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在缺乏驱动蛋白KIF3B的小鼠中,由于节点纤毛缺失导致胚外液向左流动丧失,从而出现左右不对称随机化。

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein.

作者信息

Nonaka S, Tanaka Y, Okada Y, Takeda S, Harada A, Kanai Y, Kido M, Hirokawa N

机构信息

Department of Cell Biology and Anatomy, Graduate School of Medicine, University of Tokyo, Japan.

出版信息

Cell. 1998 Dec 11;95(6):829-37. doi: 10.1016/s0092-8674(00)81705-5.

Abstract

Microtubule-dependent motor, murine KIF3B, was disrupted by gene targeting. The null mutants did not survive beyond midgestation, exhibiting growth retardation, pericardial sac ballooning, and neural tube disorganization. Prominently, the left-right asymmetry was randomized in the heart loop and the direction of embryonic turning. lefty-2 expression was either bilateral or absent. Furthermore, the node lacked monocilia while the basal bodies were present. Immunocytochemistry revealed KIF3B localization in wild-type nodal cilia. Video microscopy showed that these cilia were motile and generated a leftward flow. These data suggest that KIF3B is essential for the left-right determination through intraciliary transportation of materials for ciliogenesis of motile primary cilia that could produce a gradient of putative morphogen along the left-right axis in the node.

摘要

微管依赖性马达蛋白小鼠KIF3B通过基因打靶被破坏。无效突变体在妊娠中期后无法存活,表现出生长迟缓、心包囊膨胀和神经管紊乱。显著的是,心脏环和胚胎旋转方向的左右不对称性被随机化。lefty-2表达要么是双侧的,要么不存在。此外,节点缺乏单纤毛,而基体存在。免疫细胞化学显示KIF3B定位于野生型节点纤毛中。视频显微镜显示这些纤毛是运动的,并产生向左的流动。这些数据表明,KIF3B对于通过为运动初级纤毛的纤毛发生进行材料的纤毛内运输来确定左右是必不可少的,这可以在节点中沿左右轴产生假定形态发生素的梯度。

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