Talin is essential for integrin function in Drosophila

被引:216
作者
Brown, NH [1 ]
Gregory, SL
Rickoll, WL
Fessler, LI
Prout, M
White, RAH
Fristrom, JW
机构
[1] Univ Cambridge, Wellcome Trust Canc Res UK Inst, Cambridge CB2 1QR, England
[2] Univ Cambridge, Dept Anat, Cambridge CB2 3DY, England
[3] Univ Puget Sound, Dept Biol, Tacoma, WA 98416 USA
[4] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
[6] Univ Calif Berkeley, Div Genet & Dev, Berkeley, CA 94750 USA
[7] Univ Calif Berkeley, Dept Mol & Cellular Biol, Berkeley, CA 94750 USA
关键词
D O I
10.1016/S1534-5807(02)00290-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We show that the Drosophila gene rhea, isolated because its wing blister phenotype is typical of mutants affecting integrin function, encodes talin. Embryos deficient in talin have very similar phenotypes to integrin (betaPS) null embryos, including failure in germ band retraction and muscle detachment. We demonstrate that talin is not required for the presence of integrins on the cell surface or their localization at muscle termini. However, talin is required for formation of focal adhesion-like clusters of integrins on the basal surface of imaginal disc epithelia and junctional plaques between muscle and tendon cells. These results indicate that talin is essential for integrin function and acts by stably linking clusters of ECM-linked integrins to the cytoskeleton.
引用
收藏
页码:569 / 579
页数:11
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