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Serum response factor micromanaging cardiogenesis.

机译:血清反应因子微观管理心脏发生。

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摘要

Serum response factor (SRF), a cardiac-enriched transcription factor, is required for the appearance of beating sarcomeres in the heart. SRF may also direct the expression of microRNAs (miRs) that inhibit the expression of cardiac regulatory factors. The recent knockout of miR-1-2, an SRF gene target, showed defective heart development, caused in part by the induction of GATA6, Irx4/5, and Hand2, that may alter cardiac morphogenesis, channel activity, and cell cycling. SRF and cofactors play an obligatory role in cardiogenesis, as major determinants of myocyte differentiation not only by regulating the biogenesis of muscle contractile proteins but also by driving the expression of silencer miRNA.
机译:心脏搏动性肉瘤的出现需要血清反应因子(SRF)(一种富含心脏的转录因子)。 SRF还可以指导抑制心脏调节因子表达的microRNA(miR)的表达。最近敲除的SRF基因靶标miR-1-2,显示出心脏发育不良,部分是由GATA6,Irx4 / 5和Hand2的诱导引起的,这可能会改变心脏的形态,通道活性和细胞周期。 SRF和辅因子在心肌发生中起着必不可少的作用,它不仅是调节肌肉收缩蛋白的生物发生,而且还通过驱动沉默子miRNA的表达,成为心肌细胞分化的主要决定因素。

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