The mitochondrial genome: structure, transcription, translation and replication.
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[1] S. Dimauro,et al. mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases. , 1991, American journal of human genetics.
[2] O. Gotoh,et al. Strictly maternal inheritance of rat mitochondrial DNA. , 1978, Biochemical and biophysical research communications.
[3] Cheng Yang,et al. Crystal structure of human mitochondrial single-stranded DNA binding protein at 2.4 Å resolution , 1997, Nature Structural Biology.
[4] H. Kasamatsu,et al. Replication of circular DNA in eukaryotic cells. , 1974, Annual review of biochemistry.
[5] G. Kawai,et al. A novel modified nucleoside found at the first position of the anticodon of methionine tRNA from bovine liver mitochondria. , 1994, Biochemistry.
[6] M. Holtrop,et al. Regulation of the expression of mitochondrial proteins: relationship between mtDNA copy number and cytochrome-c oxidase activity in human cells and tissues. , 1993, Biochimica et biophysica acta.
[7] Epler Jl,et al. N-formylmethionyl transfer ribonucleic acid in mitochondria from Neurospora. , 1970 .
[8] E. Schon,et al. Point mutations in the mitochondrial tRNA Lys gene: Implications for pathogenesis and mechanism , 1997 .
[9] V. Dubowitz,et al. Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion. , 1994, Human molecular genetics.
[10] Y. Kagawa,et al. Smaller isoform of human mitochondrial transcription factor 1: its wide distribution and production by alternative splicing. , 1993, Biochemical and biophysical research communications.
[11] D. Chang,et al. The gene for the RNA component of the mitochondrial RNA-processing endoribonuclease is located on human chromosome 9p and on mouse chromosome 4. , 1990, Genomics.
[12] B. Xu,et al. Assignment of a yeast protein necessary for mitochondrial transcription initiation. , 1992, Nucleic acids research.
[13] N. Martin,et al. Yeast mitochondrial RNase P. Sequence of the RPM2 gene and demonstration that its product is a protein subunit of the enzyme. , 1993, The Journal of biological chemistry.
[14] M. Saraste,et al. FEBS Lett , 2000 .
[15] N. Martin,et al. Dramatic size variation of yeast mitochondrial RNAs suggests that RNase P RNAs can be quite small. , 1991, The Journal of biological chemistry.
[16] G. Attardi,et al. Synthesis and turnover of mitochondrial ribonucleic acid in HeLa cells: the mature ribosomal and messenger ribonucleic acid species are metabolically unstable , 1981, Molecular and cellular biology.
[17] Y. Hirao,et al. Fate of sperm tail components after incorporation into the hamster egg. , 1988, Gamete research.
[18] D. Nierlich. Fragmentary 5S rRNA gene in the human mitochondrial genome , 1982, Molecular and cellular biology.
[19] S. Altman,et al. Characterization of an RNase P activity from HeLa cell mitochondria. Comparison with the cytosol RNase P activity. , 1985, The Journal of biological chemistry.
[20] F. Amalric,et al. Fractionation of mitochondrial RNA from HeLa cells by high-resolution electrophoresis under strongly denaturing conditions. , 1978, Journal of molecular biology.
[21] N. Bresolin,et al. In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria. , 1991, Molecular and cellular biology.
[22] T. Wong,et al. In vitro replication of human mitochondrial DNA: Accurate initiation at the origin of light-strand synthesis , 1985, Cell.
[23] E. Schon,et al. In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes , 1995, Molecular and cellular biology.
[24] William C. Copeland,et al. Cloning and characterization of the human mitochondrial DNA polymerase, DNA polymerase γ , 1996 .
[25] A. Weissbach,et al. DNA polymerase of mitochondria is a gamma-polymerase. , 1977, The Journal of biological chemistry.
[26] P. Pavco,et al. Structural and functional studies of the rat mitochondrial single strand DNA binding protein P16. , 1990, Archives of biochemistry and biophysics.
[27] J. Jaehning,et al. The yeast mitochondrial RNA polymerase specificity factor, MTF1, is similar to bacterial sigma factors. , 1991, The Journal of biological chemistry.
