Literature DB >> 27144473

Barx2 and Pax7 Regulate Axin2 Expression in Myoblasts by Interaction with β-Catenin and Chromatin Remodelling.

Julie-Ann Hulin1, Thi Diem Tran Nguyen1,2, Shuang Cui1, Shashikanth Marri3, Ruth T Yu4, Michael Downes4, Ronald M Evans4,5, Helen Makarenkova6, Robyn Meech1.   

Abstract

Satellite cells are the resident stem cells of skeletal muscle; quiescent in adults until activated by injury to generate proliferating myoblasts. The canonical Wnt signalling pathway, mediated by T-cell factor/lymphoid enhancer factor (TCF/LEF) and β-catenin effector proteins, controls myoblast differentiation in vitro, and recent work suggests that timely termination of the Wnt/β-catenin signal is important for normal adult myogenesis. We recently identified the Barx2 and Pax7 homeobox proteins as novel components of the Wnt effector complex. Here, we examine molecular and epigenetic mechanisms by which Barx2 and Pax7 regulate the canonical Wnt target gene Axin2, which mediates critical feedback to terminate the transcriptional response to Wnt signals. Barx2 is recruited to the Axin2 gene via TCF/LEF binding sites, recruits β-catenin and the coactivator GRIP-1, and induces local H3K-acetylation. Barx2 also promotes nuclear localization of β-catenin. Conversely, Pax7 represses Axin2 promoter/intron activity and inhibits Barx2-mediated H3K-acetylation via the corepressor HDAC1. Wnt3a not only induces Barx2 mRNA, but also stabilises Barx2 protein in myoblasts; conversely, Wnt3a potently inhibits Pax7 protein expression. As Barx2 promotes myogenic differentiation and Pax7 suppresses it, this novel posttranscriptional regulation of Barx2 and Pax7 by Wnt3a may be involved in the specification of differentiation-competent and -incompetent myoblast populations. Finally, we propose a model for dual function of Barx2 downstream of Wnt signals: activation of myogenic target genes in association with canonical myogenic regulatory factors, and regulation of the negative feedback loop that limits the response of myoblasts to Wnt signals via direct interaction of Barx2 with the TCF/β-catenin complex. Stem Cells 2016;34:2169-2182.
© 2016 AlphaMed Press.

Entities:  

Keywords:  Cell signalling; Differentiation; Epigenetics; Homeobox genes; Muscle stem cells; Myogenesis; Skeletal muscle; Transcription factors

Mesh:

Substances:

Year:  2016        PMID: 27144473      PMCID: PMC5019118          DOI: 10.1002/stem.2396

Source DB:  PubMed          Journal:  Stem Cells        ISSN: 1066-5099            Impact factor:   5.845


  65 in total

1.  Pax7 and myogenic progression in skeletal muscle satellite cells.

Authors:  Peter S Zammit; Frederic Relaix; Yosuke Nagata; Ana Pérez Ruiz; Charlotte A Collins; Terence A Partridge; Jonathan R Beauchamp
Journal:  J Cell Sci       Date:  2006-04-11       Impact factor: 5.285

2.  Wnt/beta-catenin/Tcf signaling induces the transcription of Axin2, a negative regulator of the signaling pathway.

Authors:  Eek-hoon Jho; Tong Zhang; Claire Domon; Choun-Ki Joo; Jean-Noel Freund; Frank Costantini
Journal:  Mol Cell Biol       Date:  2002-02       Impact factor: 4.272

3.  A temporal switch from notch to Wnt signaling in muscle stem cells is necessary for normal adult myogenesis.

Authors:  Andrew S Brack; Irina M Conboy; Michael J Conboy; Jeanne Shen; Thomas A Rando
Journal:  Cell Stem Cell       Date:  2008-01-10       Impact factor: 24.633

Review 4.  Mechanisms of Wnt signaling in development.

Authors:  A Wodarz; R Nusse
Journal:  Annu Rev Cell Dev Biol       Date:  1998       Impact factor: 13.827

5.  The transcriptional coactivators p300 and CBP are histone acetyltransferases.

Authors:  V V Ogryzko; R L Schiltz; V Russanova; B H Howard; Y Nakatani
Journal:  Cell       Date:  1996-11-29       Impact factor: 41.582

6.  The homeodomain protein Barx2 contains activator and repressor domains and interacts with members of the CREB family.

