Chen X J, Clark-Walker G D
Molecular and Population Genetics Group, Research School of Biological Sciences, Australian National University, Canberra, Australia.
Genetics. 1996 Dec;144(4):1445-54. doi: 10.1093/genetics/144.4.1445.
In a previous report, we found that mutations at the mitochondrial genome integrity locus, MGI1, can convert Kluyveromyces lactis into a petite-positive yeast. In this report, we describe the isolation of the MGI1 gene and show that it encodes the beta-subunit of the mitochondrial F1-ATPase. The site of mutation in four independently isolated mgi1 alleles is at Arg435, which has changed to Gly in three cases and Ile in the fourth isolate. Disruption of MGI1 does not lead to the production of mitochondrial genome deletion mutants, indicating that an assembled F1 complex is needed for the "gain-of-function" phenotype found in mgi1 point mutants. The location of Arg435 in the beta-subunit, as deduced from the three-dimensional structure of the bovine F1-ATPase, together with mutational sites in the previously identified mgi2 and mgi5 alleles, suggests that interaction of the beta- and alpha- (MGI2) subunits with the gamma-subunit (MGI5) is likely to be affected by the mutations.
在之前的一份报告中,我们发现线粒体基因组完整性位点MGI1处的突变可将乳酸克鲁维酵母转化为小菌落阳性酵母。在本报告中,我们描述了MGI1基因的分离,并表明它编码线粒体F1 - ATP合酶的β亚基。四个独立分离的mgi1等位基因中的突变位点位于Arg435,在三个案例中该位点已变为甘氨酸,在第四个分离株中变为异亮氨酸。MGI1的破坏不会导致线粒体基因组缺失突变体的产生,这表明组装好的F1复合物是mgi1点突变体中发现的“功能获得”表型所必需的。根据牛F1 - ATP合酶的三维结构推断,Arg435在β亚基中的位置,以及先前鉴定的mgi2和mgi5等位基因中的突变位点,表明β亚基和α亚基(MGI2)与γ亚基(MGI5)的相互作用可能会受到这些突变的影响。