Corrigendum to "The effect of the mtDNA4834 deletion on hearing" [Biochem. Biophys. Res. Commun. 344 (2006) 425-430] (DOI:10.1016/j.bbrc.2006.03.060);The effect of the mtDNA4834 deletion on hearing

Biochemical and Biophysical Research Communications

Volumn 344, Issue 1, 2006, Pages 425-430

  Kong, Wei Jia ^a   Hu, Yu Juan ^a   Wang, Qiong ^a,b   Wang, Ying ^a   Han, Yue Chen ^a,c   Cheng, Hua Mao ^a   Kong, Wen ^a   Guan, Min Xin ^d,e  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b AMERICAN HEART ASSOCIATION   (United States)

^c SHANDONG PROVINCIAL HOSPITAL AFFILIATED TO SHANDONG UNIVERSITY   (China)

^d CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^e UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

Aminoglycoside antibiotic; Common deletion; d Galactose; Mitochondrial DNA; Presbyacusis; Stress

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT; GALACTOSE; MALONALDEHYDE; MITOCHONDRIAL DNA; SUPEROXIDE DISMUTASE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDITORY THRESHOLD; CONTROLLED STUDY; DNA SEQUENCE; GENE DELETION; GENETIC PREDISPOSITION; HEARING; HEARING LOSS; INJECTION; INNER EAR; NONHUMAN; PRESBYACUSIS; PRIORITY JOURNAL; RAT; SEQUENCE ANALYSIS;

ANIMALIA;

EID: 33646040687     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.06.123     Document Type: Erratum

References (28)

1. Fischel-Ghodsian N., Prezant T.R., Fournier P., Stewart I.A., and Maw M. Mitochondrial mutation associated with nonsyndromic deafness. Am. J. Otolaryngol. 16 (1995) 403-408
2. Prezant T.R., Agapian J.V., Bohlman M.C., Bu X., Öztas S., Qiu W.Q., Arnos K.S., Cortopassi G.A., Jaber L., Rotter J.I., Shohat M., and Fischel-Ghodsian N. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat. Genet. 427 (1993) 289-294
3. Ballinger S.W., Shoffner J.M., Hedaya E.V., Trounce I., Polak M.A., Koontz D.A., and Wallace D.C. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial deletion. Nat. Genet. 1 (1992) 11-15
4. Fischel-Ghodsian N., Bykhovskaya Y., Taylor K., Kahen T., Cantor R., Ehrenman K., Smith R., and Keithley E. Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations. Hear. Res. 110 (1997) 147-154
5. Seidman M.D., Bai U., Khan M.J., and Quirk W.S. Mitochondrial DNA deletions associated with aging and presbyacusis. Arch. Otolaryngol. Head Neck Surg. 123 (1997) 1039-1045
6. Nagley P., Mackay I.R., Baumer A., Maxwell R.J., Vaillant F., Wang Z.X., Zhang C., and Linnane A.W. Mitochondrial DNA mutation associated with aging and degenerative disease. Ann. N. Y. Acad. Sci. 673 (1992) 92-102
7. Rotig A., Bourgeron T., Chretien D., Rustin P., and Munnich A. Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome. Hum. Mol. Genet. 4 (1995) 1327-1330
8. Moraes C.T., DiMauro S., Zeviani M., Lombes A., Shanske S., Miranda A.F., Nakase H., Bonilla E., Werneck L.C., Servidei S., et al. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome. N. Engl. J. Med. 320 (1989) 1293-1299
9. Wallace D.C. Mitochondrial genetics: a paradigm for aging and degenerative diseases?. Science 256 (1992) 628-632
10. Bai U., Seidman M.D., Hinojosa R., and Quirk W.S. Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study. Am. J. Otol. 18 (1997) 449-453
11. Ueda N., Oshima T., Ikeda K., Abe K., Aoki M., and Takasaka T. Mitochondrial DNA deletion is a predisposing cause for sensorineural hearing loss. Laryngoscope 108 (1998) 580-584
12. Kong W., Wang Q., Zheng X., and Cheng H. Mitochondrial DNA mutations and non-syndromic sensorineural hearing loss. Zhonghua Er Bi Yan Hou Ke Za Zhi 37 (2002) 338-342
13. Thayer R.E., Wittock R., Parr R., Zullo S., and Birch-Machin M.A. A maternal line study investigating the 4977-bp mitochondrial DNA deletion. Exp. Gerontol. 38 (2003) 567-571
14. Edris W., Burgett B., Stine O.C., and Filburn C.R. Detection and quantitation by competitive PCR of an age-associated increase in a 4.8 kb deletion in rat mitochondrial DNA. Mutat. Res. 316 (1994) 69-78
15. Gadaleta M.N., Rainaldi G., Lezza A.M., Milella F., and Fracasso F. Cantatore P Mitochondrial DNA copy number and mitochondrial DNA deletion in adult and senescent rats. Mutat. Res. 275 (1992) 181-193
16. Shi C.H., Jue H.L., and Wu Y. ReY, Establishment of the mimetic aging effect in mice caused by d-galactose. Biogerontology 4 (2003) 15-18
17. Song X., Bao M., Li D., and Li Y.M. Advanced glycation in d-galactose induced mouse aging model. Mech. Ageing 108 (1999) 239-251
18. Wei H., Li L., Song Q., Ai H., Chu J., and Li W. Behavioural study of the d-galactose induced aging model in C57BL/6J mice. Behav. Brain Res. 157 (2005) 245-251
19. Nedic O., Rodic-Strugar J., Solak Z., and Filipovic D. Noise as a stress factor for the onset of hearing disorders in workers using drilling equipment. Med. Pregl. 54 (2001) 267-272
20. Lautermann J., Dehne N., Schacht J., and Jahnke K. Aminoglycoside- and cisplatin-ototoxicity: from basic science to clinics. Laryngorhinootologie 83 (2004) 317-323
21. Sha S.H., and Schacht J. Formation of reactive oxygen species following bioactivation of gentamicin. Free Radic. Biol. Med. 26 (1999) 341-347
22. Prithivirajsingh S., Story M.D., Bergh S.A., Geara F.B., Ang K.K., Ismail S.M., Stevens C.W., Buchholz T.A., and Brock W.A. Accumulation of the common mitochondrial DNA deletion induced by ionizing radiation. FEBS Lett. 571 (2004) 227-232
23. Zeng Z., Zhang Z., Yu H., Corbley M.J., Tang Z., and Tong T. Mitochondrial DNA deletions are associated with ischemia and aging in Balb/c mouse brain. J. Cell. Biochem. 73 (1999) 545-553
24. Wang Z. Physiologic and biochemical changes of mimetic aging induced by d-galactose in rats. Lab. Anim. Sci. Adm. 16 (1999) 23-25
25. Bai U., and Seidman M.D. A specific mitochondrial DNA deletion (mtDNA4977) is identified in a pedigree of a family with hearing loss. Hear. Res. 154 (2001) 73-80
26. Guan M.X., Fischel-Ghodsian N., and Attardi G. Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation. Hum. Mol. Genet. 5 (1996) 963-971
27. Estivill X., Govea N., Barcelo E., Badenas C., Romero E., Moral L., Scozzri R., D'Urbano L., Zeviani M., and Torroni A. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides. Am. J. Hum. Genet. 62 (1998) 27-35
28. Torroni A., Petrozzi M., D'Urbano L., Sellitto D., Zeviani M., Carrara F., Carducci C., Leuzzi V., Carelli V., Barboni P., De Negri A., and Scozzari R. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am. J. Hum. Genet. 60 (1997) 1107-1121