首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >An intrinsic genetic program for autonomous differentiation of muscle cells in the ascidian embryo.
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An intrinsic genetic program for autonomous differentiation of muscle cells in the ascidian embryo.

机译:一个固有的遗传程序可以自动分化海鞘胚胎中的肌肉细胞。

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摘要

The B-line presumptive muscle cells of ascidian embryos have extensive potential for self-differentiation dependent on determinants prelocalized in the myoplasm of fertilized eggs. Ascidian larval muscle cells therefore provide an experimental system with which to explore an intrinsic genetic program for autonomous specification of embryonic cells. Experiments with egg fragments suggested that maternal mRNAs are one of the components of muscle determinants. Expression of larval muscle actin genes begins as early as the 32-cell stage, prior to the developmental fate restriction of the cells. The timing of initiation of the actin gene expression proceeds the expression of an ascidian homologue of vertebrate MyoD by a few hours. Mutations in the proximal E-box of the 5' flanking region of the actin genes did not alter the promoter activity for muscle-specific expression of reporter gene. These results, together with results of deletion constructs of fusion genes, suggest that muscle determinants regulate directly, or indirectly via regulatory factors other than MyoD, the transcription of muscle-specific structural genes leading to the terminal differentiation.
机译:海鞘胚胎的B线推测性肌肉细胞具有广泛的自我分化潜能,具体取决于受精卵肌质中预先定位的决定簇。因此,海鞘幼虫肌肉细胞提供了一个实验系统,可利用该系统探索内在的遗传程序,以自动确定胚胎细胞。卵片段的实验表明,母体mRNA是肌肉决定簇的组成部分之一。幼虫肌肌动蛋白基因的表达最早在32细胞阶段开始,然后才是细胞的发育命运限制。肌动蛋白基因表达的起始时间使脊椎动物MyoD的海鞘同源物的表达进行数小时。肌动蛋白基因5'侧翼区的近端E盒中的突变不会改变报告基因的肌肉特异性表达的启动子活性。这些结果以及融合基因的缺失构建体的结果表明,肌肉决定簇直接或间接通过除MyoD之外的调节因子间接调节导致终末分化的肌肉特异性结构基因的转录。

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