Mitochondrial ribosome and Ménière’s disease: a pilot study (original) (raw)

References

  1. Silverstein H, Wazen J, Van Ess MJ, Daugherty J, Alameda YA (2010) Intratympanic gentamicin treatment of patients with Meniere’s disease with normal hearing. Otolaryngol Head Neck Surg 142(4):570–575
    Article PubMed Google Scholar
  2. Perez-Delgado L, Fraile-Rodrigo J, Astier-Peña P (2011) Intratympanic gentamicin in Ménière’s disease: our experience. J Laryngol Otol 125:363–369
    Article Google Scholar
  3. Prezant TR, Agapian JV, Bohlman MC, Bu X, Oztas S, Qiu WQ, Arnos KS, Cortopassi GA, Jaber L, Rotter JI et al (1993) Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat Genet 4(3):289–294
    Article PubMed CAS Google Scholar
  4. Zhao H, Li R, Wang Q, Yan Q, Deng JH, Han D, Bai Y, Young WY, Guan MX (2004) Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. Am J Hum Genet 74(1):139–152
    Article PubMed CAS Google Scholar
  5. Vandebona H, Mitchell P, Manwaring N, Griffiths K, Gopinath B, Wang JJ, Sue CM (2009) Prevalence of mitochondrial 1555A → G mutation in adults of European descent. N Engl J Med 360(6):642–644
    Article PubMed CAS Google Scholar
  6. Ruiz-Pesini E, Wallace DC (2006) Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA. Hum Mutat 27(11):1072–1081
    Article PubMed CAS Google Scholar
  7. Vila-Sanjurjo A, Lu Y, Aragonez JL, Starkweather RE, Sasikumar M, O’Connor M (2007) Modulation of 16S rRNA function by ribosomal protein S12. Biochim Biophys Acta 1769(7–8):462–471. doi:10.1016/j.bbaexp.2007.04.004
    PubMed CAS Google Scholar
  8. Cotney J, Wang Z, Shadel GS (2007) Relative abundance of the human mitochondrial transcription system and distinct roles for h-mtTFB1 and h-mtTFB2 in mitochondrial biogenesis and gene expression. Nucleic Acids Res 35(12):4042–4054
    Article PubMed CAS Google Scholar
  9. Equilibrium TCoHa (1995) Committee on Hearing and Equilibrium guidelines for the evaluation of results of treatment of conductive hearing loss. American Academy of Otolaryngology-Head and Neck Surgery Foundation, Inc. Otolaryngol Head Neck Surg 113:186–187
    Article Google Scholar
  10. Gomez-Duran A, Pacheu-Grau D, Lopez-Gallardo E, Diez-Sanchez C, Montoya J, Lopez-Perez MJ, Ruiz-Pesini E (2009) Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups. Hum Mol Genet 19(17):3343–3353
    Article Google Scholar
  11. Ruiz-Pesini E, Lott MT, Procaccio V, Poole JC, Brandon MC, Mishmar D, Yi C, Kreuziger J, Baldi P, Wallace DC (2007) An enhanced MITOMAP with a global mtDNA mutational phylogeny. Nucleic Acids Res 35(Database issue):D823–D828
    Article PubMed CAS Google Scholar
  12. Alonso-Montes C, Castro MG, Reguero JR, Perrot A, Ozcelik C, Geier C, Posch MG, Moris C, Alvarez V, Ruiz-Ortega M, Coto E (2008) Mitochondrial transcription factors TFA, TFB1 and TFB2: a search for DNA variants/haplotypes and the risk of cardiac hypertrophy. Dis Markers 25(3):131–139
    PubMed CAS Google Scholar
  13. Manwaring N, Jones MM, Wang JJ, Rochtchina E, Howard C, Newall P, Mitchell P, Sue CM (2007) Mitochondrial DNA haplogroups and age-related hearing loss. Arch Otolaryngol Head Neck Surg 133(9):929–933
    Article PubMed Google Scholar
  14. Scheunemann AE, Graham WD, Vendeix FA, Agris PF (2010) Binding of aminoglycoside antibiotics to helix 69 of 23S rRNA. Nucleic Acids Res 38(9):3094–3105
    Article PubMed CAS Google Scholar
  15. Shah ZH, Toompuu M, Hakkinen T, Rovio AT, van Ravenswaay C, De Leenheer EM, Smith RJ, Cremers FP, Cremers CW, Jacobs HT (2001) Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness families. Hum Mutat 17(5):433–434. doi:10.1002/humu.1122
    Article PubMed CAS Google Scholar
  16. Pacheu-Grau D, Gomez-Duran A, Lopez-Perez MJ, Montoya J, Ruiz-Pesini E (2010) Mitochondrial pharmacogenomics: barcode for antibiotic therapy. Drug Discov Today 15(1–2):33–39
    Article PubMed CAS Google Scholar
  17. Pacheu-Grau D, Gomez-Duran A, Montoya J, Ruiz-Pesini E (2010) Influence of mtDNA genetic variation on antibiotic therapy. Pharmacogenomics 11(9):1185–1187
    Article PubMed CAS Google Scholar
  18. Chen JM, Williamson PA, Hutchin T, Nedzelski JM, Cortopassi GA (1996) Topical gentamicin-induced hearing loss: a mitochondrial ribosomal RNA study of genetic susceptibility. Am J Otol 17(6):850–852
    PubMed CAS Google Scholar
  19. Walsted A (2001) Unpredictable hearing loss after intratympanic gentamicin treatment for vertigo. A new theory. Acta Otolaryngol 121(1):42–44
    Article PubMed CAS Google Scholar
  20. Guan MX, Yan Q, Li X, Bykhovskaya Y, Gallo-Teran J, Hajek P, Umeda N, Zhao H, Garrido G, Mengesha E, Suzuki T, del Castillo I, Peters JL, Li R, Qian Y, Wang X, Ballana E, Shohat M, Lu J, Estivill X, Watanabe K, Fischel-Ghodsian N (2006) Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations. Am J Hum Genet 79(2):291–302. doi:10.1086/506389
    Article PubMed CAS Google Scholar
  21. Campos Y, Garcia A, Lopez A, Jimenez S, Rubio JC, Del Hoyo P, Bustos F, Martin MA, Cabello A, Ricoy JR, Arenas J (2002) Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy. Muscle Nerve 25(2):185–188. doi:10.1002/mus.10012
    Article PubMed CAS Google Scholar
  22. Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, Chen B, Qian Y, Tang X, Wang J, Zhang X, Guan MX (2008) Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families. Pharmacogenet Genomics 18(12):1059–1070. doi:10.1097/FPC.0b013e3283131661
    Article PubMed CAS Google Scholar

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