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CDC-42调节PAR蛋白的定位和功能,以控制秀丽隐杆线虫中的细胞极性和胚胎极性。

CDC-42 regulates PAR protein localization and function to control cellular and embryonic polarity in C. elegans.

作者信息

Kay A J, Hunter C P

机构信息

Department of Molecular and Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA.

出版信息

Curr Biol. 2001 Apr 3;11(7):474-81. doi: 10.1016/s0960-9822(01)00141-5.

Abstract

BACKGROUND

The polarization of the anterior-posterior axis (A-P) of the Caenorhabditis elegans zygote depends on the activity of the par genes and the presence of intact microfilaments. Functional links between the PAR proteins and the cytoskeleton, however, have not been fully explored. It has recently been shown that in mammalian cells, some PAR homologs form a complex with activated Cdc42, a Rho GTPase that is implicated in the control of actin organization and cellular polarity. A role for Cdc42 in the establishment of embryonic polarity in C. elegans has not been described.

RESULTS

To investigate the function of Cdc42 in the control of cellular and embryonic polarity in C. elegans, we used RNA-mediated interference (RNAi) to inhibit cdc-42 activity in the early embryo. Here, we demonstrate that RNAi of cdc-42 disrupts manifestations of polarity in the early embryo, that these phenotypes depend on par-2 and par-3 gene function, and that cdc-42 is required for the localization of the PAR proteins.

CONCLUSIONS

Our genetic analysis of the regulatory relationships between cdc-42 and the par genes demonstrates that Cdc42 organizes embryonic polarity by controlling the localization and activity of the PAR proteins. Combined with the recent biochemical analysis of their mammalian homologs, these results simultaneously identify both a regulator of the PAR proteins, activated Cdc42, and effectors for Cdc42, the PAR complex.

摘要

背景

秀丽隐杆线虫受精卵前后轴(A-P)的极化取决于par基因的活性和完整微丝的存在。然而,PAR蛋白与细胞骨架之间的功能联系尚未得到充分探索。最近研究表明,在哺乳动物细胞中,一些PAR同源物与活化的Cdc42形成复合物,Cdc42是一种Rho GTP酶,与肌动蛋白组织和细胞极性的控制有关。尚未有关于Cdc42在秀丽隐杆线虫胚胎极性建立中作用的描述。

结果

为了研究Cdc42在秀丽隐杆线虫细胞和胚胎极性控制中的功能,我们使用RNA介导的干扰(RNAi)来抑制早期胚胎中cdc-42的活性。在此,我们证明cdc-42的RNAi破坏了早期胚胎中的极性表现,这些表型取决于par-2和par-3基因的功能,并且cdc-42是PAR蛋白定位所必需的。

结论

我们对cdc-42与par基因之间调控关系的遗传分析表明,Cdc42通过控制PAR蛋白的定位和活性来组织胚胎极性。结合最近对其哺乳动物同源物的生化分析,这些结果同时确定了PAR蛋白的一个调节因子,即活化的Cdc42,以及Cdc42的效应器,即PAR复合物。

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