[28] R. Doolittle,et al. URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit. , 1986, Science.
[29] L. Spremulli,et al. Expression, Purification, and Mechanistic Studies of Bovine Mitochondrial Translational Initiation Factor 2 (*) , 1996, The Journal of Biological Chemistry.
[30] D. Chang,et al. A mammalian mitochondrial RNA processing activity contains nucleus-encoded RNA. , 1987, Science.
[31] M. Walberg,et al. Sequence and properties of the human KB cell and mouse L cell D-loop regions of mitochondrial DNA. , 1981, Nucleic acids research.
[32] M. Rocchi,et al. Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis. , 1995, Genomics.
[33] G. G. Stokes. "J." , 1890, The New Yale Book of Quotations.
[34] The mitochondrial tRNA(Leu)(UUR)) mutation in MELAS: a model for pathogenesis. , 1992, Biochimica et biophysica acta.
[35] P. Meltzer,et al. A PAC containing the human mitochondrial DNA polymerase gamma gene (POLG) maps to chromosome 15q25. , 1997, Genomics.
[36] D. A. Clayton,et al. Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion. , 1994, Biochemical and biophysical research communications.
[37] D. Bogenhagen,et al. Identification of a promoter for transcription of the heavy strand of human mtDNA: In vitro transcription and deletion mutagenesis , 1984, Cell.
[38] B. Séraphin,et al. Accurate Processing of a Eukaryotic Precursor Ribosomal RNA by Ribonuclease MRP in Vitro , 1996, Science.
[39] L. Spremulli,et al. Cloning and Sequence Analysis of the Human Mitochondrial Translational Initiation Factor 2 cDNA (*) , 1995, The Journal of Biological Chemistry.
[40] V. Tiranti,et al. Single-stranded-DNA-binding proteins from human mitochondria and Escherichia coli have analogous physicochemical properties. , 1994, European journal of biochemistry.
[41] D. Chang,et al. A novel endoribonuclease cleaves at a priming site of mouse mitochondrial DNA replication. , 1987, The EMBO journal.
[42] J. N. Topper,et al. Characterization of human MRP/Th RNA and its nuclear gene: full length MRP/Th RNA is an active endoribonuclease when assembled as an RNP. , 1990, Nucleic acids research.
[43] L. Spremulli,et al. Cloning, sequence analysis and expression of mammalian mitochondrial protein synthesis elongation factor Tu. , 1995, Biochimica et biophysica acta.
[44] D. A. Clayton,et al. Minor transcription initiation events indicate that both human mitochondrial promoters function bidirectionally , 1986, Molecular and cellular biology.
[45] S. Crews,et al. Failure to detect "cap" structures in mitochondrial DNA-coded poly(A)-containing RNA from HeLa cells. , 1978, Nucleic acids research.
[46] C. Kang,et al. A common core for binding single‐stranded DNA: structural comparison of the single‐stranded DNA‐binding proteins (SSB) from E. coli and human mitochondria , 1997, FEBS letters.
[47] M. Rocchi,et al. Cloning of human and rat cDNAs encoding the mitochondrial single-stranded DNA-binding protein (SSB). , 1993, Gene.
[48] D. Wallace,et al. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation , 1990, Cell.
[49] R. Wiesner,et al. Stoichiometry of mitochondrial transcripts and regulation of gene expression by mitochondrial transcription factor A. , 1994, Biochemical and biophysical research communications.
[50] F. Sanger,et al. Sequence and organization of the human mitochondrial genome , 1981, Nature.
[51] C. Merril,et al. Localization by fluorescence in situ hybridization (FISH) of human mitochondrial polymerase gamma (POLG) to human chromosome band 15q24-->q26, and of mouse mitochondrial polymerase gamma (Polg) to mouse chromosome band 7E, with confirmation by direct sequence analysis of bacterial artificial chromos , 1997, Cytogenetics and cell genetics.
[52] J. N. Topper,et al. Promoter selection in human mitochondria involves binding of a transcription factor to orientation-independent upstream regulatory elements , 1987, Cell.
