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本文引用的文献

1
Timing of initiation of muscle-specific gene expression in the ascidian embryo precedes that of developmental fate restriction in lineage cells.海鞘胚胎中肌肉特异性基因表达开始的时间早于谱系细胞中发育命运限制的时间。
Dev Growth Differ. 1995 Jun;37(3):319-327. doi: 10.1046/j.1440-169X.1995.t01-2-00010.x.
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Genome-wide network of regulatory genes for construction of a chordate embryo.用于构建脊索动物胚胎的调控基因全基因组网络。
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3
Brachyury-downstream gene sets in a chordate, Ciona intestinalis: integrating notochord specification, morphogenesis and chordate evolution.尾索动物海鞘中短尾相关下游基因集:整合脊索的特化、形态发生与脊索动物进化
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Chongmague reveals an essential role for laminin-mediated boundary formation in chordate convergence and extension movements.崇马格揭示了层粘连蛋白介导的边界形成在脊索动物汇聚延伸运动中的重要作用。
Development. 2008 Jan;135(1):33-41. doi: 10.1242/dev.010892. Epub 2007 Nov 21.
5
Culture of Ciona intestinalis in closed systems.在封闭系统中培养玻璃海鞘。
Dev Dyn. 2007 Jul;236(7):1832-40. doi: 10.1002/dvdy.21124.
6
Overlapping expression of FoxA and Zic confers responsiveness to FGF signaling to specify notochord in ascidian embryos.FoxA和Zic的重叠表达赋予对FGF信号的反应能力,从而在海鞘胚胎中指定脊索。
Dev Biol. 2006 Dec 15;300(2):770-84. doi: 10.1016/j.ydbio.2006.07.033. Epub 2006 Aug 4.
7
Regulatory blueprint for a chordate embryo.脊索动物胚胎的调控蓝图。
Science. 2006 May 26;312(5777):1183-7. doi: 10.1126/science.1123404.
8
Microarray analysis of localization of maternal transcripts in eggs and early embryos of the ascidian, Ciona intestinalis.海鞘(Ciona intestinalis)卵和早期胚胎中母体转录本定位的微阵列分析。
Dev Biol. 2005 Aug 15;284(2):536-50. doi: 10.1016/j.ydbio.2005.05.027.
9
Specification of embryonic axis and mosaic development in ascidians.海鞘胚胎轴的特化与镶嵌发育
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10
Culture of adult ascidians and ascidian genetics.成体海鞘的培养与海鞘遗传学
Methods Cell Biol. 2004;74:143-70. doi: 10.1016/s0091-679x(04)74007-8.

短尾(Brachyury)基因敲除突变体诱导的幼体海鞘内胚层器官缺陷。

Brachyury null mutant-induced defects in juvenile ascidian endodermal organs.

作者信息

Chiba Shota, Jiang Di, Satoh Noriyuki, Smith William C

机构信息

Department of Molecular, Cell and Developmental Biology, University of California Santa Barbara, Santa Barbara, CA 93106, USA.

出版信息

Development. 2009 Jan;136(1):35-9. doi: 10.1242/dev.030981. Epub 2008 Nov 19.

DOI:10.1242/dev.030981
PMID:19019990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2685961/
Abstract

We report the isolation of a recessive ENU-induced short-tailed mutant in the ascidian Ciona intestinalis that is the product of a premature stop in the brachyury gene. Notochord differentiation and morphogenesis are severely disrupted in the mutant line. At the larval stage, variable degrees of ectopic endoderm staining were observed in the homozygous mutants, indicating that loss of brachyury results in stochastic fate transformation. In post-metamorphosis mutants, a uniform defect in tail resorption was observed, together with variable defects in digestive tract development. Some cells misdirected from the notochord lineage were found to be incorporated into definitive endodermal structures, such as stomach and intestine.

摘要

我们报告了在海鞘Ciona intestinalis中分离出一种隐性ENU诱导的短尾突变体,它是短尾基因中过早出现终止密码子的产物。在突变系中,脊索分化和形态发生受到严重破坏。在幼虫阶段,在纯合突变体中观察到不同程度的异位内胚层染色,这表明短尾基因的缺失导致了随机的命运转变。在变态后的突变体中,观察到尾部吸收存在一致的缺陷,同时消化道发育也存在不同程度的缺陷。一些从脊索谱系中错误定向的细胞被发现整合到了确定的内胚层结构中,如胃和肠。