Plageman Timothy F, Yutzey Katherine E
Division of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.
J Biol Chem. 2004 Apr 30;279(18):19026-34. doi: 10.1074/jbc.M314041200. Epub 2004 Feb 20.
The T-box transcription factors play critical roles in embryonic development including cell type specification, tissue patterning, and morphogenesis. Several T-box genes are expressed in the heart and are regulators of cardiac development. At the earliest stages of heart development, two of these genes, Tbx5 and Tbx20, are co-expressed in the heart-forming region but then become differentially expressed as heart morphogenesis progresses. Although Tbx5 and Tbx20 belong to the same gene family and share a highly conserved DNA-binding domain, their transcriptional activities are distinct. The C-terminal region of the Tbx5 protein is a transcriptional activator, while the C terminus of Tbx20 can repress transcription. Tbx5, but not Tbx20, activates a cardiac-specific promoter (atrial natriuretic factor (ANF)) alone and synergistically with other transcription factors. In contrast, Tbx20 represses ANF promoter activity and also inhibits the activation mediated by Tbx5. Of the two T-box binding consensus sequences in the promoter of ANF, only T-box binding element 1 (TBE1) is required for the synergistic activation of ANF by Tbx5 and GATA4, but TBE2 is required for repression by Tbx20. To elucidate upstream signaling pathways that regulate Tbx5 and Tbx20 expression, recombinant bone morphogenetic protein-2 was added to cardiogenic explants from chick embryos. Using real time reverse transcription-PCR, it was demonstrated that Tbx20, but not Tbx5, is induced by bone morphogenetic protein-2. Collectively these data demonstrate clear differences in both the expression and function of two related transcription factors and suggest that the modulation of cardiac gene expression can occur as a result of combinatorial regulatory interactions of T-box proteins.
T-box转录因子在胚胎发育过程中发挥着关键作用,包括细胞类型的特化、组织模式形成和形态发生。几个T-box基因在心脏中表达,是心脏发育的调节因子。在心脏发育的最早阶段,其中两个基因Tbx5和Tbx20在心脏形成区域共同表达,但随着心脏形态发生的进展,它们随后会出现差异表达。尽管Tbx5和Tbx20属于同一基因家族并共享一个高度保守的DNA结合结构域,但它们的转录活性却截然不同。Tbx5蛋白的C末端区域是转录激活因子,而Tbx20的C末端则可抑制转录。Tbx5能单独激活心脏特异性启动子(心钠素(ANF)),并与其他转录因子协同激活,而Tbx20则不能。相反,Tbx20抑制ANF启动子活性,还能抑制Tbx5介导的激活作用。在ANF启动子中的两个T-box结合共有序列中,只有T-box结合元件1(TBE1)是Tbx5和GATA4协同激活ANF所必需的,但TBE2是Tbx20抑制作用所必需的。为了阐明调节Tbx5和Tbx20表达的上游信号通路,将重组骨形态发生蛋白-2添加到鸡胚的心脏原基外植体中。通过实时逆转录-聚合酶链反应表明,骨形态发生蛋白-2可诱导Tbx20表达,而不能诱导Tbx5表达。这些数据共同表明了两个相关转录因子在表达和功能上的明显差异,并提示心脏基因表达的调控可能是T-box蛋白组合调控相互作用的结果。