[53] W. Filipowicz,et al. Evidence against a mitochondrial location of the 7-2/MRP RNA in mammalian cells , 1992, Cell.
[54] A. Lezza,et al. Synthesis and turnover rates of four rat liver mitochondrial RNA species , 1987, FEBS letters.
[55] L. Spremulli,et al. Bovine mitochondrial protein synthesis elongation factors. Identification and initial characterization of an elongation factor Tu-elongation factor Ts complex. , 1989, The Journal of biological chemistry.
[56] Apollonia Tullo,et al. Human Mitochondrial tRNA Processing (*) , 1995, The Journal of Biological Chemistry.
[57] R. Jensen,et al. Protein translocation across mitochondrial membranes: What a long, strange trip it is , 1995, Cell.
[58] S. Jacob,et al. Mitochondrial poly(A) polymerase from a poorly differentiated hepatoma: purification and characteristics. , 1975, Biochemistry.
[59] G. Attardi,et al. Evidence for complete symmetrical transcription in vivo of mitochondrial DNA in HeLa cells. , 1975, Journal of molecular biology.
[60] F. Foury,et al. Mitochondrial DNA polymerases from yeast to man: a new family of polymerases. , 1997, Gene.
[61] M W Gray,et al. The endosymbiont hypothesis revisited. , 1992, International review of cytology.
[62] K. Nierhaus. An elongation factor turn-on , 1996, Nature.
[63] J. Montoya,et al. Distinctive features of the 5′-terminal sequences of the human mitochondrial mRNAs , 1981, Nature.
[64] A. Harding,et al. A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies. , 1992, Brain : a journal of neurology.
[65] Ian G. Macreadie,et al. Biogenesis of mitochondria: the mitochondrial gene (aap1) coding for mitochondrial ATPase subunit 8 in Saccharomyces cerevisiae , 1983, Nucleic Acids Res..
[66] Y. Kagawa,et al. Upstream region of a genomic gene for human mitochondrial transcription factor 1. , 1992, Biochimica et biophysica acta.
[67] A. Duncan,et al. The human mitochondrial elongation factor tu (EF-Tu) gene: cDNA sequence, genomic localization, genomic structure, and identification of a pseudogene. , 1997, Gene.
[68] I. Antoshechkin,et al. Distinct roles for two purified factors in transcription of Xenopus mitochondrial DNA , 1995, Molecular and cellular biology.
[69] C. Hutchison,et al. Maternal inheritance of mammalian mitochondrial DNA , 1974, Nature.
[70] L. Spremulli,et al. Mechanistic studies of the translational elongation cycle in mammalian mitochondria. , 1997, Biochimica et biophysica acta.
[71] J. Richardson,et al. Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis , 1994, The Journal of cell biology.
[72] J. Diffley,et al. DNA binding properties of an HMG1-related protein from yeast mitochondria. , 1992, The Journal of biological chemistry.
[73] S. Love,et al. Liver failure associated with mitochondrial DNA depletion. , 1998, Journal of hepatology.
[74] R. Doolittle,et al. Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase , 1985, Nature.
[75] D. A. Clayton,et al. A tridecamer DNA sequence supports human mitochondrial RNA 3'-end formation in vitro , 1988, Molecular and Cellular Biology.
[76] J. Hixson,et al. Both the conserved stem-loop and divergent 5'-flanking sequences are required for initiation at the human mitochondrial origin of light-strand DNA replication. , 1986, The Journal of biological chemistry.
[77] F. Foury. Cloning and sequencing of the nuclear gene MIP1 encoding the catalytic subunit of the yeast mitochondrial DNA polymerase. , 1989, The Journal of biological chemistry.
[78] J. Paluh,et al. A functional dominant mutation in Schizosaccharomyces pombe RNase MRP RNA affects nuclear RNA processing and requires the mitochondrial‐associated nuclear mutation ptp1–1 for viability. , 1996, The EMBO journal.
[79] G. Attardi,et al. Markedly different ATP requirements for rRNA synthesis and mtDNA light strand transcription versus mRNA synthesis in isolated human mitochondria. , 1987, The Journal of biological chemistry.
