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胚胎节点纤毛的保守功能。

Conserved function for embryonic nodal cilia.

作者信息

Essner Jeffrey J, Vogan Kyle J, Wagner Molly K, Tabin Clifford J, Yost H Joseph, Brueckner Martina

机构信息

Center for Children, Huntsman Cancer Institute and Department of Oncological Sciences, University of Utah, Salt Lake City, Utah 84112-5550, USA.

出版信息

Nature. 2002 Jul 4;418(6893):37-8. doi: 10.1038/418037a.

DOI:10.1038/418037a
PMID:12097899
Abstract

How left right handedness originates in the body plan of the developing vertebrate embryo is a subject of considerable debate. In mice, a left right bias is thought to arise from a directional extracellular flow (nodal flow) that is generated by dynein-dependent rotation of monocilia on the ventral surface of the embryonic node. Here we show that the existence of node monocilia and the expression of a dynein gene that is implicated in ciliary function are conserved across a wide range of vertebrate classes, indicating that a similar ciliary mechanism may underlie the establishment of handedness in all vertebrates.

摘要

在发育中的脊椎动物胚胎的身体结构中,左右利手性是如何起源的,这是一个备受争议的话题。在小鼠中,左右偏向被认为源于一种定向的细胞外流动(节点流),这种流动是由胚胎节点腹侧表面的单纤毛的动力蛋白依赖性旋转产生的。在这里,我们表明,节点单纤毛的存在以及与纤毛功能相关的动力蛋白基因的表达在广泛的脊椎动物类别中都是保守的,这表明类似的纤毛机制可能是所有脊椎动物中利手性建立的基础。

相似文献

1
Conserved function for embryonic nodal cilia.胚胎节点纤毛的保守功能。
Nature. 2002 Jul 4;418(6893):37-8. doi: 10.1038/418037a.
2
Embryology: fluid flow and broken symmetry.胚胎学:流体流动与对称性破缺
Nature. 2002 Jul 4;418(6893):29-30. doi: 10.1038/418029a.
3
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Nodal flow and the generation of left-right asymmetry.节点流与左右不对称性的产生
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PLoS One. 2010 Feb 2;5(2):e8999. doi: 10.1371/journal.pone.0008999.
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Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries.对左右动力蛋白的ATP结合结构域进行靶向缺失,证实了其在确定左右不对称发育中的作用。
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Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis.斑马鱼前肾、脑和库普弗小泡中由纤毛驱动的液体流动是正常器官发生所必需的。
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Targeted deletion of the novel cytoplasmic dynein mD2LIC disrupts the embryonic organiser, formation of the body axes and specification of ventral cell fates.新型细胞质动力蛋白mD2LIC的靶向缺失会破坏胚胎组织者、体轴形成以及腹侧细胞命运的特化。
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Dynamic forces drive cell and organ morphology changes during embryonic development.动态力在胚胎发育过程中驱动细胞和器官形态的变化。
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Novel compound heterozygous mutation in causes complex congenital heart disease.
[某种基因]中的新型复合杂合突变导致复杂先天性心脏病。 (注:原文中“in”后面缺少具体基因名称)
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Breaking Left-Right Symmetry by the Interplay of Planar Cell Polarity, Calcium Signaling and Cilia.通过平面细胞极性、钙信号传导和纤毛的相互作用打破左右对称性
Cells. 2024 Dec 20;13(24):2116. doi: 10.3390/cells13242116.
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Cdon is essential for organ left-right patterning by regulating dorsal forerunner cells clustering and Kupffer's vesicle morphogenesis.Cdon通过调节背侧先驱细胞聚集和库普弗小泡形态发生,对器官左右模式形成至关重要。
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