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在影响心脏发生的转录调控级联反应中,GATA因子位于Nkx 2.5的上游。

GATA factors lie upstream of Nkx 2.5 in the transcriptional regulatory cascade that effects cardiogenesis.

作者信息

Brewer Alison C, Alexandrovich Alexander, Mjaatvedt Corey H, Shah Ajay M, Patient Roger K, Pizzey John A

机构信息

Department of Cardiology, King's College Hospital, London SE5 9RS, UK.

出版信息

Stem Cells Dev. 2005 Aug;14(4):425-39. doi: 10.1089/scd.2005.14.425.

Abstract

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.

摘要

转录因子GATA-4、-5和-6亚家族的成员在心脏中胚层特化的最早阶段与同源结构域蛋白Nkx 2.5共同表达,并且已知它们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相互交叉调节彼此的表达;然而,这些转录因子在体内表达的时间顺序仍未明确,因此难以评估它们转录的基因产物在早期发育中的作用的确切定义。我们采用P19 CL6小鼠胚胎癌细胞作为模型来研究这个问题,因为这些细胞与胚胎干细胞一样,可以被诱导沿着多个谱系分化。在此我们证明,当P19 CL6细胞被诱导分化为心脏谱系时,GATA-4和GATA-6的表达在Nkx 2.5转录激活之前就上调了。此外,在诱导Nkx 2.5时过表达GATA-4或-6会导致内源性Nkx 2.5转录显著上调。最后,已知一个Nkx依赖性增强子对于发育中的小鼠胚胎心肌细胞内的GATA-6表达是必需的。我们证明,在未分化的P19 CL6细胞中,GATA-6的表达受到一个新的上游元件的主动抑制,该元件具有哺乳动物物种间保守的转录抑制相关因子的结合位点。

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