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VAB-8、UNC-73和MIG-2调节秀丽隐杆线虫中UNC-40的轴突极性和细胞迁移功能。

VAB-8, UNC-73 and MIG-2 regulate axon polarity and cell migration functions of UNC-40 in C. elegans.

作者信息

Levy-Strumpf Naomi, Culotti Joseph G

机构信息

Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Toronto, Ontario M5G 1X5, Canada.

出版信息

Nat Neurosci. 2007 Feb;10(2):161-8. doi: 10.1038/nn1835. Epub 2007 Jan 21.

Abstract

One of the most intriguing features of axons is their ability to pioneer precise paths to their targets. How guidance-cue information is interpreted and integrated to form intricate neuronal networks has not been fully deciphered. Using Caenorhabditis elegans, we show that highly conserved receptors that guide pioneer axons along the dorsoventral axis, such as UNC-40 and SAX-3 (receptors for UNC-6 and SLT-1 guidance cues, respectively), can be co-opted to affect axon and cell migrations along the anterior-posterior axis. We further identify the kinesin-related VAB-8 protein as an upstream regulator of UNC-40, illuminating VAB-8's mechanism of action in determining the polarity of cell and axon migration. Finally, we show that UNC-73 and its target MIG-2 function with VAB-8 as upstream regulators of UNC-40 and that MIG-2 activity specifies UNC-40 subcellular localization. These data are indicative of previously unidentified regulatory roles for VAB-8 and small GTPases, which act together to regulate guidance receptor functions.

摘要

轴突最引人入胜的特征之一是它们能够开辟精确的路径到达其靶标。引导线索信息是如何被解读和整合以形成复杂的神经网络,目前尚未完全弄清楚。利用秀丽隐杆线虫,我们发现,沿背腹轴引导先驱轴突的高度保守的受体,如UNC-40和SAX-3(分别是UNC-6和SLT-1引导线索的受体),可以被用于影响沿前后轴的轴突和细胞迁移。我们进一步确定了与驱动蛋白相关的VAB-8蛋白是UNC-40的上游调节因子,阐明了VAB-8在决定细胞和轴突迁移极性方面的作用机制。最后,我们表明UNC-73及其靶标MIG-2作为UNC-40的上游调节因子与VAB-8共同发挥作用,并且MIG-2的活性决定了UNC-40的亚细胞定位。这些数据表明VAB-8和小GTP酶具有以前未被识别的调节作用,它们共同作用来调节引导受体的功能。

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