Literature DB >> 20063414

Characterization of genomic structures and expression profiles of three tandem repeats of a mouse double homeobox gene: Duxbl.

Shey-Lin Wu1, Ming-Shiun Tsai, Swee-Hee Wong, Hsiu-Mei Hsieh-Li, Tz-Shiu Tsai, Wei-Tang Chang, Shin-Ling Huang, Chun-Ching Chiu, Sue-Hong Wang.   

Abstract

We identified and cloned a mouse double homeobox gene (Duxbl), which encodes two homeodomains. Duxbl gene, a tandem triplicate produces two major transcripts, Duxbl and Duxbl-s. The amino acid sequences of Duxbl homeodomains are most similar to those of human DUX4 protein, associated with facioscapulohumeral muscular dystrophy. In adult tissues, Duxbl is predominantly expressed in female reproductive organs and eyes, and slightly expressed in brain and testes. During gonad development, Duxbl is expressed from embryonic to adult stages and specifically expressed in oocytes and spermatogonia. During embryonic development, Duxbl is transcribed in limbs and tail. However, Duxbl proteins were only detected in trunk and limb muscles and in elongated myocytes and myotubes. In C2C12 muscle cell line, Duxbl expression pattern is similar to differentiated marker gene, Myogenin, increased in expression from 2 days onward in differentiating medium. We suggest that Duxbl proteins play regulatory roles during myogenesis and reproductive developments. Copyright (c) 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20063414     DOI: 10.1002/dvdy.22210

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  17 in total

Review 1.  Facioscapulohumeral muscular dystrophy and DUX4: breaking the silence.

Authors:  Silvère M van der Maarel; Rabi Tawil; Stephen J Tapscott
Journal:  Trends Mol Med       Date:  2011-02-01       Impact factor: 11.951

2.  Evolution of DUX gene macrosatellites in placental mammals.

Authors:  Andreas Leidenroth; Jannine Clapp; Laura M Mitchell; Daniel Coneyworth; Frances L Dearden; Leopoldo Iannuzzi; Jane E Hewitt
Journal:  Chromosoma       Date:  2012-08-18       Impact factor: 4.316

3.  DUX4 activates germline genes, retroelements, and immune mediators: implications for facioscapulohumeral dystrophy.

Authors:  Linda N Geng; Zizhen Yao; Lauren Snider; Abraham P Fong; Jennifer N Cech; Janet M Young; Silvere M van der Maarel; Walter L Ruzzo; Robert C Gentleman; Rabi Tawil; Stephen J Tapscott
Journal:  Dev Cell       Date:  2011-12-29       Impact factor: 12.270

4.  Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model.

Authors:  Jessica C de Greef; Yvonne D Krom; Bianca den Hamer; Lauren Snider; Yosuke Hiramuki; Rob F P van den Akker; Kelsey Breslin; Miha Pakusch; Daniela C F Salvatori; Bram Slütter; Rabi Tawil; Marnie E Blewitt; Stephen J Tapscott; Silvère M van der Maarel
Journal:  Hum Mol Genet       Date:  2018-02-15       Impact factor: 6.150

Review 5.  Deciphering transcription dysregulation in FSH muscular dystrophy.

Authors:  Melanie Ehrlich; Michelle Lacey
Journal:  J Hum Genet       Date:  2012-06-21       Impact factor: 3.172

6.  Testing the effects of FSHD candidate gene expression in vertebrate muscle development.

Authors:  Ryan D Wuebbles; Steven W Long; Meredith L Hanel; Peter L Jones
Journal:  Int J Clin Exp Pathol       Date:  2010-03-28

7.  Dominant lethal pathologies in male mice engineered to contain an X-linked DUX4 transgene.

Authors:  Abhijit Dandapat; Darko Bosnakovski; Lynn M Hartweck; Robert W Arpke; Kristen A Baltgalvis; Derek Vang; June Baik; Radbod Darabi; Rita C R Perlingeiro; F Kent Hamra; Kalpna Gupta; Dawn A Lowe; Michael Kyba
Journal:  Cell Rep       Date:  2014-08-28       Impact factor: 9.423

Review 8.  Current Therapeutic Approaches in FSHD.

Authors:  Leo H Wang; Rabi Tawil
Journal:  J Neuromuscul Dis       Date:  2021

9.  A family history of DUX4: phylogenetic analysis of DUXA, B, C and Duxbl reveals the ancestral DUX gene.

Authors:  Andreas Leidenroth; Jane E Hewitt
Journal:  BMC Evol Biol       Date:  2010-11-26       Impact factor: 3.260

10.  Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene.

Authors:  Lauren Snider; Linda N Geng; Richard J L F Lemmers; Michael Kyba; Carol B Ware; Angelique M Nelson; Rabi Tawil; Galina N Filippova; Silvère M van der Maarel; Stephen J Tapscott; Daniel G Miller
Journal:  PLoS Genet       Date:  2010-10-28       Impact factor: 5.917

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