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Volumn 377, Issue 2, 2008, Pages 379-383

Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy

Author keywords

12S rRNA; Aminoglycoside toxicity; Bilateral vestibulopathy; Hearing loss; mtDNA; Mutation

Indexed keywords

AMINOGLYCOSIDE; MITOCHONDRIAL RNA; RNA 12S;

EID: 55549121904     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2008.09.134     Document Type: Article
Times cited : (22)

References (33)
  • 4
    • 37849038231 scopus 로고    scopus 로고
    • Recent advances in the genetics of recurrent vertigo and vestibulopathy
    • Jen J.C. Recent advances in the genetics of recurrent vertigo and vestibulopathy. Curr. Opin. Neurol. 21 (2008) 3-7
    • (2008) Curr. Opin. Neurol. , vol.21 , pp. 3-7
    • Jen, J.C.1
  • 7
    • 33644547013 scopus 로고    scopus 로고
    • Molecular understanding of aminoglycoside action and resistance
    • Jana S., and Deb J.K. Molecular understanding of aminoglycoside action and resistance. Appl. Microbiol. Biotechnol. (2006) 1-11
    • (2006) Appl. Microbiol. Biotechnol. , pp. 1-11
    • Jana, S.1    Deb, J.K.2
  • 8
    • 0030827973 scopus 로고    scopus 로고
    • Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness
    • Hamasaki K., and Rando R.R. Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness. Biochemistry 36 (1997) 12323-12380
    • (1997) Biochemistry , vol.36 , pp. 12323-12380
    • Hamasaki, K.1    Rando, R.R.2
  • 9
    • 46249111398 scopus 로고    scopus 로고
    • Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature
    • Berrettini S., Forli F., Passetti S., Rocchi A., Pollina L., Cecchetti D., Mancuso M., and Siciliano G. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature. Biosci. Rep. 28 (2008) 49-59
    • (2008) Biosci. Rep. , vol.28 , pp. 49-59
    • Berrettini, S.1    Forli, F.2    Passetti, S.3    Rocchi, A.4    Pollina, L.5    Cecchetti, D.6    Mancuso, M.7    Siciliano, G.8
  • 11
    • 33847000885 scopus 로고    scopus 로고
    • Histopathology of the vestibular end organs after intratympanic gentamicin failure for Meniere's disease
    • Ishiyama G., Lopez I., Baloh R.W., and Ishiyama A. Histopathology of the vestibular end organs after intratympanic gentamicin failure for Meniere's disease. Acta Otolaryngol. 127 (2007) 34-40
    • (2007) Acta Otolaryngol. , vol.127 , pp. 34-40
    • Ishiyama, G.1    Lopez, I.2    Baloh, R.W.3    Ishiyama, A.4
  • 12
    • 35248821352 scopus 로고    scopus 로고
    • Vestibular system in infants after systemic aminoglycoside therapy
    • Zagólski O. Vestibular system in infants after systemic aminoglycoside therapy. Int. J. Pediatr. Otorhinolaryngol. 71 (2007) 1797-1802
    • (2007) Int. J. Pediatr. Otorhinolaryngol. , vol.71 , pp. 1797-1802
    • Zagólski, O.1
  • 13
    • 0030716844 scopus 로고    scopus 로고
    • Clinical-pathologic correlation in a patient with selective loss of hair cells in the vestibular endorgans
    • Baloh R.W., Lopez I., Beykirch K., Ishiyama A., and Honrubia V. Clinical-pathologic correlation in a patient with selective loss of hair cells in the vestibular endorgans. Neurology 49 (1997) 1377-1820
    • (1997) Neurology , vol.49 , pp. 1377-1820
    • Baloh, R.W.1    Lopez, I.2    Beykirch, K.3    Ishiyama, A.4    Honrubia, V.5
  • 15
    • 0029832209 scopus 로고    scopus 로고
    • Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides
    • Braverman I., Jaber L., Levi H., Adelman C., Arons K.S., Fischel-Ghodsian N., Shohat M., and Elidan J. Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides. Arch. Otolaryngol. Head Neck Surg. 122 (1996) 1001-1004
    • (1996) Arch. Otolaryngol. Head Neck Surg. , vol.122 , pp. 1001-1004
    • Braverman, I.1    Jaber, L.2    Levi, H.3    Adelman, C.4    Arons, K.S.5    Fischel-Ghodsian, N.6    Shohat, M.7    Elidan, J.8
  • 16
    • 0035134021 scopus 로고    scopus 로고
    • Different clinical characteristics of aminoglycoside-induced profound deafness with and without the 1555 A>G mitochondrial mutation
    • Tono T., Kiyomizu K., Matsuda K., Komune S., Usami S., Abe S., and Shinkawa H. Different clinical characteristics of aminoglycoside-induced profound deafness with and without the 1555 A>G mitochondrial mutation. ORL J. Otorhinolaryngol. Relat. Spec. 63 (2001) 25-30
    • (2001) ORL J. Otorhinolaryngol. Relat. Spec. , vol.63 , pp. 25-30
    • Tono, T.1    Kiyomizu, K.2    Matsuda, K.3    Komune, S.4    Usami, S.5    Abe, S.6    Shinkawa, H.7
  • 17
    • 0842277862 scopus 로고    scopus 로고
    • Audiovestibular findings in patients with mitochondrial A1555G mutation
    • Noguchi Y., Yashima T., Ito T., Sumi T., Tsuzuku T., and Kitamura K. Audiovestibular findings in patients with mitochondrial A1555G mutation. Laryngoscope 114 (2004) 344-348
    • (2004) Laryngoscope , vol.114 , pp. 344-348
    • Noguchi, Y.1    Yashima, T.2    Ito, T.3    Sumi, T.4    Tsuzuku, T.5    Kitamura, K.6
  • 18