[80] D. A. Clayton,et al. Replication and transcription of vertebrate mitochondrial DNA. , 1991, Annual review of cell biology.
[81] C. Moraes,et al. Functional and Molecular Mitochondrial Abnormalities Associated with a C T Transition at Position 3256 of the Human Mitochondrial Genome , 1996, The Journal of Biological Chemistry.
[82] S. Swoap,et al. Differential Expression of Mitochondrial DNA Replication Factors in Mammalian Tissues* , 1998, The Journal of Biological Chemistry.
[83] T. Wong,et al. Purification and identification of subunit structure of the human mitochondrial DNA polymerase. , 1992, The Journal of biological chemistry.
[84] R. Fisher,et al. A transcription factor required for promoter recognition by human mitochondrial RNA polymerase. Accurate initiation at the heavy- and light-strand promoters dissected and reconstituted in vitro. , 1985, The Journal of biological chemistry.
[85] M. Olson,et al. Subunit Structure of Mitochondrial DNA Polymerase from Drosophila Embryos , 1995, The Journal of Biological Chemistry.
[86] S. Dimauro,et al. Mitochondrial DNA and RNA processing in MELAS , 1996, Annals of neurology.
[87] D. Bogenhagen. Interaction of mtTFB and mtRNA polymerase at core promoters for transcription of Xenopus laevis mtDNA. , 1996, The Journal of biological chemistry.
[88] Y. Hatefi. The mitochondrial electron transport and oxidative phosphorylation system. , 1985, Annual review of biochemistry.
[89] M. Schmitt,et al. Yeast site-specific ribonucleoprotein endoribonuclease MRP contains an RNA component homologous to mammalian RNase MRP RNA and essential for cell viability. , 1992, Genes & development.
[90] D. A. Clayton,et al. RNA‐DNA hybrid formation at the human mitochondrial heavy‐strand origin ceases at replication start sites: an implication for RNA‐DNA hybrids serving as primers. , 1996, The EMBO journal.
[91] C. Moraes,et al. A disease-associated G5703A mutation in human mitochondrial DNA causes a conformational change and a marked decrease in steady-state levels of mitochondrial tRNA(Asn) , 1997, Molecular and cellular biology.
[92] J. Cote,et al. Primers for mitochondrial DNA replication generated by endonuclease G. , 1993, Science.
[93] E. Robin,et al. Mitochondrial DNA molecules and virtual number of mitochondria per cell in mammalian cells , 1988, Journal of cellular physiology.
[94] Julio Montoya,et al. tRNA punctuation model of RNA processing in human mitochondria , 1981, Nature.
[95] T. W. O'brien,et al. Protein composition of the bovine mitochondrial ribosome. , 1982, The Journal of biological chemistry.
[96] N. Martin,et al. Characterization of the yeast mitochondrial locus necessary for tRNA biosynthesis: DNA sequence analysis and identification of a new transcript , 1983, Cell.
[97] J. Cooper,et al. Respiratory-deficient human fibroblasts exhibiting defective mitochondrial DNA replication. , 1995, The Biochemical journal.
[98] G. Attardi,et al. Intercalating drugs and low temperatures inhibit synthesis and processing of ribosomal RNA in isolated human mitochondria. , 1984, Journal of molecular biology.
[99] D. Wallace,et al. Mitochondrial DNA in anucleate human blood cells. , 1988, Biochemical and biophysical research communications.
[100] V. Weissig,et al. Delayed cytotoxicity and cleavage of mitochondrial DNA in ciprofloxacin-treated mammalian cells. , 1996, Molecular pharmacology.
[101] W. D. de Vos,et al. The heterogeneity of rat-liver mitochondrial DNA. , 1978, Biochimica et biophysica acta.
[102] E. Schon,et al. Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. , 1992, Molecular and cellular biology.
[103] J. Cooper,et al. Nuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion. , 1993, American journal of human genetics.
[104] J. Maassen,et al. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness , 1992, Nature Genetics.
[105] L. Spremulli,et al. Cloning and Expression of Mitochondrial Translational Elongation Factor Ts from Bovine and Human Liver (*) , 1995, The Journal of Biological Chemistry.
