MTERF3 Is a Negative Regulator of Mammalian mtDNA Transcription
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H. Erdjument-Bromage | P. Tempst | C. Gustafsson | M. Falkenberg | N. Larsson | Yonghong Shi | K. Hultenby | R. Wibom | Chan Bae Park | M. Gaspari | Y. Cámara | Mina Pellegrini | J. Asin-Cayuela
[1] M. Beal,et al. Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases , 2006, Nature.
[2] C. Manzari,et al. MTERF3, the most conserved member of the mTERF-family, is a modular factor involved in mitochondrial protein synthesis. , 2006, Biochimica et biophysica acta.
[3] A. Trifunovic. Mitochondrial DNA and ageing. , 2006, Biochimica et biophysica acta.
[4] R. Scarpulla,et al. Nuclear control of respiratory gene expression in mammalian cells , 2006, Journal of cellular biochemistry.
[5] J. Griffith,et al. Termination Factor-Mediated DNA Loop between Termination and Initiation Sites Drives Mitochondrial rRNA Synthesis , 2005, Cell.
[6] T. Samuelsson,et al. A family of putative transcription termination factors shared amongst metazoans and plants , 2005, Current Genetics.
[7] C. Gustafsson,et al. The Human Mitochondrial Transcription Termination Factor (mTERF) Is Fully Active in Vitro in the Non-phosphorylated Form* , 2005, Journal of Biological Chemistry.
[8] A. Trifunovic,et al. Mitochondrial DNA polymerase gamma is essential for mammalian embryogenesis. , 2005, Human molecular genetics.
[9] Christoph Handschin,et al. Metabolic control through the PGC-1 family of transcription coactivators. , 2005, Cell metabolism.
[10] C. Gustafsson,et al. The mitochondrial RNA polymerase contributes critically to promoter specificity in mammalian cells , 2004, The EMBO journal.
[11] Jiandie D. Lin,et al. Defects in Adaptive Energy Metabolism with CNS-Linked Hyperactivity in PGC-1α Null Mice , 2004, Cell.
[12] Howard T. Jacobs,et al. Premature ageing in mice expressing defective mitochondrial DNA polymerase , 2004, Nature.
[13] Kjell Hultenby,et al. Mitochondrial transcription factor A regulates mtDNA copy number in mammals. , 2004, Human molecular genetics.
[14] E. Dufour,et al. A switch in metabolism precedes increased mitochondrial biogenesis in respiratory chain-deficient mouse hearts. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[15] 古賀 敦子. Increased mitochondrial processing intermediates associated with three tRNA[Leu(UUR)] gene mutations , 2004 .
[16] T. Matsuishi,et al. Increased mitochondrial processing intermediates associated with three tRNALeu(UUR) gene mutations , 2003, Neuromuscular Disorders.
[17] G. Shadel,et al. Human mitochondrial transcription factor B1 methylates ribosomal RNA at a conserved stem-loop , 2003, Nature Genetics.
[18] L. Hagenfeldt,et al. Measurement of ATP production and respiratory chain enzyme activities in mitochondria isolated from small muscle biopsy samples. , 2002, Analytical biochemistry.
[19] H. Westerblad,et al. Increased mitochondrial mass in mitochondrial myopathy mice , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[20] N. Proudfoot,et al. Transcriptional collision between convergent genes in budding yeast , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[21] C. Gustafsson,et al. Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA , 2002, Nature Genetics.
[22] S. Dimauro,et al. The genetics and pathology of oxidative phosphorylation , 2001, Nature Reviews Genetics.
[23] D. Court,et al. A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA. , 2001, Genomics.
[24] Reynaldo Sequerra,et al. High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP , 2000, Nature Genetics.
[25] H. Li,et al. Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[26] V. Mootha,et al. Mechanisms Controlling Mitochondrial Biogenesis and Respiration through the Thermogenic Coactivator PGC-1 , 1999, Cell.
[27] Jens C. Brüning,et al. Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression , 1999, Nature Genetics.
[28] G. Barsh,et al. Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice , 1998, Nature Genetics.
[29] 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.
[30] P. Fernández-Silva,et al. Isolation and assay of mitochondrial transcription termination factor from human cells. , 1996, Methods in enzymology.
[31] J. Enríquez,et al. In organello RNA synthesis system from mammalian liver and brain. , 1996, Methods in enzymology.
[32] 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.
[33] D. A. Clayton,et al. Human mitochondrial transcription termination exhibits RNA polymerase independence and biased bipolarity in vitro. , 1994, The Journal of biological chemistry.
[34] H. Erdjument-Bromage,et al. Improvements in Microsequencer Performance for Low Picomole Sequence Analysis , 1994 .
[35] D. Turnbull,et al. Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA. A potential disease mechanism. , 1993, The Journal of biological chemistry.
[36] D. Wallace,et al. Mitochondrial DNA expression in mitochondrial myopathies and coordinated expression of nuclear genes involved in ATP production. , 1993, The Journal of biological chemistry.
[37] H. Schägger,et al. Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form. , 1991, Analytical biochemistry.
[38] J. Hayashi,et al. Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[39] D. A. Clayton,et al. Similarity of human mitochondrial transcription factor 1 to high mobility group proteins. , 1991, Science.
[40] J. Carey. [8] Gel retardation , 1991 .
[41] J. Carey. Gel retardation. , 1991, Methods in enzymology.
[42] G. Attardi,et al. Termination of transcription in human mitochondria: Identification and purification of a DNA binding protein factor that promotes termination , 1989, Cell.
[43] R. Knippers,et al. DNA Polymerase II , 1970, Nature.