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Tbx5和Tbx20协同作用以控制脊椎动物心脏形态发生。

Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis.

作者信息

Brown Daniel D, Martz Shauna N, Binder Olav, Goetz Sarah C, Price Brenda M J, Smith Jim C, Conlon Frank L

机构信息

Department of Genetics, Fordham Hall, UNC-Chapel Hill, Chapel Hill, NC 27599-3280, USA.

出版信息

Development. 2005 Feb;132(3):553-63. doi: 10.1242/dev.01596. Epub 2005 Jan 5.

Abstract

Members of the T-box family of proteins play a fundamental role in patterning the developing vertebrate heart; however, the precise cellular requirements for any one family member and the mechanism by which individual T-box genes function remains largely unknown. In this study, we have investigated the cellular and molecular relationship between two T-box genes, Tbx5 and Tbx20. We demonstrate that blocking Tbx5 or Tbx20 produces phenotypes that display a high degree of similarity, as judged by overall gross morphology, molecular marker analysis and cardiac physiology, implying that the two genes are required for and have non-redundant functions in early heart development. In addition, we demonstrate that although co-expressed, Tbx5 and Tbx20 are not dependent on the expression of one another, but rather have a synergistic role during early heart development. Consistent with this proposal, we show that TBX5 and TBX20 can physically interact and map the interaction domains, and we show a cellular interaction for the two proteins in cardiac development, thus providing the first evidence for direct interaction between members of the T-box gene family.

摘要

T-box蛋白家族成员在脊椎动物心脏发育的模式形成中发挥着重要作用;然而,对于任何一个家族成员的精确细胞需求以及单个T-box基因发挥作用的机制,在很大程度上仍然未知。在本研究中,我们调查了两个T-box基因Tbx5和Tbx20之间的细胞和分子关系。我们证明,通过整体大体形态、分子标记分析和心脏生理学判断,阻断Tbx5或Tbx20会产生高度相似的表型,这意味着这两个基因在早期心脏发育中是必需的且具有非冗余功能。此外,我们证明,尽管Tbx5和Tbx20共同表达,但它们并不相互依赖表达,而是在早期心脏发育过程中具有协同作用。与此提议一致,我们表明TBX5和TBX20可以发生物理相互作用并绘制相互作用结构域,并且我们展示了这两种蛋白质在心脏发育中的细胞相互作用,从而为T-box基因家族成员之间的直接相互作用提供了首个证据。

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