Mitochondrial DNA replication and OXPHOS gene transcription show varied responsiveness to Rieske protein knockdown in 143B cells.
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F. H. van der Westhuizen | J. Smeitink | L. Nijtmans | R. Louw | L. D. du Plessis | P. J. Pretorius | O. Levanets | F. Reinecke
[1] T. Gabaldón,et al. Impact of the Mitochondrial Genetic Background in Complex III Deficiency , 2010, PloS one.
[2] S. Seneca,et al. Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency , 2010, Human mutation.
[3] F. H. van der Westhuizen,et al. OXPHOS genes expression and control in mitochondrial disorders , 2020 .
[4] M. Roberti,et al. Nuclear Respiratory Factor 2 Induces the Expression of Many but Not All Human Proteins Acting in Mitochondrial DNA Transcription and Replication* , 2009, The Journal of Biological Chemistry.
[5] D. Smiraglia,et al. A novel role for mitochondria in regulating epigenetic modifications in the nucleus , 2008, Cancer biology & therapy.
[6] U. Brandt,et al. The Mechanism of Mitochondrial Superoxide Production by the Cytochrome bc1 Complex* , 2008, Journal of Biological Chemistry.
[7] G. Shadel. Expression and maintenance of mitochondrial DNA: new insights into human disease pathology. , 2008, The American journal of pathology.
[8] C. Moraes,et al. Transcriptional co-expression and co-regulation of genes coding for components of the oxidative phosphorylation system , 2008, BMC Genomics.
[9] J. Smeitink,et al. Mitochondrial and cytosolic thiol redox state are not detectably altered in isolated human NADH:ubiquinone oxidoreductase deficiency. , 2007, Biochimica et biophysica acta.
[10] J. Smeitink,et al. Human NADH:ubiquinone oxidoreductase deficiency: radical changes in mitochondrial morphology? , 2007, American journal of physiology. Cell physiology.
[11] C. Gustafsson,et al. DNA replication and transcription in mammalian mitochondria. , 2007, Annual review of biochemistry.
[12] J. Eisenbart,et al. Jcb: Article , 2022 .
[13] G. Semenza,et al. HIF-1 Regulates Cytochrome Oxidase Subunits to Optimize Efficiency of Respiration in Hypoxic Cells , 2007, Cell.
[14] C. Gustafsson,et al. Mitochondrial transcription and its regulation in mammalian cells. , 2007, Trends in biochemical sciences.
[15] J. Smeitink,et al. Superoxide production is inversely related to complex I activity in inherited complex I deficiency. , 2007, Biochimica et biophysica acta.
[16] J. Hayashi,et al. Respiratory chain deficiency slows down cell‐cycle progression via reduced ROS generation and is associated with a reduction of p21CIP1/WAF1 , 2006, Journal of cellular physiology.
[17] W. C. Chan,et al. PCR-based generation of shRNA libraries from cDNAs , 2006, BMC biotechnology.
[18] A. Olckers,et al. Metallothionein isoform 2A expression is inducible and protects against ROS-mediated cell death in rotenone-treated HeLa cells. , 2006, The Biochemical journal.
[19] V. Petruzzella,et al. Dysfunctions of Cellular Oxidative Metabolism in Patients with Mutations in the NDUFS1 and NDUFS4 Genes of Complex I* , 2006, Journal of Biological Chemistry.
[20] Pierre Lescuyer,et al. Alterations of the mitochondrial proteome caused by the absence of mitochondrial DNA: A proteomic view , 2006, Electrophoresis.
[21] C. Piantadosi,et al. Mitochondrial Transcription Factor A Induction by Redox Activation of Nuclear Respiratory Factor 1* , 2006, Journal of Biological Chemistry.
[22] E. García-Arumí,et al. Enhanced ROS production and antioxidant defenses in cybrids harbouring mutations in mtDNA , 2006, Neuroscience Letters.
[23] Massimo Zeviani,et al. Mitochondrial medicine: a metabolic perspective on the pathology of oxidative phosphorylation disorders. , 2006, Cell metabolism.
