can nevertheless partially rescue the adaxial cells of zebra fish Prdm1 mutants, reflects differences in the evolution of the role of key regulators such as Prdm1 or Sox6, in initiating the onset of the slow muscle program, between teleosts and mammals.

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Year:  2012        PMID: 22522309     DOI: 10.1093/molbev/mss125

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  11 in total

1.  Prdm12 specifies V1 interneurons through cross-repressive interactions with Dbx1 and Nkx6 genes in Xenopus.

Authors:  Aurore Thélie; Simon Desiderio; Julie Hanotel; Ian Quigley; Benoit Van Driessche; Anthony Rodari; Mark D Borromeo; Sadia Kricha; François Lahaye; Jenifer Croce; Gustavo Cerda-Moya; Jesús Ordoño Fernandez; Barbara Bolle; Katharine E Lewis; Maike Sander; Alessandra Pierani; Michael Schubert; Jane E Johnson; Christopher R Kintner; Tomas Pieler; Carine Van Lint; Kristine A Henningfeld; Eric J Bellefroid; Claude Van Campenhout
Journal:  Development       Date:  2015-10-01       Impact factor: 6.868

2.  Temporal analysis of reciprocal miRNA-mRNA expression patterns predicts regulatory networks during differentiation in human skeletal muscle cells.

Authors:  Rasmus J O Sjögren; Brendan Egan; Mutsumi Katayama; Juleen R Zierath; Anna Krook
Journal:  Physiol Genomics       Date:  2014-12-29       Impact factor: 3.107

Review 3.  Skeletal muscle fiber type: using insights from muscle developmental biology to dissect targets for susceptibility and resistance to muscle disease.

Authors:  Jared Talbot; Lisa Maves
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2016-05-19       Impact factor: 5.814

4.  The miRNA Transcriptome Directly Reflects the Physiological and Biochemical Differences between Red, White, and Intermediate Muscle Fiber Types.

Authors:  Jideng Ma; Hongmei Wang; Rui Liu; Long Jin; Qianzi Tang; Xun Wang; Anan Jiang; Yaodong Hu; Zongwen Li; Li Zhu; Ruiqiang Li; Mingzhou Li; Xuewei Li
Journal:  Int J Mol Sci       Date:  2015-04-29       Impact factor: 5.923

5.  Nfix Induces a Switch in Sox6 Transcriptional Activity to Regulate MyHC-I Expression in Fetal Muscle.

Authors:  Valentina Taglietti; Giovanni Maroli; Solei Cermenati; Stefania Monteverde; Andrea Ferrante; Giuliana Rossi; Giulio Cossu; Monica Beltrame; Graziella Messina
Journal:  Cell Rep       Date:  2016-11-22       Impact factor: 9.423

6.  Loss of Prox1 in striated muscle causes slow to fast skeletal muscle fiber conversion and dilated cardiomyopathy.

Authors:  Louisa K Petchey; Catherine A Risebro; Joaquim M Vieira; Tom Roberts; John B Bryson; Linda Greensmith; Mark F Lythgoe; Paul R Riley
Journal:  Proc Natl Acad Sci U S A       Date:  2014-06-17       Impact factor: 11.205

7.  Pbx and Prdm1a transcription factors differentially regulate subsets of the fast skeletal muscle program in zebrafish.

Authors:  Zizhen Yao; Gist H Farr; Stephen J Tapscott; Lisa Maves
Journal:  Biol Open       Date:  2013-04-08       Impact factor: 2.422

8.  The PR/SET domain zinc finger protein Prdm4 regulates gene expression in embryonic stem cells but plays a nonessential role in the developing mouse embryo.

Authors:  Debora Bogani; Marc A J Morgan; Andrew C Nelson; Ita Costello; Joanna F McGouran; Benedikt M Kessler; Elizabeth J Robertson; Elizabeth K Bikoff
Journal:  Mol Cell Biol       Date:  2013-08-05       Impact factor: 4.272

9.  Expression patterns of prdm1 during chicken embryonic and germline development.

Authors:  Zhiyi Wan; Lei Rui; Zandong Li
Journal:  Cell Tissue Res       Date:  2014-04-02       Impact factor: 5.249

Review 10.  Comparative myogenesis in teleosts and mammals.

Authors:  Giuliana Rossi; Graziella Messina
Journal:  Cell Mol Life Sci       Date:  2014-03-25       Impact factor: 9.261

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