Clark-Walker G D, Francois F, Chen X J, Vieira Da Silva M R, Claisse M L
Molecular and Population Genetics Group, Research School of Biological Sciences, The Australian National University, GPO Box 475, Canberra City, ACT 2601, Australia.
Curr Genet. 1997 Jun;31(6):488-93. doi: 10.1007/s002940050234.
Specific mutations in nuclear MGI genes encoding the alpha, beta and gamma subunits of the mitochondrial inner membrane F1-ATPase complex allow mitochondrial DNA (mtDNA) to be lost from K. lactis. In the absence of a mutation in any of these three nuclear genes, loss of mtDNA is lethal. These results imply that mtDNA encodes a gene that is essential. Likely candidates for such an essential role are the ATP6, 8 and 9 genes coding for proteins of the ATP synthase-F0 component. The present study removes ATP9 from contention as a vital mitochondrial gene because in a respiratory deficient mutant, Gly- 3. 9, lacking a nuclear mgi mutation, we have found that a rearrangement in mtDNA has deleted 22 amino acids from the carboxy terminus of the 75 amino-acid subunit-9 protein. Rearrangement in mtDNA has occurred by recombination at a 23-bp repeated sequence in the introns of the ATP9 and large ribosomal RNA (LSU) subunit genes. These two introns, of 394 (ATP9) and 410 (LSU) nucleotides, both belong to group 1.
编码线粒体内膜F1 - ATP酶复合体α、β和γ亚基的核MGI基因中的特定突变,会导致乳酸克鲁维酵母的线粒体DNA(mtDNA)丢失。在这三个核基因中若没有任何一个发生突变,mtDNA的丢失是致死性的。这些结果表明mtDNA编码了一个必需基因。在ATP合酶F0组分的蛋白质编码基因ATP6、8和9中,可能存在这样一个发挥必需作用的基因。本研究排除了ATP9作为重要线粒体基因的可能性,因为在一个缺乏核mgi突变的呼吸缺陷型突变体Gly - 3.9中,我们发现mtDNA的重排从75个氨基酸的亚基9蛋白的羧基末端删除了22个氨基酸。mtDNA的重排是通过ATP9和大核糖体RNA(LSU)亚基基因内含子中一个23bp重复序列处的重组发生的。这两个内含子,分别为394个核苷酸(ATP9)和410个核苷酸(LSU),均属于第1类。