Reid T, Furuyashiki T, Ishizaki T, Watanabe G, Watanabe N, Fujisawa K, Morii N, Madaule P, Narumiya S
Department of Pharmacology, Kyoto University Faculty of Medicine, Yoshida, Sakyo-ku, Kyoto 606, Japan.
J Biol Chem. 1996 Jun 7;271(23):13556-60. doi: 10.1074/jbc.271.23.13556.
Using a mouse embryo cDNA library, we conducted a two-hybrid screening to identify new partners for the small GTPase Rho. One clone obtained by this procedure contained a novel cDNA of 291 base pairs and interacted strongly with RhoA and RhoC, weakly with RhoB, and not at all with Rac1 and Cdc42Hs. Full-length cDNAs were then isolated from a mouse brain library. While multiple splicing variants were common, we identified three cDNAs with an identical open reading frame encoding a 61-kDa protein that we named rhotekin (from the Japanese "teki," meaning target). The N-terminal part of rhotekin, encoded by the initial cDNA and produced in bacteria as a glutathione S-transferase fusion protein, exhibited in vitro binding to 35S-labeled guanosine 5'-3-O-(thio)triphosphate-bound Rho, but not to Rac1 or Cdc42Hs in ligand overlay assays. In addition, this peptide inhibited both endogenous and GTPase-activating protein-stimulated Rho GTPase activity. The amino acid sequence of this region shares approximately 30% identity with the Rho-binding domains of rhophilin and a serine/threonine kinase, PKN, two other Rho target proteins that we recently identified (Watanabe, G., Saito, Y., Madaule, P., Ishizaki, T., Fujisawa, K., Morii, N., Mukai, H., Ono, Y., Kakizuka, A., and Narumiya, S. (1996) Science 271, 645-648). Thus, not only is rhotekin a novel partner for Rho, but it also belongs to a wide family of proteins that bear a consensus Rho-binding sequence at the N terminus. To our knowledge, this is the first conserved sequence for Rho effectors, and we have termed this region Rho effector motif class 1.
利用小鼠胚胎cDNA文库,我们进行了双杂交筛选以鉴定小GTP酶Rho的新结合蛋白。通过该方法获得的一个克隆包含一个291个碱基对的新cDNA,它与RhoA和RhoC强烈相互作用,与RhoB弱相互作用,与Rac1和Cdc42Hs完全不相互作用。然后从鼠脑文库中分离出全长cDNA。虽然多个剪接变体很常见,但我们鉴定出三个具有相同开放阅读框的cDNA,它们编码一个61 kDa的蛋白,我们将其命名为rhotekin(来自日语“teki”,意为靶标)。rhotekin的N端部分由最初的cDNA编码,并作为谷胱甘肽S-转移酶融合蛋白在细菌中产生,在配体覆盖分析中显示其在体外与35S标记的鸟苷5'-3-O-(硫代)三磷酸结合的Rho结合,但不与Rac1或Cdc42Hs结合。此外,该肽抑制内源性和GTP酶激活蛋白刺激的Rho GTP酶活性。该区域的氨基酸序列与rhotekin和丝氨酸/苏氨酸激酶PKN的Rho结合结构域具有约30%的同一性,PKN是我们最近鉴定的另外两个Rho靶蛋白(Watanabe, G., Saito, Y., Madaule, P., Ishizaki, T., Fujisawa, K., Morii, N., Mukai, H., Ono, Y., Kakizuka, A., and Narumiya, S. (1996) Science 271, 645 - 648)。因此,rhotekin不仅是Rho的一个新结合蛋白,而且它还属于一个在N端带有共有Rho结合序列的广泛蛋白家族。据我们所知,这是Rho效应蛋白的第一个保守序列,我们将该区域称为Rho效应基序1类。