[106] G. Soslau,et al. Immunological identification of human platelet mitochondrial DNA topoisomerase I. , 1993, Biochimica et biophysica acta.
[107] V. Tiranti,et al. Characterization and expression of the mouse endonuclease G gene. , 1997, DNA and cell biology.
[108] S. Dimauro,et al. Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region , 1991, Molecular and cellular biology.
[109] T. Wong,et al. DNA primase of human mitochondria is associated with structural RNA that is essential for enzymatic activity , 1986, Cell.
[110] Galper Jb,et al. The presence of N-formyl-methionyl-tRNA in HeLa cell mitochondria. , 1969 .
[111] D. A. Clayton,et al. Mechanism of replication of human mitochondrial DNA. Localization of the 5' ends of nascent daughter strands. , 1981, The Journal of biological chemistry.
[112] J. N. Topper,et al. A role for RNAse MRP in mitochondrial RNA processing , 1992, Cell.
[113] D. Bogenhagen,et al. Identification and in vitro capping of a primary transcript of human mitochondrial DNA. , 1984, The Journal of biological chemistry.
[114] K. Komori,et al. Cloning and characterization of the gene encoding a mitochondrially localized DNA topoisomerase II in Dictyostelium discoideum. Western blot analysis. , 1997, Biochimica et biophysica acta.
[115] D. A. Clayton,et al. Similarity of human mitochondrial transcription factor 1 to high mobility group proteins. , 1991, Science.
[116] H. P. Zassenhaus,et al. Construction of a yeast mutant lacking the mitochondrial nuclease. , 1988, Nucleic acids research.
[117] L. Spremulli,et al. Initiation of protein synthesis in animal mitochondria. Purification and characterization of translational initiation factor 2. , 1991, The Journal of biological chemistry.
[118] D. Clayton,et al. Mechanism of mitochondrial DNA replication in mouse L-cells: localization and sequence of the light-strand origin of replication. , 1979, Journal of molecular biology.
[119] G. Attardi,et al. Termination of transcription in human mitochondria: Identification and purification of a DNA binding protein factor that promotes termination , 1989, Cell.
[120] L. Defrancesco,et al. In situ photochemical crosslinking of HeLa cell mitochondrial DNA by a psoralen derivative reveals a protected region near the origin of replication. , 1981, Nucleic acids research.
[121] E. Shoubridge,et al. Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF). , 1992, American journal of human genetics.
[122] D. Lee,et al. RNase mitochondrial RNA processing correctly cleaves a novel R loop at the mitochondrial DNA leading-strand origin of replication. , 1997, Genes & development.
[123] P. Fernández-Silva,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 , 1997, The EMBO journal.
[124] T. W. O'brien,et al. Ultracentrifugal characterization of the mitochondrial ribosome and subribosomal particles of bovine liver: molecular size and composition. , 1974, Biochemistry.
[125] Miss A.O. Penney. (b) , 1974, The New Yale Book of Quotations.
[126] M. Rocchi,et al. Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags database. , 1997, Human molecular genetics.
[127] L. Spremulli,et al. Interaction of bovine mitochondrial ribosomes with messenger RNA. , 1989, The Journal of biological chemistry.
[128] J. Cooper,et al. Molecular mechanisms in mitochondrial DNA depletion syndrome. , 1997, Human molecular genetics.
[129] S. Ho,et al. Maternal inheritance of the mouse mitochondrial genome is not mediated by a loss or gross alteration of the paternal mitochondrial DNA or by methylation of the oocyte mitochondrial DNA. , 1984, Developmental biology.
[130] Y. Mechulam,et al. Molecular recognition governing the initiation of translation in Escherichia coli. A review. , 1996, Biochimie.
[131] D. A. Clayton,et al. Purification and characterization of human mitochondrial transcription factor 1 , 1988, Molecular and cellular biology.
[132] W. Hauswirth,et al. Mitochondrial DNA copy number in bovine oocytes and somatic cells. , 1982, Developmental biology.
[133] G. Barsh,et al. Down-regulation of mitochondrial transcription factor A during spermatogenesis in humans. , 1997, Human molecular genetics.
