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盘基网柄菌多细胞形态发生需要一种具有类绒毛蛋白头部结构域的独特踝蛋白同源物。

A unique talin homologue with a villin headpiece-like domain is required for multicellular morphogenesis in Dictyostelium.

作者信息

Tsujioka M, Machesky L M, Cole S L, Yahata K, Inouye K

机构信息

Department of Botany, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.

出版信息

Curr Biol. 1999 Apr 8;9(7):389-92. doi: 10.1016/s0960-9822(99)80169-9.

Abstract

Molecules involved in the interaction between the extracellular matrix, cell membrane and cytoskeleton are of central importance in morphogenesis. Talin is a large cytoskeletal protein with a modular structure consisting of an amino-terminal membrane-interacting domain, with sequence similarities to members of the band 4.1 family, and a carboxy-terminal region containing F-actin-binding and vinculin-binding domains [1] [2]. It also interacts with the cytoplasmic tail of beta integrins which, on the external face of the membrane, bind to extracellular matrix proteins [3]. The possible roles of talin in multicellular morphogenesis in development remain largely unexplored. In Dictyostelium, a eukaryotic microorganism capable of multicellular morphogenesis, a talin homologue (TALA) has previously been identified and shown to play an important role in cell-to-substrate adhesion and maintenance of normal elastic properties of the cell [4] [5] [6]. Here, we describe a second talin homologue (TALB) that is required for multicellular morphogenesis in the development of Dictyostelium. Unlike any other talin characterised to date, it contains an additional carboxy-terminal domain homologous to the villin headpiece.

摘要

参与细胞外基质、细胞膜和细胞骨架之间相互作用的分子在形态发生过程中至关重要。踝蛋白是一种大型细胞骨架蛋白,具有模块化结构,由一个氨基末端膜相互作用结构域(其序列与4.1带家族成员相似)和一个羧基末端区域组成,该区域包含F-肌动蛋白结合域和纽蛋白结合域[1][2]。它还与β整合素的细胞质尾部相互作用,而β整合素在膜的外表面与细胞外基质蛋白结合[3]。踝蛋白在发育过程中的多细胞形态发生中的可能作用在很大程度上仍未被探索。在盘基网柄菌(一种能够进行多细胞形态发生的真核微生物)中,先前已鉴定出一种踝蛋白同源物(TALA),并表明其在细胞与底物的黏附以及细胞正常弹性特性的维持中起重要作用[4][5][6]。在此,我们描述了盘基网柄菌发育过程中多细胞形态发生所需的第二种踝蛋白同源物(TALB)。与迄今为止所表征的任何其他踝蛋白不同,它含有一个与绒毛蛋白头部结构域同源的额外羧基末端结构域。

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