Zeng Xiaomei, Hourset Audrey, Tzagoloff Alexander
Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
Genetics. 2007 Jan;175(1):55-63. doi: 10.1534/genetics.106.065821. Epub 2006 Nov 16.
Mutations in the Saccharomyces cerevisiae ATP22 gene were previously shown to block assembly of the F0 component of the mitochondrial proton-translocating ATPase. Further inquiries into the function of Atp22p have revealed that it is essential for translation of subunit 6 of the mitochondrial ATPase. The mutant phenotype can be partially rescued by the presence in the same cell of wild-type mitochondrial DNA and a rho- deletion genome in which the 5'-UTR, first exon, and first intron of COX1 are fused to the fourth codon of ATP6. The COX1/ATP6 gene is transcribed and processed to the mature mRNA by splicing of the COX1 intron from the precursor. The hybrid protein translated from the novel mRNA is proteolytically cleaved at the normal site between residues 10 and 11 of the subunit 6 precursor, causing the release of the polypeptide encoded by the COX1 exon. The ability of the rho- suppressor genome to express subunit 6 in an atp22 null mutant constitutes strong evidence that translation of subunit 6 depends on the interaction of Atp22p with the 5'-UTR of the ATP6 mRNA.
先前的研究表明,酿酒酵母ATP22基因的突变会阻止线粒体质子转运ATP酶F0组分的组装。对Atp22p功能的进一步研究发现,它对于线粒体ATP酶亚基6的翻译至关重要。在同一细胞中存在野生型线粒体DNA和rho-缺失基因组(其中COX1的5'-UTR、第一个外显子和第一个内含子与ATP6的第四个密码子融合)时,突变表型可以得到部分挽救。COX1/ATP6基因转录后,通过从前体中剪接COX1内含子加工成成熟mRNA。从新mRNA翻译出的杂合蛋白在亚基6前体第10和11位残基之间的正常位点被蛋白水解切割,导致COX1外显子编码的多肽释放。rho-抑制基因组在atp22缺失突变体中表达亚基6的能力构成了强有力的证据,表明亚基6的翻译依赖于Atp22p与ATP6 mRNA的5'-UTR之间的相互作用。