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MyoD 的早期转录靶标将肌发生和体节发生联系起来。

Early transcriptional targets of MyoD link myogenesis and somitogenesis.

机构信息

Biology Department, University of York, Heslington, York, North Yorkshire YO10 5YW, UK.

出版信息

Dev Biol. 2012 Nov 15;371(2):256-68. doi: 10.1016/j.ydbio.2012.08.027. Epub 2012 Aug 31.

Abstract

In order to identify early transcriptional targets of MyoD prior to skeletal muscle differentiation, we have undertaken a transcriptomic analysis on gastrula stage Xenopus embryos in which MyoD has been knocked-down. Our validated list of genes transcriptionally regulated by MyoD includes Esr1 and Esr2, which are known targets of Notch signalling, and Tbx6, mesogenin, and FoxC1; these genes are all are known to be essential for normal somitogenesis but are expressed surprisingly early in the mesoderm. In addition we found that MyoD is required for the expression of myf5 in the early mesoderm, in contrast to the reverse relationship of these two regulators in amniote somites. These data highlight a role for MyoD in the early mesoderm in regulating a set of genes that are essential for both myogenesis and somitogenesis.

摘要

为了在骨骼肌分化之前鉴定 MyoD 的早期转录靶标,我们对 MyoD 被敲低的原肠胚期 Xenopus 胚胎进行了转录组分析。我们验证的 MyoD 转录调控基因列表包括已知的 Notch 信号通路靶标 Esr1 和 Esr2,以及 Tbx6、Mesogenin 和 FoxC1;这些基因对于正常体节形成都是必需的,但在中胚层中表达得非常早。此外,我们发现 MyoD 对于早期中胚层中 myf5 的表达是必需的,这与这两个在羊膜动物体节中的调节因子的相反关系形成对比。这些数据突出了 MyoD 在早期中胚层中调节一组对于肌发生和体节形成都是必需的基因的作用。

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