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Mito Communication

Genetic diversities of MT-ND3 and MT-ND4L genes are associated with high-altitude adaptation

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Pages 324-328 | Received 05 Aug 2018, Accepted 20 Oct 2018, Published online: 28 Dec 2018

References

  • Adam MP, Ardinger HH, Pagon RA, Wallace SE, Ljh B, Stephens K, Amemiya A. 2003. Mitochondrial DNA-associated Leigh syndrome and NARP: PubMed.
  • Chandel NS, Maltepe E, Goldwasser E, Mathieu CE, Simon MC, Schumacker PT. 1998. Mitochondrial reactive oxygen species trigger hypoxia-induced transcription. Proc Natl Acad Sci U S A. 95:11715–11720.
  • Consortium UP. 2015. UniProt: a hub for protein information. Nucl Acids Res. 43:204–212.
  • Coskun PE, Ruiz-Pesini E, Wallace DC. 2003. Control region mtDNA variants: longevity, climatic adaptation, and a forensic conundrum. Proc Natl Acad Sci U S A. 100:2174.
  • Flaquer A, Baumbach C, Kriebel J, Meitinger T, Peters A, Waldenberger M, Grallert H, Strauch K. 2014. Mitochondrial genetic variants identified to be associated with BMI in adults. PLoS One. 9:e105116.
  • Ghezzi D, Marelli C, Achilli A, Goldwurm S, Pezzoli G, Barone P, Pellecchia MT, Stanzione P, Brusa L, Bentivoglio AR, et al. 2005. Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians. Eur J Hum Genet. 13:748.
  • Gnaiger E. 2003. Oxygen conformance of cellular respiration. Hypoxia. Springer; p. 39–55.
  • Harri R, Johanna A, Heli YO, Aino L, Juha P, Hassinen IE, Kari M. 2002. Cytoskeletal structure of myoblasts with the mitochondrial DNA 3243Asn Italiansisease in Italiansame> <fname > E.</fname> <sname > Ruiz-Pesini<. Cell Motil Cytoskeleton. 53:231–238.
  • La MC, Caporali L, Gandini F, Olivieri A, Toni F, Nassetti S, Brunetto D, Stipa C, Scaduto C, Parmeggiani A. 2014. Association of the mtDNA m.4171C > A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions. BMC Neurol. 14:1–5.
  • Leonard JV, Schapira A. 2000. Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects. Lancet. 355:389.
  • Luo Y, Gao W, Gao Y, Tang S, Huang Q, Tan X, Chen J, Huang T. 2008. Mitochondrial genome analysis of Ochotona curzoniae and implication of cytochrome c oxidase in hypoxic adaptation. Mitochondrion. 8:352–357.
  • Mishmar D, Ruiz-Pesini E, Golik P, Macaulay V, Clark AG, Hosseini S, Brandon M, Easley K, Chen E, Brown MD, et al. 2003. Natural selection shaped regional mtDNA variation in humans. Proc Natl Acad Sci USA. 100:171–176.
  • Mukai M, Sugaya K, Ozawa T, Goto YI, Yagishita A, Matsubara S, Bokuda K, Miyakoshi A, Nakano I. 2015. Isolated mitochondrial stroke‐like episodes in an elderly patient with the MT‐ND3 gene mutation. Neurol Clin Neurosci. 3:153–156.
  • Nakamaru-Ogiso E, Han H, Matsuno-Yagi A, Keinan E, Sinha SC, Yagi T, Ohnishi T. 2010. The ND2 subunit is labeled by a photoaffinity analogue of asimicin, a potent complex I inhibitor. FEBS Lett. 584:883–888.
  • Nesbitt V, Morrison PJ, Crushell E, Donnelly DE, Alston CL, He L, McFarland R, Taylor RW. 2012. The clinical spectrum of the m.10191T > C mutation in complex I-deficient Leigh syndrome. Dev Med Child Neurol. 54:500–506.
  • Newman JH, Holt TN, Hedges LK, Womack B, Memon SS, Willers ED, Wheeler L, Phillips JA, Hamid R. 2011. High-altitude pulmonary hypertension in cattle (brisket disease): candidate genes and gene expression profiling of peripheral blood mononuclear cells. Pulmonary Circulation. 1:462–469.
  • Reed KL, Blaeser LL, Dantzer V, Green ML, Simmen RC. 1998. Control of secretory leukocyte protease inhibitor gene expression in the porcine periimplantation endometrium: a case of maternal-embryo communication. Biol Reprod. 58:448.
  • Sarzi E, Brown MD, Lebon S, Chretien D, Munnich A, Rotig A, Procaccio V. 2007. A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia. Am J Med Genet A. 143A:33–41.
  • Scott GR, Schulte PM, Egginton S, Scott ALM, Richards JG, Milsom WK. 2011. Molecular evolution of cytochrome c oxidase underlies high-altitude adaptation in the bar-headed goose. molecular. Biol Evol. 28:351.
  • Shi Y, Hu Y, Wang J, Elzo MA, Yang X, Lai S. 2018. Genetic diversities of MT-ND1 and MT-ND2 genes are associated with high-altitude adaptation in yak. Mitochondrial DNA Part A. 29:485–494.
  • Wang HN, Chen HD, Chen KY, Xiao JF, He K, Xiang GA, Xie X. 2014. Highly expressed MT-ND3 positively associated with histological severity of hepatic steatosis. APMIS. 122:443–451.
  • Weir EK, Tucker A, Reeves JT, Will DH, Grover RF. 1974. The genetic factor influencing pulmonary hypertension in cattle at high altitude. Cardiovasc Res. 8:745–749.
  • Yan-Iing Zhao, Jian-Zhou Wang, Yang-Zom Y-X. 2011. Isolation and culture of fetal fibroblasts of Tibetan yellow cattle. Animal Husbandry Feed Sci. 10:3–5.
  • Yu WMP, Turnbull DM, Chinnery PF. 2005. Leber hereditary optic neuropathy. Berlin, Heidelberg: Springer.