[1] VO T D,PALSSON B O. Building the power house:recent advances in mitochondrial studies through proteomics and systems biology[J]. American journal of physiology-cell physiology,2007,292(1):164-177.
[2]LURIN C1,ANDRéS C,AUBOURG S,et al. Genome-wide analysis of Arabidopsis pentatricopeptide repeat proteins reveals their essential role in organelle biogenesis[J]. Plant cell,2004,16(8):2089-2103.
[3]PAPA S,SCACCO S,SCHLIEBS M,et al. Mitochondrial diseases and aging[J]. Molecular aspects of medicine,1996,17(6):513-563.
[4]RAULE N,SEVINI F,SANTORO A,et al. Association studies on human mitochondrial DNA:methodological aspects and results in the most common age-related diseases[J]. Mitochondrion,2007,7(1/2):29-38.
[5]DOWLING D K. Evolutionary perspectives on the links between mitochondrial genotype and disease phenotype.[J]. Biochimica Et Biophysica Acta,2014,1840(4):1393-1403.
[6]SCHON E A,DIMAURO S,HIRANO M. Human mitochondrial DNA:roles of inherited andsomatic mutations[J]. Nature reviews genetics,2012,13(12):878-890.
[7]NEWSHOLME P,GAUDEL C,KRAUSE M. Mitochondria and diabetes:an intriguing pathogenetic role[J]. Advances in experimental medicine and biology,2012(942):235-247.
[8]JAMES A M,COLLINS Y,LOGAN A,et al. Mitochondrial oxidative stress and the metabolic syndrome[J]. Trends in endocrinology and metabolism,2012,23(9):429-434.
[9]HATAKEYAMA H,GOTO Y I. Respiratory chain complex disorganization impairs mitochondrial and cellular integrity:phenotypic variation in cytochrome c oxidase deficiency[J]. American journal of pathology,2017,187(1):110-121.
[10]MAYR J A,HAACK T B,FREISINGER P,et al. Spectrum of combined respiratory chain de fects[J]. Journal of inherited metabolic disease,2015,38(4):629-640.
[11]ROLOFF G A,HENRY M F. Mam33 promotes cytochrome c oxidase subunit I translation in Saccharomyces cerevisiae mitochondria[J]. Molecular biology of the cell,2015,26(16):2885-2894.
[12]CROSS R L. The mechanism and regulation of ATP synthesis by F1-ATPases[J]. Annu Rev Biochem,1981,50:681-714.
[13]WALKER J E,FEARNLEY I M,GAY N J,et al. Primary structure and subunit stoichiometry of F1-ATPase from bovine mitochondria[J]. Journal of molecular biology,1985,184(4):677-701.
[14]FUTAI M,KANAZAWA H. Structure and function of proton-translocating adenosine triphosphatase(F0F1):biochemical and molecular biological approaches[J]. Microbiological reviews,1983,47(3):285-312.
[15]TZAGOLOFF A,MEAGHER P. Assembly of the mitochondrial membrane system. V. properties of a dispersed preparation of the rutamycin-sensitive adenosine triphosphatase of yeast mitochondria[J]. The journal of biological chemistry,1971,246(23):7328-7336.
[16]ALEXANDER T,ANTONI B,WALTER N,et al. Atp10p assists assembly of Atp6p into the Fo unit of the yeast mitochondrial ATPase[J]. The journal of biological chemistry,2004,279(19):19775-19780.
[17]CLAROS M G,VINCENS P. Computational method to predict mitochondrially imported proteins and their targeting sequences[J]. European journal of biochemistry,1996,241(3):779-786.
[18]岳强,周惠. 粟酒裂殖酵母——一种良好的真核模式生物[J]. 韶关学院学报,2003,24(3):100-102.
[19]黄敏. 基因敲除技术及其应用[J]. 广东轻工职业技术学院学报,2009,8(4):12-14.
[20]PAUL M F,BARRIENTOS A,TZAGOLOFF A. A single amino acid change in subunit 6 of theyeast mitochondrial ATPase suppresses a nullmutation in ATP10[J]. The journal of biological chemistry,2000,275(38):29238-29243.
[21]DE J P,VAN DIJKEN J P,PRONK J T. Metabolic fluxes in chemostat cultures of Schizosaccharomyces pombe grown on mixtures of glucose and ethanol[J]. Microbiology,1996,142(6):1399-1407.