[24] Massimo Zeviani,et al. Oxygen sensing requires mitochondrial ROS but not oxidative phosphorylation. , 2005, Cell metabolism.
[25] Yau-Huei Wei,et al. Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress. , 2005, The international journal of biochemistry & cell biology.
[26] F. Muller,et al. Complex III Releases Superoxide to Both Sides of the Inner Mitochondrial Membrane* , 2004, Journal of Biological Chemistry.
[27] Rutger O. Vogel,et al. Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies. , 2004, Human molecular genetics.
[28] P. Brookes,et al. Calcium, ATP, and ROS: a mitochondrial love-hate triangle. , 2004, American journal of physiology. Cell physiology.
[29] H. C. Lee,et al. Alteration of the copy number and deletion of mitochondrial DNA in human hepatocellular carcinoma , 2004, British Journal of Cancer.
[30] Kjell Hultenby,et al. Mitochondrial transcription factor A regulates mtDNA copy number in mammals. , 2004, Human molecular genetics.
[31] J. Smeitink,et al. Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency. , 2004, Human molecular genetics.
[32] W. Siegert,et al. Guideline to reference gene selection for quantitative real-time PCR. , 2004, Biochemical and biophysical research communications.
[33] K. Majamaa,et al. Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene , 2003, Annals of neurology.
[34] J. Hirst,et al. The nuclear encoded subunits of complex I from bovine heart mitochondria. , 2003, Biochimica et biophysica acta.
[35] B. Trumpower,et al. Protonmotive pathways and mechanisms in the cytochrome bc 1 complex , 2003, FEBS letters.
[36] R. Pfundt,et al. Human mitochondrial complex I deficiency: investigating transcriptional responses by microarray. , 2003, Neuropediatrics.
[37] B. Mousson de Camaret,et al. Large functional range of steady-state levels of nuclear and mitochondrial transcripts coding for the subunits of the human mitochondrial OXPHOS system. , 2002, Genome research.
[38] G. Shadel,et al. Modulation of mitochondrial transcription in response to mtDNA depletion and repletion in HeLa cells. , 2002, Nucleic acids research.
[39] G. Horgan,et al. Relative expression software tool (REST©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR , 2002 .
[40] N. Henderson,et al. Blue Native electrophoresis to study mitochondrial and other protein complexes. , 2002, Methods.
[41] Douglas C. Wallace,et al. Coordinate Induction of Energy Gene Expression in Tissues of Mitochondrial Disease Patients* , 1999, The Journal of Biological Chemistry.
[42] F. Leighton,et al. Oxidative stress and upregulation of mitochondrial biogenesis genes in mitochondrial DNA-depleted HeLa cells. , 1999, Biochemical and biophysical research communications.
[43] S. Swoap,et al. Differential Expression of Mitochondrial DNA Replication Factors in Mammalian Tissues* , 1998, The Journal of Biological Chemistry.
[44] J. L. Smith,et al. Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mtDNA depletion syndrome. , 1997, Biochimica et biophysica acta.
[45] 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.
[46] J. Christodoulou,et al. Leigh syndrome: Clinical features and biochemical and DNA abnormalities , 1996, Annals of neurology.
[47] R. Scarpulla,et al. Activation of the human mitochondrial transcription factor A gene by nuclear respiratory factors: a potential regulatory link between nuclear and mitochondrial gene expression in organelle biogenesis. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[48] 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.
[49] P. K. Smith,et al. Measurement of protein using bicinchoninic acid. , 1985, Analytical biochemistry.
[50] P. Garland,et al. The kinetic properties of citrate synthase from rat liver mitochondria. , 1969, The Biochemical journal.
[51] T. Puck,et al. A RAPID METHOD FOR VIABLE CELL TITRATION AND CLONE PRODUCTION WITH HELA CELLS IN TISSUE CULTURE: THE USE OF X-IRRADIATED CELLS TO SUPPLY CONDITIONING FACTORS. , 1955, Proceedings of the National Academy of Sciences of the United States of America.