Suppr超能文献

Rho的不同区域决定了不同类别的Rho靶分子的Rho选择性结合。

Different regions of Rho determine Rho-selective binding of different classes of Rho target molecules.

作者信息

Fujisawa K, Madaule P, Ishizaki T, Watanabe G, Bito H, Saito Y, Hall A, Narumiya S

机构信息

Department of Pharmacology, Kyoto University Faculty of Medicine, Sakyo-ku, Kyoto 606, Japan.

出版信息

J Biol Chem. 1998 Jul 24;273(30):18943-9. doi: 10.1074/jbc.273.30.18943.

Abstract

Based on their Rho binding motifs several Rho target molecules can be classified into three groups; class I includes the protein kinase PKN, rhophilin, and rhotekin, class II includes the protein kinases, Rho-associated coiled-coil containing protein kinases, ROCK-I and ROCK-II, and class III includes citron. Taking advantage of the selectivity in recognition by these targets between Rho and Rac, we examined the regions in Rho required for selective binding of each class of Rho target molecules. Yeast two-hybrid assays were performed using Rho/Rac chimeras and either rhophilin, ROCK-I, or citron. This study showed the existence of at least two distinct regions in Rho (amino acids 23-40 and 75-92) that are critical for the selective binding of these targets. The former was required for binding to citron, whereas the latter was necessary for binding to rhophilin. On the other hand, either region showed affinity to ROCK-I. This was further confirmed by ligand overlay assay using both recombinant ROCK-I and ROCK-II proteins. Consistently, Rho/Rac chimeras containing either region can induce stress fibers in transfected HeLa cells, and this induction is suppressed by treatment with Y-27632, a specific inhibitor of ROCK kinases. These results suggest that the selective binding of different classes of Rho targets to Rho is determined by interaction between distinct Rho-binding motifs of the targets and different regions of Rho.

摘要

基于其Rho结合基序,几种Rho靶分子可分为三类;第一类包括蛋白激酶PKN、亲Rho蛋白和Rho结合蛋白,第二类包括蛋白激酶、含Rho相关卷曲螺旋的蛋白激酶ROCK-I和ROCK-II,第三类包括citron。利用这些靶分子对Rho和Rac识别的选择性,我们研究了每类Rho靶分子选择性结合所需的Rho区域。使用Rho/Rac嵌合体和亲Rho蛋白、ROCK-I或citron进行酵母双杂交实验。这项研究表明,Rho中至少存在两个不同区域(氨基酸23 - 40和75 - 92)对这些靶分子的选择性结合至关重要。前者是与citron结合所必需的,而后者是与亲Rho蛋白结合所必需的。另一方面,任一区域都显示出与ROCK-I有亲和力。使用重组ROCK-I和ROCK-II蛋白进行的配体覆盖分析进一步证实了这一点。一致地,含有任一区域的Rho/Rac嵌合体可在转染的HeLa细胞中诱导应力纤维,并且这种诱导可被ROCK激酶的特异性抑制剂Y-27632处理所抑制。这些结果表明,不同类别的Rho靶分子与Rho的选择性结合是由靶分子不同的Rho结合基序与Rho不同区域之间的相互作用决定的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验