[134] M. Parisi,et al. DNA wrapping and bending by a mitochondrial high mobility group-like transcriptional activator protein. , 1992, The Journal of biological chemistry.
[135] R. Aebersold,et al. Molecular characterization of the transcription termination factor from human mitochondria. , 1993, The Journal of biological chemistry.
[136] O. Cummings,et al. Purification and characterization of the potent endonuclease in extracts of bovine heart mitochondria. , 1987, The Journal of biological chemistry.
[137] J. Montoya,et al. Sequence analysis and precise mapping of the 3' ends of HeLa cell mitochondrial ribosomal RNAs. , 1982, Journal of molecular biology.
[138] D. A. Clayton,et al. Human mitochondrial transcription termination exhibits RNA polymerase independence and biased bipolarity in vitro. , 1994, The Journal of biological chemistry.
[139] Eukaryotic DNA polymerases. , 1991, Annual review of biochemistry.
[140] G. Shadel,et al. Mitochondrial DNA maintenance in vertebrates. , 1997, Annual review of biochemistry.
[141] J. Enríquez,et al. MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNALys and premature translation termination , 1995, Nature Genetics.
[142] I. Antoshechkin,et al. The HMG‐box mitochondrial transcription factor xl‐mtTFA binds DNA as a tetramer to activate bidirectional transcription , 1997, The EMBO journal.
[143] C. G. Edmonds,et al. 5-[[(carboxymethyl)amino]methyl]uridine is found in the anticodon of yeast mitochondrial tRNAs recognizing two-codon families ending in a purine. , 1990, Biochemistry.
[144] F. Castora,et al. Search for a DNA gyrase in mammalian mitochondria. , 1979, The Journal of biological chemistry.
[145] M. Roberti,et al. Multiple protein-binding sites in the TAS-region of human and rat mitochondrial DNA. , 1998, Biochemical and biophysical research communications.
[146] J. Montoya,et al. The pattern of transcription of the human mitochondrial rRNA genes reveals two overlapping transcription units , 1983, Cell.
[147] Mariana Gerschenson,et al. Endonuclease G from mammalian nuclei is identical to the major endonuclease of mitochondria , 1995, Nucleic Acids Res..
[148] M. Walberg,et al. In vitro transcription of human mitochondrial DNA. Identification of specific light strand transcripts from the displacement loop region. , 1983, The Journal of biological chemistry.
[149] G. Soslau,et al. Mitochondrial DNA topoisomerase I from human platelets. , 1991, Biochimica et biophysica acta.
[150] M. Parisi,et al. Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies , 1991, Nature.
[151] R Grosschedl,et al. HMG domain proteins: architectural elements in the assembly of nucleoprotein structures. , 1994, Trends in genetics : TIG.
[152] R. Wiesner,et al. Counting target molecules by exponential polymerase chain reaction: copy number of mitochondrial DNA in rat tissues. , 1992, Biochemical and biophysical research communications.
[153] I. Nonaka,et al. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies , 1990, Nature.
[154] G. Schatten,et al. Fate of the sperm mitochondria, and the incorporation, conversion, and disassembly of the sperm tail structures during bovine fertilization. , 1996, Biology of reproduction.
[155] J. Carrodeguas,et al. The γ Subfamily of DNA Polymerases: Cloning of a Developmentally Regulated cDNA Encoding Xenopus Laevis Mitochondrial DNA Polymerase γ , 1996 .
[156] G. Barsh,et al. Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice , 1998, Nature Genetics.
[157] D. A. Clayton,et al. Identification of transcriptional regulatory elements in human mitochondrial DNA by linker substitution analysis , 1989, Molecular and cellular biology.
[158] A. Williams,et al. Stimulation of Drosophila Mitochondrial DNA Polymerase by Single-stranded DNA-binding Protein (*) , 1995, The Journal of Biological Chemistry.
[159] G. Michaels,et al. Mechanism of mRNA binding to bovine mitochondrial ribosomes. , 1989, The Journal of biological chemistry.
[160] D. A. Clayton,et al. A single mouse gene encodes the mitochondrial transcription factor A and a testis–specific nuclear HMG-box protein , 1996, Nature Genetics.
