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海鞘胚胎中肌肉细胞自主分化的内在遗传程序。

An intrinsic genetic program for autonomous differentiation of muscle cells in the ascidian embryo.

作者信息

Satoh N, Araki I, Satou Y

机构信息

Department of Zoology, Graduate School of Science, Kyoto University, Japan.

出版信息

Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9315-21. doi: 10.1073/pnas.93.18.9315.

DOI:10.1073/pnas.93.18.9315
PMID:8790327
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC38425/
Abstract

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.

摘要

海鞘胚胎的B线推定肌细胞具有广泛的自我分化潜能,这种潜能依赖于受精卵肌质中预先定位的决定因素。因此,海鞘幼虫肌细胞提供了一个实验系统,用以探索胚胎细胞自主特化的内在遗传程序。对卵片段的实验表明,母体mRNA是肌肉决定因素的组成部分之一。幼虫肌动蛋白基因的表达早在32细胞阶段就开始了,早于细胞发育命运的限制。肌动蛋白基因表达开始的时间比脊椎动物MyoD的海鞘同源物的表达提前几个小时。肌动蛋白基因5'侧翼区域近端E盒中的突变并未改变报告基因肌肉特异性表达的启动子活性。这些结果,连同融合基因缺失构建体的结果,表明肌肉决定因素直接或通过MyoD以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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed9/38425/4e61a3a863bf/pnas01522-0029-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed9/38425/8442ab4c9a33/pnas01522-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed9/38425/f4e3988b5afa/pnas01522-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed9/38425/4e61a3a863bf/pnas01522-0029-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed9/38425/8442ab4c9a33/pnas01522-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed9/38425/f4e3988b5afa/pnas01522-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed9/38425/4e61a3a863bf/pnas01522-0029-a.jpg

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本文引用的文献

1
Muscle deficiency and neonatal death in mice with a targeted mutation in the myogenin gene.肌细胞生成素基因靶向突变小鼠的肌肉缺陷与新生儿死亡
Nature. 1993 Aug 5;364(6437):501-6. doi: 10.1038/364501a0.
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Evolution of the chordate muscle actin gene.脊索动物肌肉肌动蛋白基因的进化。
J Mol Evol. 1993 Apr;36(4):361-8. doi: 10.1007/BF00182183.
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Short upstream sequences associated with the muscle-specific expression of an actin gene in ascidian embryos.与海鞘胚胎中肌动蛋白基因的肌肉特异性表达相关的短上游序列。
Dev Biol. 1994 Dec;166(2):763-9. doi: 10.1006/dbio.1994.1354.
8
Coexpression and promoter function in two muscle actin gene complexes of different structural organization in the ascidian Halocynthia roretzi.海鞘(Halocynthia roretzi)中不同结构组织的两种肌肉肌动蛋白基因复合体的共表达及启动子功能
Dev Biol. 1995 Jun;169(2):461-72. doi: 10.1006/dbio.1995.1161.
9
Myogenin's functions do not overlap with those of MyoD or Myf-5 during mouse embryogenesis.在小鼠胚胎发育过程中,肌细胞生成素的功能与肌分化抗原或肌因子5的功能并不重叠。
Dev Biol. 1995 Nov;172(1):37-50. doi: 10.1006/dbio.1995.0004.
10
Chordate muscle actins differ distinctly from invertebrate muscle actins. The evolution of the different vertebrate muscle actins.脊索动物的肌肉肌动蛋白与无脊椎动物的肌肉肌动蛋白明显不同。不同脊椎动物肌肉肌动蛋白的进化。
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