Literature DB >> 19247927

The Xenopus Bowline/Ripply family proteins negatively regulate the transcriptional activity of T-box transcription factors.

Keisuke Hitachi1, Hiroki Danno, Shunsuke Tazumi, Yuko Aihara, Hideho Uchiyama, Koji Okabayashi, Akiko Kondow, Makoto Asashima.   

Abstract

Bowline, which is a member of the Xenopus Bowline/Ripply family of proteins, represses the transcription of somitogenesis-related genes before somite segmentation, which makes Bowline indispensable for somitogenesis. Although there are three bowline/Ripply family genes in each vertebrate species, it is not known whether the Bowline/Ripply family proteins share a common role in development. To elucidate their developmental roles, we examined the expression patterns and functions of the Xenopus Bowline/Ripply family proteins Bowline, Ledgerline, and a novel member of this protein family, xRipply3. We found that the expression patterns of bowline and ledgerline overlapped in the presomitic mesoderm (PSM), whereas ledgerline was additionally expressed in the newly formed somites. In addition, we isolated xRipply3, which is expressed in the pharyngeal region. Co-immunoprecipitation assays revealed that Ledgerline and xRipply3 interacted with T-box proteins and the transcriptional co-repressor Groucho/TLE. In luciferase assays, xRipply3 weakly suppressed the transcriptional activity of Tbx1, while Ledgerline strongly suppressed that of Tbx6. In line with the repressive role of Ledgerline, knockdown of Ledgerline resulted in enlargement of expression regions of the somitogenesis-related-genes mespb and Tbx6. Inhibition of histone deacetylase activity increased the expression of mespb, as seen in the Bowline and Ledgerline knockdown experiments. These results suggest that the Groucho-HDAC complex is required for the repressive activity of Bowline/Ripply family proteins during Xenopus somitogenesis. We conclude that although the Xenopus Bowline/Ripply family proteins Bowline, Ledgerline and xRipply3 are expressed differentially, they all act as negative regulators of T-box proteins.

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Year:  2009        PMID: 19247927     DOI: 10.1387/ijdb.082823kh

Source DB:  PubMed          Journal:  Int J Dev Biol        ISSN: 0214-6282            Impact factor:   2.203


  11 in total

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Journal:  Development       Date:  2012-03       Impact factor: 6.868

2.  The retinoblastoma protein modulates Tbx2 functional specificity.

Authors:  Keith W Vance; Heather M Shaw; Mercedes Rodriguez; Sascha Ott; Colin R Goding
Journal:  Mol Biol Cell       Date:  2010-06-09       Impact factor: 4.138

3.  Function of the C. elegans T-box factor TBX-2 depends on interaction with the UNC-37/Groucho corepressor.

Authors:  Paul Huber; Tanya Crum; Peter G Okkema
Journal:  Dev Biol       Date:  2016-06-02       Impact factor: 3.582

4.  Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome.

Authors:  Ender Karaca; Ozge O Yuregir; Sevcan T Bozdogan; Huseyin Aslan; Davut Pehlivan; Shalini N Jhangiani; Zeynep C Akdemir; Tomasz Gambin; Yavuz Bayram; Mehmed M Atik; Serkan Erdin; Donna Muzny; Richard A Gibbs; James R Lupski
Journal:  Am J Med Genet A       Date:  2015-08-04       Impact factor: 2.802

5.  The Caenorhabditis elegans T-box factor MLS-1 requires Groucho co-repressor interaction for uterine muscle specification.

Authors:  Raymond R Miller; Peter G Okkema
Journal:  PLoS Genet       Date:  2011-08-11       Impact factor: 5.917

6.  In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency.

Authors:  George E Gentsch; Nick D L Owens; Stephen R Martin; Paul Piccinelli; Tiago Faial; Matthew W B Trotter; Michael J Gilchrist; James C Smith
Journal:  Cell Rep       Date:  2013-09-19       Impact factor: 9.423

7.  Tbx protein level critical for clock-mediated somite positioning is regulated through interaction between Tbx and Ripply.

Authors:  Chimwar Wanglar; Jun Takahashi; Taijiro Yabe; Shinji Takada
Journal:  PLoS One       Date:  2014-09-26       Impact factor: 3.240

8.  Putative Breast Cancer Driver Mutations in TBX3 Cause Impaired Transcriptional Repression.

Authors:  Kathrin Fischer; Gert O Pflugfelder
Journal:  Front Oncol       Date:  2015-10-29       Impact factor: 6.244

9.  Insm1 promotes endocrine cell differentiation by modulating the expression of a network of genes that includes Neurog3 and Ripply3.

Authors:  Anna B Osipovich; Qiaoming Long; Elisabetta Manduchi; Rama Gangula; Susan B Hipkens; Judsen Schneider; Tadashi Okubo; Christian J Stoeckert; Shinji Takada; Mark A Magnuson
Journal:  Development       Date:  2014-08       Impact factor: 6.868

10.  Ripply2 recruits proteasome complex for Tbx6 degradation to define segment border during murine somitogenesis.

Authors:  Wei Zhao; Masayuki Oginuma; Rieko Ajima; Makoto Kiso; Akemi Okubo; Yumiko Saga
Journal:  Elife       Date:  2018-05-15       Impact factor: 8.140

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