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首页> 外文期刊>Journal of Muscle Research and Cell Motility >Six and Eya expression during human somitogenesis and MyoD gene family activation
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Six and Eya expression during human somitogenesis and MyoD gene family activation

机译:人的体发生和MyoD基因家族激活过程中的六和Eya表达

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This report describes the characterisation of the expression profile of several myogenic determination genes during human embryogenesis. The data were obtained from axial structures and limb buds of human embryos aged between 3 and 8 weeks of development. Using in situ hybridisation to detect Pax3 and MyoD gene family mRNAs, and immunochemistry to follow Six and Eya protein accumulation, we have been able to establish the chronology of accumulation of these gene products. As in mouse, the first transcripts detected in myotomes of 3 week-old embryos are Pax3 and Myf5, followed by the expression of myogenin. MyoD appears to be activated well after Myf5, myogenin and MRF4 in the early myotome, whereas, in limb bud muscles, the presence of all four of these mRNAs is concomitant from 6 weeks. Six1, Six4 and Six5 homeoproteins are detected later than Myf5 activation. These Six homeoproteins are first observed in the cytoplasm of myogenin expressing cells. At later stages of development, Six1 and Six5, but not Six4, are translocated into the nuclei of myogenic cells, concomitantly with MyHCemb expression. Eya1 and Eya2 proteins, potential Six cofactors, were also detected in myogenin positive cells, but their accumulation was delayed and was mainly cytoplasmic. These results preclude that early activation of Myf5, myogenin and MRF4 is under the control of Six and Eya proteins, while Six and Eya proteins would be involved in later steps of myogenic differentiation.
机译:这份报告描述了人类胚胎发生过程中几个生肌测定基因表达谱的表征。这些数据是从发育3至8周的人类胚胎的轴结构和肢芽中获得的。使用原位杂交检测Pax3和MyoD基因家族的mRNA,并使用免疫化学方法追踪6和Eya蛋白的积累,我们已经能够确定这些基因产物积累的时间顺序。与小鼠一样,在3周大的胚胎的肌组织中检测到的第一个转录物是Pax3和Myf5,然后是肌生成素的表达。 MyoD似乎在Myf5,Myogenin和MRF4在早期的子宫肌瘤中被很好地激活,而在肢芽肌肉中,从6周开始,所有这四个mRNA的出现都伴随着。在Myf5激活之后,检测到Six1,Six4和Six5同源蛋白。这六种同源蛋白首先在表达肌成蛋白的细胞的细胞质中观察到。在发育的后期,Six1和Six5(而不是Six4)被转移到成肌细胞的核中,并伴随着MyHCemb的表达。 Eya1和Eya2蛋白,潜在的六种辅助因子,在肌生成素阳性细胞中也被检测到,但它们的积累被延迟并且主要是胞质的。这些结果排除了Myf5,myogenin和MRF4的早期活化受Six和Eya蛋白的控制,而Six和Eya蛋白将参与成肌分化的后续步骤。

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