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首页> 外文期刊>Stem cells and development >GATA factors lie upstream of Nkx 2.5 in the transcriptional regulatory cascade that effects cardiogenesis.
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GATA factors lie upstream of Nkx 2.5 in the transcriptional regulatory cascade that effects cardiogenesis.

机译:GATA因子位于影响心脏发生的转录调控级联反应中Nkx 2.5的上游。

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摘要

Members of the GATA-4, -5, and -6 subfamily of transcription factors are co-expressed with the homeoprotein Nkx 2.5 in the precardiac mesoderm during the earliest stages of its specification and are known to be important determinants of cardiac gene expression. Ample evidence suggests that GATA factors and Nkx 2.5 cross-regulate each other's expression; however, the temporal order of the expression of these transcription factors in vivo remains unresolved, and thus precise definition of the role of the products of the genes they transcribe in early development has been difficult to assess. We employed P19 CL6 mouse embryonic carcinoma cells as a model to investigate this problem, because these cells, like embryonic stem cells, can be induced to differentiate along multiple lineages. Here we demonstrate that when P19 CL6 cells are induced to differentiate to a cardiogenic lineage, the expression of GATA-4 and GATA-6 is up-regulated prior to the transcriptional activation of Nkx 2.5. Moreover, over-expression of GATA-4 or -6 at the time of Nkx 2.5 induction results in a significant up-regulation of endogenous Nkx 2.5 transcription. Finally, it is known that a Nkx-dependent enhancer is necessary for GATA-6 expression within cardiomyocytes of the developing mouse embryo. We demonstrate that within undifferentiated P19 CL6 cells, GATA-6 expression is subject to active repression by a novel upstream element that possesses binding sites for factors involved in transcriptional repression that are conserved between mammalian species.
机译:转录因子的GATA-4,-5和-6亚家族成员在规范化的最早阶段与心脏前中胚层中的同源蛋白Nkx 2.5共表达,并且已知是心脏基因表达的重要决定因素。大量证据表明,GATA因子和Nkx 2.5相互调节彼此的表达。然而,这些转录因子在体内表达的时间顺序仍未解决,因此很难评估它们转录的基因产物在早期发育中的作用的精确定义。我们使用P19 CL6小鼠胚胎癌细胞作为模型来研究此问题,因为这些细胞像胚胎干细胞一样可以被诱导沿多个谱系分化。在这里,我们证明当诱导P19 CL6细胞分化为心源性谱系时,在Nkx 2.5转录激活之前,GATA-4和GATA-6的表达被上调。此外,在Nkx 2.5诱导时GATA-4或-6的过表达导致内源性Nkx 2.5转录的显着上调。最后,已知在发育中的小鼠胚胎的心肌细胞内GATA-6表达需要Nkx依赖性增强子。我们证明,在未分化的P19 CL6细胞内,GATA-6表达受到新型上游元件的主动抑制,该上游元件具有与参与哺乳动物哺乳动物之间保守的转录抑制因子有关的结合位点。

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