Literature DB >> 15302601

Tbx5 and Tbx4 transcription factors interact with a new chicken PDZ-LIM protein in limb and heart development.

Ange Krause1, William Zacharias, Troy Camarata, Barbara Linkhart, Evelyn Law, Antje Lischke, Erik Miljan, Hans-Georg Simon.   

Abstract

The T-domain transcription factors, Tbx5 and Tbx4, play important roles in vertebrate limb and heart development. To identify interacting and potential Tbx-regulating proteins, we performed a yeast two-hybrid screen with the C-terminal domain of Tbx5 as bait. We identified a new PDZ-LIM protein composed of one N-terminal PDZ and three C-terminal LIM domains, which we named chicken LMP-4. Among the Tbx2, 3, 4, 5 subfamily, we observed exclusive interaction with Tbx5 and Tbx4 proteins. Tbx3 nor Tbx2 can substitute for LMP-4 binding. While chicken LMP-4 associates with Tbx5 or Tbx4, it uses distinct LIM domains to bind to the individual proteins. Subcellular co-localization of LMP-4 and Tbx proteins supports the protein interaction and reveals interference of LMP-4 with Tbx protein distribution, tethering the transcription factors to the cytoskeleton. The protein-protein interaction indicates regulation of Tbx function at the level of transcription factor nuclear localization. During chicken limb and heart development, Tbx5/LMP-4 and Tbx4/LMP-4 are tightly co-expressed in a temporal and spatial manner, suggesting that they operate in the same pathway. Surprisingly, chicken LMP-4 expression domains outside those of Tbx5 in the heart led to the discovery of Tbx4 expression in the outflow tract and the right ventricle of this organ. The Tbx4-expressing cells coincide with those of the recently discovered secondary anterior heart-forming field. The discrete posterior or anterior expression domains in the heart and the exclusive fore- or hindlimb expression of Tbx5 and Tbx4, respectively, suggest common pathways in the heart and limbs. The identification of a new Tbx5/4-specific binding factor further suggests a novel mechanism for Tbx transcription factor regulation in development and disease.

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Year:  2004        PMID: 15302601     DOI: 10.1016/j.ydbio.2004.05.024

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


  35 in total

1.  Identity and fate of Tbx4-expressing cells reveal developmental cell fate decisions in the allantois, limb, and external genitalia.

Authors:  L A Naiche; Ripla Arora; Artur Kania; Mark Lewandoski; Virginia E Papaioannou
Journal:  Dev Dyn       Date:  2011-10       Impact factor: 3.780

2.  Cloning and expression of a novel human gene, Isl-2, encoded a LIM-homeodomain protein.

Authors:  Yongqing Li; Yuejuan Zhang; Bei He; Yuequn Wang; Zengjin Yuan; Wuzhou Yuan; Peng Liao; Yun Deng; Jing Xiao; Chuanbing Zhu; Ying Wang; Xiushan Wu; Mingyao Liu
Journal:  Mol Biol Rep       Date:  2006-11-08       Impact factor: 2.316

3.  The protein ENH is a cytoplasmic sequestration factor for Id2 in normal and tumor cells from the nervous system.

Authors:  Anna Lasorella; Antonio Iavarone
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-20       Impact factor: 11.205

4.  An evolutionarily conserved nuclear export signal facilitates cytoplasmic localization of the Tbx5 transcription factor.

Authors:  Andre Kulisz; Hans-Georg Simon
Journal:  Mol Cell Biol       Date:  2007-12-26       Impact factor: 4.272

5.  Physical interaction between TBX5 and MEF2C is required for early heart development.

Authors:  Tushar K Ghosh; Fei Fei Song; Elizabeth A Packham; Sarah Buxton; Thelma E Robinson; Jonathan Ronksley; Tim Self; Andrew J Bonser; J David Brook
Journal:  Mol Cell Biol       Date:  2009-02-09       Impact factor: 4.272

6.  Tbx4/5 gene duplication and the origin of vertebrate paired appendages.

Authors:  Carolina Minguillon; Jeremy J Gibson-Brown; Malcolm P Logan
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-07       Impact factor: 11.205

7.  Differential regulation of Tbx5 protein expression and sub-cellular localization during heart development.

Authors:  Benjamin Bimber; Robert W Dettman; Hans-Georg Simon
Journal:  Dev Biol       Date:  2006-09-16       Impact factor: 3.582

Review 8.  T-box factors determine cardiac design.

Authors:  W M H Hoogaars; P Barnett; A F M Moorman; V M Christoffels
Journal:  Cell Mol Life Sci       Date:  2007-03       Impact factor: 9.261

9.  Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly.

Authors:  J A Rosenfeld; K H Kim; B Angle; R Troxell; J L Gorski; M Westemeyer; M Frydman; Y Senturias; D Earl; B Torchia; R A Schultz; J W Ellison; K Tsuchiya; S Zimmerman; T A Smolarek; B C Ballif; L G Shaffer
Journal:  Mol Syndromol       Date:  2013-01-05

10.  Splice variants of enigma homolog, differentially expressed during heart development, promote or prevent hypertrophy.

Authors:  Tomoko Yamazaki; Sébastien Wälchli; Toshitsugu Fujita; Stephan Ryser; Masahiko Hoshijima; Werner Schlegel; Shun'ichi Kuroda; Andrés D Maturana
Journal:  Cardiovasc Res       Date:  2010-01-22       Impact factor: 10.787

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