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［1］Martin M, Cho J, Cesare AJ, et al. Termination factor-mediated DNA loop between termination and initiation sites drives mitochondrial rRNA synthesis［J］.Cell,2005, 123 (7):1227-1240.
［2］Hyvarinen AK, Kumanto MK, Marjavaara SK, et al. Effects on mitochondrial transcription of manipulating mTERF protein levels in cultured human HEK293 cells［J］. BMC Mol Biol, 2010,11:72.
［3］Huang W, Yu M, Jiao Y, et al. Mitochondrial transcription termination factor 2 binds to entire mitochondrial DNA and negatively regulates mitochondrial gene expression［J］.Acta Biochim Biophys Sin (Shanghai), 2011,43(6):472-479.
［4］Wredenberg A, Lagouge M, Bratic A, et al. MTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals［J］. PLoS Genet, 2013,9(1):e1003178.
［5］Metodiev MD, Spahr H, Loguercio Polosa P, et al. NSUN4 is a dual function mitochondrial protein required for both methylation of 12S rRNA and coordination of mitoribosomal assembly［J］. PLoS Genet, 2014,10(2):e1004110.
［6］Ye X, Han Y, Zhang L,et al. MTERF4 regulates the mitochondrial dysfunction induced by MPP(+) in SH-SY5Y cells［J］. Biochem Biophys Res Commun, 2015,464(1):214-220.
［7］Han Y, Gao P, Qiu S, et al. MTERF2 contributes to MPP+ -induced mitochondrial dysfunction and cell damage ［J］.Biochem Biophys Res Commun, 2016,471(1):177-183.
［8］Reinhardt P, Schmid B, Burbulla LF, et al.Genetic correction of a LRRK2 mutation in human iPSCs linksparkinsonian neurodegeneration to ERK-dependent changes in gene expression［J］.Cell Stem Cell,2013,12(3):354-367.
［9］Sohn EJ, Shin MJ, Kim DW, et al. Tat-fused recombinant human SAG prevents dopaminergic neurodegeneration in a MPTP-induced Parkinson’s disease model［J］.Mol Cells, 2014,37(3):226-233.
［10］Hwang DS, Kim HG, Jang JB, et al. Dangguijakyak-san protects against 1-methyl-4-phenyl-1,2,3,6,-tetrahydropyridine-induced neuronal damage via anti-inflammatory action［J］.Evid Based Complement Alternat Med, 2013,2013:976270.
［11］Roberti M, Polosa PL, Bruni F, et al. The MTERF family proteins: mitochondrial transcription regulators and beyond［J］. Biochim Biophys Acta, 2009,1787(5):303-311.
［12］Guja KE, Garcia-Diaz M. Hitting the brakes: termination of mitochondrial transcription［J］. Biochim Biophys Acta, 2012,1819(9-10):939-947.
［13］Fernandez-Silva P, Martinez-Azorin F, Micol V, et al. The human mitochondrial transcription termination factor (mTERF) is a multizipper protein but binds to DNA as a monomer, with evidence pointing to intramolecular leucine zipper interactions［J］. EMBO J, 1997,16 (5):1066-1079.
［14］Kruse B, Narasimhan N, Attardi G. Termination of transcription in human mitochondria: identifi-cation and purification of a DNA binding protein factor that promotes termination ［J］. Cell, 1989, 58(2) : 391-397.
［15］Park CB, Asin-Cayuela J, Camara Y, et al. MTERF3 is a negative regulator of mammalian mtDNA transcription［J］. Cell, 2007, 130(2):273-285.
［16］Spahr H, Samuelsson T, Hallberg BM, et al. Structure of mitochondrial transcriptiontermination factor 3 reveals a novel nucleic acid-binding domain［J］. Biochem Biophys Res Commun,2010,397(3):386-390.
［17］Camara Y, Asin-Cayuela J, Park CB, et al. MTERF4 regulates translation by targeting the methyltransferase NSUN4 to the mammalian mitochondrialribosome［J］. Cell Metab, 2011,13(5):527-539.
［18］Yakubovskaya E, Guja KE, Mejia E, et al. Structure of the essential MTERF4 : NSUN4 protein complex reveals how an MTERF protein collaborates to facilitate rRNA modification［J］. Structure,2012,20(11):1940-1947.
［19］Terzioglu M, Ruzzenente B, Harmel J, et al. MTERF1 binds mtDNA to prevent transcriptional interference at the light-strand promoter but is dispensable for rRNA gene transcription regulation［J］. Cell Metab, 2013, 17(4):618-626.
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