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2
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本文引用的文献

1
The 70 kDa S6 kinase complexes with and is activated by the Rho family G proteins Cdc42 and Rac1.70千道尔顿的S6激酶与Rho家族G蛋白Cdc42和Rac1结合并被其激活。
Cell. 1996 May 17;85(4):573-83. doi: 10.1016/s0092-8674(00)81257-x.
2
The Ras-related GTPase Rac1 binds tubulin.与Ras相关的GTP酶Rac1与微管蛋白结合。
J Biol Chem. 1996 Feb 16;271(7):3756-62. doi: 10.1074/jbc.271.7.3756.
3
LET-23 receptor localization by the cell junction protein LIN-7 during C. elegans vulval induction.秀丽隐杆线虫外阴诱导过程中,细胞连接蛋白LIN-7对LET-23受体的定位作用。
Cell. 1996 Apr 19;85(2):195-204. doi: 10.1016/s0092-8674(00)81096-x.
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Actin-based cell motility and cell locomotion.基于肌动蛋白的细胞运动和细胞迁移。
Cell. 1996 Feb 9;84(3):371-9. doi: 10.1016/s0092-8674(00)81281-7.
5
Tissue polarity genes of Drosophila regulate the subcellular location for prehair initiation in pupal wing cells.果蝇的组织极性基因调控着蛹期翅细胞中前毛起始的亚细胞定位。
J Cell Biol. 1993 Oct;123(1):209-21. doi: 10.1083/jcb.123.1.209.
6
The distribution of PS integrins, laminin A and F-actin during key stages in Drosophila wing development.果蝇翅膀发育关键阶段中PS整合素、层粘连蛋白A和F-肌动蛋白的分布。
Development. 1993 Feb;117(2):509-23. doi: 10.1242/dev.117.2.509.
7
The Drosophila segment polarity gene dishevelled encodes a novel protein required for response to the wingless signal.果蝇体节极性基因“凌乱”编码一种对无翅信号作出反应所需的新型蛋白质。
Genes Dev. 1994 Jan;8(1):118-30. doi: 10.1101/gad.8.1.118.
8
Planar polarity in the ciliated epidermis of Xenopus embryos.非洲爪蟾胚胎纤毛表皮中的平面极性
Dev Biol. 1993 Dec;160(2):355-68. doi: 10.1006/dbio.1993.1312.
9
The frizzled gene of Drosophila encodes a membrane protein with an odd number of transmembrane domains.
Mech Dev. 1994 Feb;45(2):127-37. doi: 10.1016/0925-4773(94)90026-4.
10
Drosophila singed, a fascin homolog, is required for actin bundle formation during oogenesis and bristle extension.果蝇的“signed”基因是一种成束蛋白同源物,在卵子发生和刚毛延伸过程中,肌动蛋白束的形成需要该基因。
J Cell Biol. 1994 Apr;125(2):369-80. doi: 10.1083/jcb.125.2.369.

Rac1和Cdc42在果蝇翅膀平面极化和刚毛生长中的作用。

Roles for Rac1 and Cdc42 in planar polarization and hair outgrowth in the wing of Drosophila.

作者信息

Eaton S, Wepf R, Simons K

机构信息

Programme in Cell Biology, European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

J Cell Biol. 1996 Dec;135(5):1277-89. doi: 10.1083/jcb.135.5.1277.

DOI:10.1083/jcb.135.5.1277
PMID:8947551
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2121092/
Abstract

The wing of Drosophila melanogaster is covered by an array of distally pointing hairs. A hair begins as a single membrane outgrowth from each wing epithelial cell, and its distal orientation is determined by the restriction of outgrowth to a single distal site on the cell circumference (Wong, L., and P. Adler. 1993. J. Cell Biol. 123:209-211.). We have examined the roles of Cdc42 and Rac1 in the formation of wing hairs. We find that Cdc42 is required for localized actin polymerization in the extending hair. Interfering with Cdc42 activity by expression of a dominant negative protein abolishes both localized actin polymerization and hair outgrowth. In contrast, Rac1 is important for restricting the site at which hairs grow out. Cells expressing the dominant negative Rac1N17 fail to restrict outgrowth to a single site and give rise to multiple wing hairs. This polarity defect is associated with disturbances in the organization of junctional actin and also with disruption of an intricate microtubule network that is intimately associated with the junctional region. We also find that apical junctions and microtubules are involved in structural aspects of hair outgrowth. During hair formation, the apical microtubules that point distally elongate and fill the emerging wing hair. As the hair elongates, junctional proteins are reorganized on the proximal and distal edges of each cell.

摘要

黑腹果蝇的翅膀覆盖着一系列向远端伸出的刚毛。每根刚毛最初是从每个翅膀上皮细胞伸出的单个膜状突起,其远端方向是由突起限制在细胞圆周上的单个远端位点所决定的(Wong, L., and P. Adler. 1993. J. Cell Biol. 123:209 - 211.)。我们研究了Cdc42和Rac1在翅膀刚毛形成中的作用。我们发现Cdc42是延伸中的刚毛中局部肌动蛋白聚合所必需的。通过表达显性负性蛋白干扰Cdc42活性会消除局部肌动蛋白聚合和刚毛生长。相反,Rac1对于限制刚毛长出的位点很重要。表达显性负性Rac1N17的细胞不能将生长限制在单个位点,而是长出多根翅膀刚毛。这种极性缺陷与连接肌动蛋白组织的紊乱以及与连接区域密切相关的复杂微管网络的破坏有关。我们还发现顶端连接和微管参与了刚毛生长的结构方面。在刚毛形成过程中,向远端延伸的顶端微管伸长并填充新生的翅膀刚毛。随着刚毛伸长,连接蛋白在每个细胞的近端和远端边缘重新组织。