Nagata Koh-Ichi, Ito Hidenori, Iwamoto Ikuko, Morishita Rika, Asano Tomiko
Department of Molecular Neurobiology, Institute for Developmental Research, Aichi Human Service Center, 713-8 Kamiya, Kasugai, Aichi, 480-0392, Japan.
Med Mol Morphol. 2009 Mar;42(1):9-15. doi: 10.1007/s00795-008-0433-8. Epub 2009 Mar 18.
Among various effector proteins for the Rho small GTPase, the function(s) of Rhotekin is almost unknown. We have identified a multi-domain adaptor protein, vinexin, as a binding partner for Rhotekin, using yeast two-hybrid screening of a human heart library. Rhotekin was found to associate with vinexin in vitro, in COS7 cells, and in brain tissues. The C-terminal Pro-rich motif of Rhotekin exhibited binding to the third SH3 domain of vinexin. The binding was little affected by Rho but was inhibited by activated Cdc42 in COS7 cells. Immunofluorescence analyses revealed partial colocalization of vinexin-alpha with Rhotekin at focal adhesions in REF52 fibroblast cells. These results suggest that Rhotekin forms a complex with vinexin and may play a role at focal adhesions.
在Rho小GTP酶的各种效应蛋白中,Rhotekin的功能几乎未知。我们通过对人心脏文库进行酵母双杂交筛选,鉴定出一种多结构域衔接蛋白——纽蛋白(vinexin)作为Rhotekin的结合伴侣。在体外、COS7细胞和脑组织中均发现Rhotekin与纽蛋白相关联。Rhotekin的C末端富含脯氨酸基序与纽蛋白的第三个SH3结构域表现出结合。在COS7细胞中,这种结合几乎不受Rho的影响,但被激活的Cdc42抑制。免疫荧光分析显示,在REF52成纤维细胞的粘着斑处,纽蛋白α与Rhotekin部分共定位。这些结果表明,Rhotekin与纽蛋白形成复合物,并可能在粘着斑处发挥作用。