Klanner C, Prokisch H, Langer T
Institut für Physiologische Chemie, Universität München, 81377 München, Germany.
Mol Biol Cell. 2001 Sep;12(9):2858-69. doi: 10.1091/mbc.12.9.2858.
Eukaryotic AAA proteases form a conserved family of membrane-embedded ATP-dependent proteases but have been analyzed functionally only in the yeast Saccharomyces cerevisiae. Here, we have identified two novel members of this protein family in the filamentous fungus Neurospora crassa, which were termed MAP-1 and IAP-1. Both proteins are localized to the inner membrane of mitochondria. They are part of two similar-sized high molecular mass complexes, but expose their catalytic sites to opposite membrane surfaces, namely, the intermembrane and the matrix space. Disruption of iap-1 by repeat-induced point mutation caused a slow growth phenotype at high temperature and stabilization of a misfolded inner membrane protein against degradation. IAP-1 could partially substitute for functions of its yeast homolog Yme1, demonstrating functional conservation. However, respiratory growth at 37 degrees C was not restored. Our results identify two components of the quality control system of the mitochondrial inner membrane in N. crassa and suggest that AAA proteases with catalytic sites exposed to opposite membrane surfaces are present in mitochondria of all eukaryotic cells.
真核生物的AAA蛋白酶构成了一个保守的膜嵌入型ATP依赖蛋白酶家族,但目前仅在酿酒酵母中对其进行了功能分析。在此,我们在丝状真菌粗糙脉孢菌中鉴定出了该蛋白家族的两个新成员,分别命名为MAP-1和IAP-1。这两种蛋白均定位于线粒体内膜。它们是两个大小相似的高分子量复合物的组成部分,但它们的催化位点朝向相反的膜表面,即膜间隙和线粒体基质空间。通过重复诱导点突变破坏iap-1会导致高温下生长缓慢的表型,并使错误折叠的内膜蛋白稳定而不被降解。IAP-1可以部分替代其酵母同源物Yme1的功能,证明了功能保守性。然而,在37℃下的呼吸生长并未恢复。我们的结果鉴定出了粗糙脉孢菌线粒体内膜质量控制系统的两个组成部分,并表明催化位点朝向相反膜表面的AAA蛋白酶存在于所有真核细胞的线粒体中。