[161] D. A. Clayton,et al. Addition of a 29 residue carboxyl-terminal tail converts a simple HMG box-containing protein into a transcriptional activator. , 1995, Journal of molecular biology.
[162] D. Wolstenholme,et al. Animal mitochondrial DNA: structure and evolution. , 1992, International review of cytology.
[163] W. Hauswirth,et al. Replication priming and transcription initiate from precisely the same site in mouse mitochondrial DNA. , 1985, The EMBO journal.
[164] F. Castora,et al. The presence of two mitochondrial DNA topoisomerases in human acute leukemia cells. , 1985, Biochemical and biophysical research communications.
[165] A. Tua,et al. Mitochondrial DNA topoisomerase I of Saccharomyces cerevisiae. , 1997, Biochimie.
[166] S. Graves,et al. Expression, purification, and initial kinetic characterization of the large subunit of the human mitochondrial DNA polymerase. , 1998, Biochemistry.
[167] M. Leversha,et al. A mitochondrial elongation factor‐like protein is over‐expressed in tumours and differentially expressed in normal tissues , 1995, FEBS letters.
[168] B. Wittmann-Liebold,et al. Mitochondrial ribosomal proteins (MRPs) of yeast. , 1998, The Biochemical journal.
[169] T. Lisowsky,et al. A rapid, efficient method for purifying DNA-binding proteins. Denaturation-renaturation chromatography of human and yeast mitochondrial extracts. , 1991, The Journal of biological chemistry.
[170] S. Dimauro,et al. The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle. , 1992, American journal of human genetics.
[171] F. Foury,et al. A single‐stranded DNA binding protein required for mitochondrial DNA replication in S. cerevisiae is homologous to E. coli SSB. , 1992, The EMBO journal.
[172] E. Schon,et al. Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS. , 1993, Nucleic acids research.
[173] L. Spremulli,et al. Cloning and sequence analysis of the cDNA for bovine mitochondrial translational initiation factor 2. , 1995, Biochimica et biophysica acta.
[174] M. Roberti,et al. DNA-helicase activity from sea urchin mitochondria. , 1996, Biochemical and biophysical research communications.
[175] P. Fernández-Silva,et al. Functional Analysis of in Vivo and in Organello Footprinting of HeLa Cell Mitochondrial DNA in Relationship to ATP and Ethidium Bromide Effects on Transcription* , 1997, The Journal of Biological Chemistry.
[176] D A Clayton,et al. Nuclear RNase MRP is required for correct processing of pre-5.8S rRNA in Saccharomyces cerevisiae , 1993, Molecular and cellular biology.
[177] D. A. Clayton,et al. Mitochondrial transcription initiation. Variation and conservation. , 1993, The Journal of biological chemistry.
[178] D. A. Clayton,et al. Replication of animal mitochondrial DNA , 1982, Cell.
[179] W. Copeland,et al. Mitochondrial DNA polymerase gamma is expressed and translated in the absence of mitochondrial DNA maintenance and replication. , 1996, Nucleic Acids Research.
[180] D. A. Clayton,et al. Identification of the 3'-ends of the two mouse mitochondrial ribosomal RNAs. The 3'-end of 16 S ribosomal RNA contains nucleotides encoded by the gene for transfer RNALeuUUR. , 1983, The Journal of biological chemistry.
[181] D. Chang,et al. Precise identification of individual promoters for transcription of each strand of human mitochondrial DNA , 1984, Cell.
[182] W. Hauswirth,et al. In organello footprint analysis of human mitochondrial DNA: human mitochondrial transcription factor A interactions at the origin of replication , 1994, Molecular and cellular biology.
[183] L. Pikó,et al. Number of mitochondria and some properties of mitochondrial DNA in the mouse egg. , 1976, Developmental biology.
[184] G. Shadel,et al. Human mitochondrial transcription factor A and promoter spacing integrity are required for transcription initiation. , 1995, Biochimica et biophysica acta.
[185] E. Schon,et al. The fate of human sperm-derived mtDNA in somatic cells. , 1997, American journal of human genetics.