Authors:  D B Edelman; R Meech; F S Jones
Journal:  J Biol Chem       Date:  2000-07-14       Impact factor: 5.157

7.  Wnt4 activates the canonical β-catenin pathway and regulates negatively myostatin: functional implication in myogenesis.

Authors:  Henri Bernardi; Stephanie Gay; Yann Fedon; Barbara Vernus; Anne Bonnieu; Francis Bacou
Journal:  Am J Physiol Cell Physiol       Date:  2011-01-19       Impact factor: 4.249

8.  The homeobox transcription factor Barx2 regulates plasticity of young primary myofibers.

Authors:  Robyn Meech; Mariana Gomez; Christopher Woolley; Marietta Barro; Julie-Ann Hulin; Elisabeth C Walcott; Jary Delgado; Helen P Makarenkova
Journal:  PLoS One       Date:  2010-07-15       Impact factor: 3.240

9.  Wingless signaling induces widespread chromatin remodeling of target loci.

Authors:  David S Parker; Yunyun Y Ni; Jinhee L Chang; Jiong Li; Ken M Cadigan
Journal:  Mol Cell Biol       Date:  2007-12-26       Impact factor: 4.272

10.  Synergistic effects of coactivators GRIP1 and beta-catenin on gene activation: cross-talk between androgen receptor and Wnt signaling pathways.

Authors:  Hongwei Li; Jeong Hoon Kim; Stephen S Koh; Michael R Stallcup
Journal:  J Biol Chem       Date:  2003-11-24       Impact factor: 5.157

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1.  Circular RNA circSHPRH inhibits the malignant behaviors of bladder cancer by regulating the miR-942/BARX2 pathway.

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2.  β-Catenin is essential for differentiation of primary myoblasts via cooperation with MyoD and α-catenin.

Authors:  Shuang Cui; Liang Li; Ruth T Yu; Michael Downes; Ronald M Evans; Julie-Ann Hulin; Helen P Makarenkova; Robyn Meech
Journal:  Development       Date:  2019-03-19       Impact factor: 6.868

3.  S100A4 promotes lung tumor development through β-catenin pathway-mediated autophagy inhibition.

Authors:  Shasha Hou; Tian Tian; Dianwen Qi; Kaiji Sun; Qi Yuan; Ziling Wang; Zhihai Qin; Zhenlong Wu; Zhinan Chen; Jinhua Zhang
Journal:  Cell Death Dis       Date:  2018-02-15       Impact factor: 8.469

4.  The interaction of canonical Wnt/β-catenin signaling with protein lysine acetylation.

Authors:  Hongjuan You; Qi Li; Delong Kong; Xiangye Liu; Fanyun Kong; Kuiyang Zheng; Renxian Tang
Journal:  Cell Mol Biol Lett       Date:  2022-01-15       Impact factor: 5.787

5.  Functional high-throughput screen identifies microRNAs that promote butyrate-induced death in colorectal cancer cells.

Authors:  Saira R Ali; Karen J Humphreys; Kaylene J Simpson; Ross A McKinnon; Robyn Meech; Michael Z Michael
Journal:  Mol Ther Nucleic Acids       Date:  2022-08-29       Impact factor: 10.183

Review 6.  Histone acetylation dynamics in repair of DNA double-strand breaks.

Authors:  Shalini Aricthota; Paresh Priyadarshan Rana; Devyani Haldar
Journal:  Front Genet       Date:  2022-09-09       Impact factor: 4.772

7.  A Type 2 Deiodinase-Dependent Increase in Vegfa Mediates Myoblast-Endothelial Cell Crosstalk During Skeletal Muscle Regeneration.

Authors:  Xingxing An; Ashley Ogawa-Wong; Colleen Carmody; Raffaele Ambrosio; Annunziata Gaetana Cicatiello; Cristina Luongo; Domenico Salvatore; Diane E Handy; P Reed Larsen; Simone Magagnin Wajner; Monica Dentice; Ann Marie Zavacki
Journal:  Thyroid       Date:  2020-09-09       Impact factor: 6.568

8.  MicroRNA induction by copy number gain is associated with poor outcome in squamous cell carcinoma of the lung.

Authors:  Endi Xia; Sotaro Kanematsu; Yusuke Suenaga; Asmaa Elzawahry; Hitomi Kondo; Noriko Otsuka; Yasumitsu Moriya; Toshihiko Iizasa; Mamoru Kato; Ichiro Yoshino; Sana Yokoi
Journal:  Sci Rep       Date:  2018-10-18       Impact factor: 4.379

  8 in total

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