[1] Castora FJ.Mitochondrial function and abnormalities implicated in ;the pathogenesis of ASD[J]. Progress in Neuro-Psychopharmaco-logy & Biological Psychiatry, 2018, 92:83-108. [2] Craven L, Alston CL, et al.Recent advances in mitochondrial dise-ase[J]. Annu Rev Genom Hum G, 2017, 18:257-275. [3] Devenish RJ, Prescott M, Roucou X, et al.Insights into ATP synthase assembly and function through the molecular genetic manipulation of subunits of the yeast mitochondrial enzyme complex[J]. Biochim Biophys Acta, 2000, 1458(2-3):428-442. [4] Malina C, Larsson C, Nielsen J.Yeast mitochondria:An overview of mitochondrial biology and the potential of mitochondrial systems biology[J]. FEMS Yeast Research, 2018, 18(5):1-17. [5] Herrnstadt C, Howell N.An evolutionary perspective on pathogenic mtdna mutations:Haplogroup associations of clinical disorders[J]. Mitochondrion, 2004, 4(5-6):791-798. [6] Baker BM, Haynes CM.Mitochondrial protein quality control during biogenesis and aging[J]. Trends Biochem Sci, 2011, 36(5):254-261. [7] Lasserre JP, Dautant A, Aiyar RS, et al.Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies[J]. Dis Model Mech, 2015, 8(6):509-526. [8] Alston CL, Rocha MC, Lax NZ, et al.The genetics and pathology of mitochondrial disease[J]. J Pathol, 2017, 241(2):236-250. [9] Van Der Bliek AM, Sedensky MM, Morgan PG. Cell biology of the mitochondrion[J]. Genetics, 2017, 207(3):843-871. [10] Soubannier V, Rusconi F, Vaillier J, et al.The second stalk of the yeast atp synthase complex:Identification of subunits showing cross-links with known positions of subunit 4(subunit b)[J]. Biochemistry, 1999, 38(45):15017-15024. [11] Mayr JA, Haack TB, Freisinger P, et al.Spectrum of combined respiratory chain defects[J]. Journal of Inherited Metabolic Disease, 2015, 38(4):629-640. [12] Davies KM, Anselmi C, et al.Structure of the yeast f1fo-atp synthase ;dimer and its role in shaping the mitochondrial cristae[J]. Proc Natl Acad Sci USA, 2012, 109(34):13602-13607. [13] Vo TD, Palsson BO.Building the power house:Recent advances in mitochondrial studies through proteomics and systems biology[J]. Am J Physiol-Cell Ph, 2007, 292(1):C164-C177. [14] Higuti T, Tsurumi C, Osaka F, et al.Molecular cloning of cDNA for the import precursor of human subunit b of H+ synthase in mitochondria[J]. Biochemical and Biophysical Research Communications, 1991, 178(3):1014-1020. [15] Foury F, Roganti T, Lecrenier N, et al.The complete sequence of the mitochondrial genome of saccharomyces cerevisiae[J]. FEBS Letters, 1998, 440(3):325-331. [16] Andersson SG, Zomorodipour A, Andersson JO, et al.The genome sequence of rickettsia prowazekii and the origin of mitochondria[J]. Nature, 1998, 396(6707):133-140. [17] Kwon YY, Choi KM, Cho C, et al.Mitochondrial efficiency-dependent viability of saccharomyces cerevisiae mutants carrying individual electron transport chain component deletions[J]. Molecules and Cells, 2015, 38(12):1054-1063. [18] Welch AK, Bostwick CJ, Cain BD.Manipulations in the peripheral stalk of the saccharomyces cerevisiae f1f0-atp synthase[J]. The Journal of Biological Chemistry, 2011, 286(12):10155-10162. [19] Weimann T, et al.The intermembrane space loop of subunit b(4)is a major determinant of the stability of yeast oligomeric atp synthases[J]. Biochem, 2008, 47(11):3556-3563. [20] Soubannier V, Vaillier J, Paumard P, et al.In the absence of the first membrane-spanning segment of subunit 4(b), the yeast atp synthase is functional but does not dimerize or oligomerize[J]. Journal of Biological Chemistry, 2002, 277(12):10739-10745. [21] Velours J, Arselin G, et al.The yeast atp synthase subunit 4:Structure and function[J]. Biochimie, 1989, 71(8):903-915. |