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人类WD重复蛋白WAIT-1特异性地与β7整合素的胞质尾相互作用。

The human WD repeat protein WAIT-1 specifically interacts with the cytoplasmic tails of beta7-integrins.

作者信息

Rietzler M, Bittner M, Kolanus W, Schuster A, Holzmann B

机构信息

Institute of Medical Microbiology, Immunology, and Hygiene, Technische Universität, Trogerstrasse 4a, D-81675 München, Germany.

出版信息

J Biol Chem. 1998 Oct 16;273(42):27459-66. doi: 10.1074/jbc.273.42.27459.

DOI:10.1074/jbc.273.42.27459
PMID:9765275
Abstract

Integrins of the beta7 subfamily, alpha4 beta7 and alphaE beta7, contribute to lymphocyte homing and to the development of protective or autoreactive immune responses at mucosal sites. The beta subunits of integrins are considered important for regulation of stimulated cell adhesion and adhesion-dependent signal transduction. Using a yeast interaction trap screen, a human WD repeat protein, termed WAIT-1, was isolated that interacts with the integrin beta7 cytoplasmic tail and is homologous to mouse EED and Drosophila ESC proteins. WAIT-1 also binds to the cytoplasmic domains of alpha4 and alphaE but not to those of integrin beta1, beta2, and alphaL subunits. Association of WAIT-1 and beta7-integrin was confirmed by coprecipitation from transiently transfected 293 cells. The binding site for WAIT-1 was mapped to a short membrane-proximal region of the beta7 cytoplasmic tail with Tyr-735 being of critical importance. Northern blot analysis revealed multiple WAIT-1-related transcripts with differential expression in circulating leukocytes, tissue-resident cells of diverse origin, and lymphoid malignancies. These results suggest that WAIT-1, together with the recently identified RACK1, may define a novel subfamily of WD repeat proteins that interact with distinct subsets of integrin cytoplasmic tails and may act as specific regulators of integrin function.

摘要

β7亚家族的整合素α4β7和αEβ7有助于淋巴细胞归巢以及在黏膜部位保护性或自身反应性免疫应答的发展。整合素的β亚基被认为对刺激细胞黏附及黏附依赖性信号转导的调节很重要。通过酵母相互作用陷阱筛选,分离出一种名为WAIT-1的人类WD重复蛋白,它与整合素β7的胞质尾相互作用,并且与小鼠EED和果蝇ESC蛋白同源。WAIT-1也与α4和αE的胞质结构域结合,但不与整合素β1、β2和αL亚基的胞质结构域结合。通过从瞬时转染的293细胞中共沉淀证实了WAIT-1与β7整合素的关联。WAIT-1的结合位点被定位到β7胞质尾的一个短的膜近端区域,其中酪氨酸735至关重要。Northern印迹分析揭示了多个WAIT-1相关转录本,它们在循环白细胞、不同来源的组织驻留细胞和淋巴样恶性肿瘤中差异表达。这些结果表明,WAIT-1与最近鉴定的RACK1一起,可能定义了一个WD重复蛋白的新亚家族,该亚家族与整合素胞质尾的不同亚群相互作用,并可能作为整合素功能的特异性调节剂。

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