Publication Cover
Mitochondrial DNA Part A
DNA Mapping, Sequencing, and Analysis
Volume 27, 2016 - Issue 4
129
Views
1
CrossRef citations to date
0
Altmetric
Short Communication

Mitochondrial tRNA mutations in patients with myelodysplastic syndromes

, , &
Pages 2315-2317 | Received 12 Jan 2015, Accepted 15 Feb 2015, Published online: 26 Mar 2015

References

  • Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, et al. (1981). Sequence and organization of the human mitochondrial genome. Nature 290:457–65
  • Berger G, Hunault-Berger M, Rachieru P, Fontenay-Roupie M, Baranger L, Ifrah N, Zandecki M. (2001). Increased apoptosis in mononucleated cells but not in CD34+ cells in blastic forms of myelodysplastic syndromes. Hematology 2:87–96
  • Garcia-Manero G. (2011). Myelodysplastic syndromes update on diagnosis, risk-stratification, and management. Am J Hematol 86:490–8
  • Gattermann N. (2000). From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes. Leuk Res 24:141–51
  • Gotz A, Isohanni P, Liljestrom B, Rummukainen J, Nikolajev K, Herrgard E, Marjavaara S, Suomalainen A. (2012). Fatal neonatal lactic acidosis caused by a novel de novo mitochondrial G7453A tRNA-Serine (UCN) mutation. Pediatr Res 72:90–4
  • Gupta M, Madkaikar M, Rao VB, Mishra A, Govindaraj P, Thangaraj K, Ghosh K. (2013). Mitochondrial DNA variations in myelodysplastic syndrome. Ann Hematol 92:871–6
  • 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
  • Liu VW, Shi HH, Cheung AN, Chiu PM, Leung TW, Nagley P, Wong LC, Ngan HY. (2001). High incidence of somatic mitochondrial DNA mutations in human ovarian carcinomas. Cancer Res 61:5998–6001
  • Lu J, Qian Y, Li Z, Yang A, Zhu Y, Li R, Yang L, et al. (2010). Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A > G mutation. Mitochondrion 10:69–81
  • Matthes TW, Meyer G, Samii K, Beris P. (2000). Increased apoptosis in acquired sideroblastic anaemia. Br J Haematol 111:843–52
  • Mimaki M, Hatakeyama H, Ichiyama T, Isumi H, Furukawa S, Akasaka M, Kamei A, et al. (2009). Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders. Mitochondrion 9:115–22
  • Pei H, Peng Q, Lan C, Chi Liu B. (2014). Variations in mitochondrial tRNAThr gene may not be associated with coronary heart disease. Mitochondrial DNA. [Epub ahead of print]
  • Shtil/bans A, El-Schahawi M, Malkin E, Shanske S, Musumeci O, DiMauro S. (1999). A novel mutation in the mitochondrial DNA transfer ribonucleic acid Asp gene in a child with myoclonic epilepsy and psychomotor regression. J Child Neurol 9:610–13
  • Silvestri G, Mongini T, Odoardi F, Modoni A, deRosa G, Doriguzzi C, Palmucci L, et al. (2000). A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency. Neurology 54:1693–6
  • van de Loosdrecht AA, Brada SJ, Blom NR, Hendriks DW, Smit JW, van den Berg E, de Wolf JT, Vellenga E. (2001). Mitochondrial disruption and limited apoptosis of erythroblasts are associated with high risk myelodysplasia. An ultrastructural analysis. Leuk Res 25:385–93
  • Wei L, Gao W, Ma Y, Cao Q, Zhang X. (2014). Is mitochondrial tRNACys G5821A a deleterious mutation? Mitochondrial DNA. [Epub ahead of print]
  • Wortmann SB, Champion MP, van den Heuvel L, Barth H, Trutnau B, Craig K, Lammens M, et al. (2012). Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction? Eur J Med Genet 55:552–6
  • Wulfert M, Küpper AC, Tapprich C, Bottomley SS, Bowen D, Germing U, Haas R, Gattermann N. (2008). Analysis of mitochondrial DNA in 104 patients with myelodysplastic syndromes. Exp Hematol 36:577–86
  • Yarham JW, Elson JL, Blakely EL, McFarland R, Taylor RW. (2010). Mitochondrial tRNA mutations and disease. Wiley Interdiscip Rev RNA 1:304–24
  • Zhu HY, Wang SW, Liu L, Chen R, Wang L, Gong XL, Zhang ML. (2009). Genetic variants in mitochondrial tRNA genes are associated with essential hypertension in a Chinese Han population. Clin Chim Acta 410:64–9
  • Zhuo G, Ding Y, Feng G, Yu L, Jiang Y. (2012). Analysis of mitochondrial DNA sequence variants in patients with polycystic ovary syndrome. Arch Gynecol Obstet 286:653–9

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.