Variations in mitochondrial tRNA^Thr gene may not be associated with coronary heart disease

References

• Chen B, Sun D, Yang L, Zhang C, Yang A, Zhu Y, Zhao J, et al. (2008). Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees. Am J Med Genet A 146A:1248–58
   PubMed Web of Science ®Google Scholar
• Davidson SM, Duchen MR. (2007). Endothelial mitochondria: Contributing to vascular function and disease. Circ Res 100:1128–41
   PubMed Web of Science ®Google Scholar
• DiMauro S. (2010). Pathogenesis and treatment of mitochondrial myopathies: Recent advances. Acta Myol 29:333–8
   PubMedGoogle Scholar
• Ding Y, Leng J. (2012). Is mitochondrial tRNA Leu(UUR) 3291T>C mutation pathogenic? Mitochondrial DNA 23:323–6
   Google Scholar
• Ding Y, Xia B, Yu J, Leng J, Huang J. (2013). Mitochondrial DNA mutations and essential hypertension (Review). Int J Mol Med 32:768–74
   PubMed Web of Science ®Google Scholar
• Florentz C, Sohm B, Tryoen-Toth P, Pütz J, Sissler M. (2003). Human mitochondrial tRNAs in health and disease. Cell Mol Life Sci 60:1356–75
   PubMed Web of Science ®Google Scholar
• Helm M, Brulé H, Friede D, Giegé R, Pütz D, Florentz C. (2000). Search for characteristic structural features of mammalian mitochondrial tRNAs. RNA 6:1356–79
   PubMed Web of Science ®Google Scholar
• Jin Y, Yu Q, Zhou D, Chen L, Huang X, Xu G, Huang J, et al. (2012). The mitochondrial DNA 9-bp deletion polymorphism is a risk factor for hepatocellular carcinoma in the Chinese population. Genet Test Mol Biomarkers 16:330–4
   PubMed Web of Science ®Google Scholar
• Li H, Liu D, Lu J, Bai Y. (2012). Physiology and pathophysiology of mitochondrial DNA. Adv Exp Med Biol 942:39–51
   PubMed Web of Science ®Google Scholar
• Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJ. (2006). Global and regional burden of disease and risk factors, 2001: Systematic analysis of population health data. Lancet 367:1747–57
   PubMed Web of Science ®Google Scholar
• Lu J, Sharma LK, Bai Y. (2009). Implications of mitochondrial DNA mutations and mitochondrial dysfunction in tumorigenesis. Cell Res 19:802–15
   PubMed Web of Science ®Google Scholar
• Qin Y, Xue L, Jiang P, Xu M, He Y, Shi S, Huang Y, et al. (2014). Mitochondrial tRNA variants in Chinese subjects with coronary heart disease. J Am Heart Assoc 3:e000437
   PubMed Web of Science ®Google Scholar
• Qu J, Zhou X, Zhao F, Liu X, Zhang M, Sun YH, Liang M, et al. (2010). Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation. Biochim Biophys Acta 1800:305–12
   PubMed Web of Science ®Google Scholar
• Qu J, Zhou X, Zhang J, Zhao F, Sun YH, Tong Y, Wei QP, et al. (2009). Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation. Ophthalmology 116:558–64
   PubMed Web of Science ®Google Scholar
• Rossmanith W, Karwan R. (1998). Impairment of tRNA processing by point mutations in mitochondrial tRNALeu(UUR) associated with mitochondrial diseases. FEBS Lett 433:269–74
   PubMed Web of Science ®Google Scholar
• Tuppen HA, Blakely EL, Turnbull DM, Taylor RW. (2010). Mitochondrial DNA mutations and human disease. Biochim Biophys Acta 1797:113–28
   PubMed Web of Science ®Google Scholar
• Wallace DC. (2010). Mitochondrial DNA mutations in disease and aging. Environ Mol Mutagen 51:440–50
   PubMed Web of Science ®Google Scholar
• Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, Chen B, et al. (2008). Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families. Pharmacogenet Genomics 18:1059–70
   PubMed Web of Science ®Google Scholar
• Wang Y, Dong P, Li L, Li X, Wang H, Yang X, Wang S, et al. (2014). The mitochondrial tRNAMet 4454T>C variant may not be associated with essential hypertension in Han Chinese population. Mitochondrial DNA 25:124--5
   Google Scholar
• Yasukawa T, Suzuki T, Suzuki T, Ueda T, Ohta S, Watanabe K. (2000). Modification defect at anticodon wobble nucleotide of mitochondrial tRNAsLeu(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. J Biol Chem 275:4251–7
   PubMed Web of Science ®Google Scholar
• Zhang XH, Lu ZL, Liu L. (2008). Coronary heart disease in China. Heart 94:1126–31
   PubMed Web of Science ®Google Scholar
• Zhou L, Wang H, Wei J, Wang Y, Wang Y. (2013). No association between mitochondrial tRNAVal T1658C mutation and chronic progressive external ophthalmoplegia (CPEO). Mitochondrial DNA Jul 2. [Epub ahead of print]. doi: 10.3109/19401736.2013.803097
   Google Scholar
• Zhu Q, Zhou Y, Jin X, Lin X. (2013). The role of mitochondrial tRNAPhe C628T variant in deafness expression. Mitochondrial DNA Sep 11. [Epub ahead of print]. doi: 10.3109/19401736.2013.823192
   Google Scholar