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18轮大货车通过Rho-GTPase信号通路调节唾液腺细胞的顶端收缩。

18 wheeler regulates apical constriction of salivary gland cells via the Rho-GTPase-signaling pathway.

作者信息

Kolesnikov Tereza, Beckendorf Steven K

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.

出版信息

Dev Biol. 2007 Jul 1;307(1):53-61. doi: 10.1016/j.ydbio.2007.04.014. Epub 2007 Apr 20.

Abstract

Rho GTPase and its upstream activator, guanine nucleotide exchange factor 2 (RhoGEF2), have emerged as key regulators of actin rearrangements during epithelial folding and invagination (Nikolaidou, K.K., Barrett, K. (2004). A Rho-GTPase-signaling pathway is used reiteratively in epithelial folding and potentially selects the outcome of Rho activation. Curr. Biol. 14, 1822-1826). Here, we show that Drosophila 18 wheeler (18W), a Toll-like receptor protein, is a novel component of the Rho-signaling pathway involved in epithelial morphogenesis. 18w Mutant embryos have salivary gland invagination defects similar to embryos that lack components of the Rho pathway, and ubiquitous expression of 18W results in an upregulation of Rho signaling. Transheterozygous genetic interactions and double mutant analysis suggest that 18W affects the Rho-GTPase-signaling pathway not through Fog and RhoGEF2, but rather by inhibiting Rho GTPase activating proteins (RhoGAPs). We show that RhoGAP5A and RhoGAP88C/Crossveinless-c (CV-C) are required for proper salivary gland morphogenesis, implicating them as potential targets of 18W.

摘要

Rho GTP酶及其上游激活剂鸟嘌呤核苷酸交换因子2(RhoGEF2),已成为上皮细胞折叠和内陷过程中肌动蛋白重排的关键调节因子(Nikolaidou, K.K., Barrett, K. (2004). A Rho-GTPase-signaling pathway is used reiteratively in epithelial folding and potentially selects the outcome of Rho activation. Curr. Biol. 14, 1822-1826)。在此,我们表明果蝇18轮车(18W),一种Toll样受体蛋白,是参与上皮形态发生的Rho信号通路的一个新组分。18w突变体胚胎具有唾液腺内陷缺陷,类似于缺乏Rho通路组分的胚胎,并且18W的普遍表达导致Rho信号上调。反式杂合遗传相互作用和双突变分析表明,18W影响Rho-GTP酶信号通路并非通过Fog和RhoGEF2,而是通过抑制Rho GTP酶激活蛋白(RhoGAPs)。我们表明RhoGAP5A和RhoGAP88C/无交叉脉-c(CV-C)是正常唾液腺形态发生所必需的,这表明它们是18W的潜在靶点。

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