    • 33644875533 scopus 로고    scopus 로고
    • MtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences
    • Ingman M., and Gyllensten U. MtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences. Nucleic Acids Res. 34 (2006) D749-D751
    • (2006) Nucleic Acids Res. , vol.34
    • Ingman, M.1    Gyllensten, U.2
  • 21
    • 7444244924 scopus 로고    scopus 로고
    • Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enough
    • McFarland R., Elson J.L., Taylor R.W., Howell N., and Turnbull D.M. Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enough. Trends Genet. 20 (2004) 591-596
    • (2004) Trends Genet. , vol.20 , pp. 591-596
    • McFarland, R.1    Elson, J.L.2    Taylor, R.W.3    Howell, N.4    Turnbull, D.M.5
  • 23
    • 0030601096 scopus 로고    scopus 로고
    • Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells
    • Inoue K., Takai D., Soejima A., Isobe K., Yamasoba T., Oka Y., Goto Y., and Hayashi J. Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells. Biochem. Biophys. Res. Commun. 223 (1996) 496-501
    • (1996) Biochem. Biophys. Res. Commun. , vol.223 , pp. 496-501
    • Inoue, K.1    Takai, D.2    Soejima, A.3    Isobe, K.4    Yamasoba, T.5    Oka, Y.6    Goto, Y.7    Hayashi, J.8
  • 24
    • 0347003512 scopus 로고    scopus 로고
    • 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
    • Zhao H., Li R., Wang Q., Yan Q., Deng J.H., Han D., Bai Y., Young W.Y., and Guan M.X. 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 (2004) 139-152
    • (2004) Am. J. Hum. Genet. , vol.74 , pp. 139-152
    • Zhao, H.1    Li, R.2    Wang, Q.3    Yan, Q.4    Deng, J.H.5    Han, D.6    Bai, Y.7    Young, W.Y.8    Guan, M.X.9
  • 25
    • 19944430235 scopus 로고    scopus 로고
    • Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation
    • Wang Q., Li R., Zhao H., Peters J.L., Liu Q., Yang L., Han D., Greinwald J.H.J., Young W.Y., and Guan M.X. Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation. Am. J. Med. Genet. A 133A (2005) 27-30
    • (2005) Am. J. Med. Genet. A , vol.133 A , pp. 27-30
    • Wang, Q.1    Li, R.2    Zhao, H.3    Peters, J.L.4    Liu, Q.5    Yang, L.6    Han, D.7    Greinwald, J.H.J.8    Young, W.Y.9    Guan, M.X.10
  • 26
    • 33646185290 scopus 로고    scopus 로고
    • A reappraisal of complete mtDNA variation in East Asian families with hearing impairment
    • Yao Y.G., Salas A., Bravi C.M., and Bandelt H.J. A reappraisal of complete mtDNA variation in East Asian families with hearing impairment. Hum. Genet. 119 (2006) 505-515
    • (2006) Hum. Genet. , vol.119 , pp. 505-515
    • Yao, Y.G.1    Salas, A.2    Bravi, C.M.3    Bandelt, H.J.4
  • 27
    • 0029003553 scopus 로고
    • Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness
    • Bacino C., Prezant T.R., Bu X., Fournier P., and Fischel-Ghodsian N. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness. Pharmacogenetics 5 (1995) 165-172
    • (1995) Pharmacogenetics , vol.5 , pp. 165-172
    • Bacino, C.1    Prezant, T.R.2    Bu, X.3    Fournier, P.4    Fischel-Ghodsian, N.5
  • 29
    • 0344167734 scopus 로고    scopus 로고
    • Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss
    • Li R., Xing G., Yan M., Cao X., Liu X.Z., Bu X., and Guan M.X. Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss. Am. J. Med. Genet. A 124 (2004) 113-117
    • (2004) Am. J. Med. Genet. A , vol.124 , pp. 113-117
    • Li, R.1    Xing, G.2    Yan, M.3    Cao, X.4    Liu, X.Z.5    Bu, X.6    Guan, M.X.7
  • 30
    • 4043089861 scopus 로고    scopus 로고
    • Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss
    • Li R., Greinwald J.H.J., Yang L., Choo D.I., Wenstrup R.J., and Guan M.X. Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss. J. Med. Genet. 41 (2004) 615-620
    • (2004) J. Med. Genet. , vol.41 , pp. 615-620
    • Li, R.1    Greinwald, J.H.J.2    Yang, L.3    Choo, D.I.4    Wenstrup, R.J.5    Guan, M.X.6
  • 31
    • 20344407298 scopus 로고    scopus 로고
    • Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss
    • Li Z., Li R., Chen J., Liao Z., Zhu Y., Qian Y., Xiong S., Heman-Ackah S., Wu J., Choo D.I., and Guan M.X. Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss. Hum. Genet. 117 (2005) 9-15
    • (2005) Hum. Genet. , vol.117 , pp. 9-15
    • Li, Z.1    Li, R.2    Chen, J.3    Liao, Z.4    Zhu, Y.5    Qian, Y.6    Xiong, S.7    Heman-Ackah, S.8    Wu, J.9    Choo, D.I.10    Guan, M.X.11
  • 32
    • 8844236333 scopus 로고    scopus 로고
    • Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation
    • Zhao L., Young W.Y., Li R., Wang Q., Qian Y., and Guan M.X. Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation. Biochem. Biophys. Res. Commun. 325 (2004) 1503-1508
    • (2004) Biochem. Biophys. Res. Commun. , vol.325 , pp. 1503-1508
    • Zhao, L.1    Young, W.Y.2    Li, R.3    Wang, Q.4    Qian, Y.5    Guan, M.X.6


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