Witke W, Hofmann A, Köppel B, Schleicher M, Noegel A A
Max-Planck-Institute for Biochemistry, Martinsried, Germany.
J Cell Biol. 1993 May;121(3):599-606. doi: 10.1083/jcb.121.3.599.
Dictyostelium alpha-actinin is a Ca(2+)-regulated F-actin cross-linking protein. To test the inhibitory function of the two EF hands, point mutations were introduced into either one or both Ca(2+)-binding sites. After mutations, the two EF hands were distinguishable with respect to their regulatory activities. Inactivation of EF hand I abolished completely the F-actin cross-linking activity of Dictyostelium discoideum alpha-actinin but Ca2+ binding by EF hand II was still observed in a 45Ca2+ overlay assay. In contrast, after mutation of EF hand II the molecule was still active and inhibited by Ca2+; however, approximately 500-fold more Ca2+ was necessary for inhibition and 45Ca2+ binding could not be detected in the overlay assay. These data indicate that EF hand I has a low affinity for Ca2+ and EF hand II a high affinity, implying a regulatory function of EF hand I in the inhibition of F-actin cross-linking activity. Biochemical data is presented which allows us to distinguish two functions of the EF hand domains in D. discoideum alpha-actinin: (a) at the level of the EF-hands, the Ca(2+)-binding affinity of EF hand I was increased by EF hand II in a cooperative manner, and (b) at the level of the two subunits, the EF hands acted as an on/off switch for actin-binding in the neighboring subunit. To corroborate in vitro observations in an in vivo system we tried to rescue the abnormal phenotype of a mutant (Witke, W., M. Schleicher, A. A. Noegel. 1992. Cell. 68:53-62) by introducing the mutated alpha-actinin cDNAs. In agreement with the biochemical data, only the molecule modified in EF hand II could rescue the abnormal phenotype. Considering the fact that the active construct is "always on" because it requires nonphysiological, high Ca2+ concentrations for inactivation, it is interesting to note that an unregulated alpha-actinin was able to rescue the mutant phenotype.
盘基网柄菌α-辅肌动蛋白是一种受Ca(2+)调节的F-肌动蛋白交联蛋白。为了测试两个EF手型结构域的抑制功能,在一个或两个Ca(2+)结合位点引入了点突变。突变后,两个EF手型结构域在调节活性方面有所不同。EF手型结构域I失活完全消除了盘基网柄菌α-辅肌动蛋白的F-肌动蛋白交联活性,但在45Ca2+覆盖分析中仍观察到EF手型结构域II与Ca2+结合。相反,EF手型结构域II突变后,该分子仍有活性且受Ca2+抑制;然而,抑制所需的Ca2+浓度大约高500倍,且在覆盖分析中检测不到45Ca2+结合。这些数据表明,EF手型结构域I对Ca2+的亲和力低,而EF手型结构域II对Ca2+的亲和力高,这意味着EF手型结构域I在抑制F-肌动蛋白交联活性方面具有调节功能。本文给出的生化数据使我们能够区分盘基网柄菌α-辅肌动蛋白中EF手型结构域的两种功能:(a) 在EF手型结构域水平,EF手型结构域II以协同方式提高了EF手型结构域I的Ca(2+)结合亲和力,(b) 在两个亚基水平,EF手型结构域作为相邻亚基中肌动蛋白结合的开/关开关。为了在体内系统中证实体外观察结果,我们试图通过引入突变的α-辅肌动蛋白cDNA来挽救一个突变体(Witke, W., M. Schleicher, A. A. Noegel. 1992. Cell. 68:53 - 62)的异常表型。与生化数据一致,只有在EF手型结构域II中修饰的分子能够挽救异常表型。考虑到活性构建体“一直处于开启状态”,因为它需要非生理的高Ca2+浓度才能失活,值得注意的是,一种不受调节的α-辅肌动蛋白能够挽救突变体表型。