Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy.

Da-Yong Wang, Yi-Chen Wang, Dominique Weil, Ya-Li Zhao, Shao-Qi Rao, Liang Zong, Yu-Bin Ji, Qiong Liu, Jian-Qiang Li, Huan-Ming Yang, Yan Shen, Cindy Benedict-Alderfer, Qing-Yin Zheng, Christine Petit, Qiu-Ju Wang
Author Information
  1. Da-Yong Wang: Department of Otolaryngology/Head and Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing 100853, China.

Abstract

BACKGROUND: Mutations in OTOF gene, encoding otoferlin, cause DFNB9 deafness and non-syndromic auditory neuropathy (AN). The aim of this study is to identify OTOF mutations in Chinese patients with non-syndromic auditory neuropathy.
METHODS: 73 unrelated Chinese Han patients with AN, including one case of temperature sensitive non-syndromic auditory neuropathy (TS-NSRAN) and 92 ethnicity-matched controls with normal hearing were screened. Forty-five pairs of PCR primers were designed to amplify all of the exons and their flanking regions of the OTOF gene. The PCR products were sequenced and analyzed for mutation identification.
RESULTS: Five novel possibly pathogenic variants (c.1740delC, c.2975_2978delAG, c.1194T>A, c.1780G>A, c.4819C > T) were identified in the group of 73 AN patients, in which two novel mutant alleles (c.2975_2978delAG + c.4819C > T) were identified in one Chinese TS-NSRAN case. Besides, 10 non-pathogenic variants of the OTOF gene were found in AN patients and controls.
CONCLUSIONS: Screening revealed that mutations in the OTOF gene account for AN in 4 of 73(5.5%) sporadic AN patients, which shows a lower genetic load of that gene in contrast to the previous studies based on other populations. Notably, we found two novel mutant alleles related to temperature sensitive non-syndromic auditory neuropathy. This mutation screening study further confirms that the OTOF gene contributes to ANs and to TS-NSRAN.

References

  1. J Med Genet. 2002 Jul;39(7):502-6 [PMID: 12114484]
  2. Neurobiol Dis. 2002 Jul;10(2):157-64 [PMID: 12127154]
  3. J Med Genet. 2006 Jul;43(7):576-81 [PMID: 16371502]
  4. Hear Res. 2007 Dec;234(1-2):21-8 [PMID: 17967520]
  5. Am J Hum Genet. 2000 Sep;67(3):591-600 [PMID: 10903124]
  6. Clin Genet. 2009 Mar;75(3):237-43 [PMID: 19250381]
  7. Hum Mutat. 2007 Jun;28(6):571-7 [PMID: 17301963]
  8. Nat Genet. 1999 Apr;21(4):363-9 [PMID: 10192385]
  9. Arch Otolaryngol Head Neck Surg. 2002 Sep;128(9):1026-30 [PMID: 12220206]
  10. BMC Dev Biol. 2007 Mar 26;7:21 [PMID: 17386097]
  11. Am J Med Genet A. 2005 Feb 15;133A(1):27-30 [PMID: 15637703]
  12. J Cell Sci. 1997 May;110 ( Pt 9):1073-81 [PMID: 9175703]
  13. Cell. 2006 Oct 20;127(2):277-89 [PMID: 17055430]
  14. Trends Amplif. 2005;9(1):1-43 [PMID: 15920648]
  15. J Med Genet. 2006 Jul;43(7):e33 [PMID: 16816020]
  16. Int J Pediatr Otorhinolaryngol. 2008 Aug;72(8):1135-50 [PMID: 18502518]
  17. J Med Genet. 2003 Jan;40(1):45-50 [PMID: 12525542]
  18. Nature. 2006 Dec 21;444(7122):1013-4 [PMID: 17183302]
  19. N Engl J Med. 2000 Apr 13;342(15):1101-9 [PMID: 10760311]
  20. Brain. 1996 Jun;119 ( Pt 3):741-53 [PMID: 8673487]
  21. Nat Genet. 2006 Jul;38(7):770-8 [PMID: 16804542]
  22. J Basic Clin Physiol Pharmacol. 2000;11(3):215-30 [PMID: 11041385]
  23. Hum Mol Genet. 1996 Jan;5(1):155-8 [PMID: 8789454]
  24. Rev Fac Cien Med Univ Nac Cordoba. 2004;61(1):13-9 [PMID: 15366230]
  25. J Hum Genet. 2009 Jul;54(7):382-5 [PMID: 19461658]
  26. Hum Mutat. 2008 Jun;29(6):823-31 [PMID: 18381613]
  27. Ear Hear. 1998 Jun;19(3):169-79 [PMID: 9657592]

Grants

  1. R01 DC009246/NIDCD NIH HHS

MeSH Term

Animals
Asian People
Base Sequence
Cricetinae
Cricetulus
Deafness
Exons
Family
Hearing Loss
Humans
Membrane Proteins
Mutation
Temperature

Chemicals

Membrane Proteins
OTOF protein, human

Word Cloud

Created with Highcharts 10.0.0OTOFgenecauditoryneuropathyANpatientsnon-syndromicChinesemutations73caseTS-NSRANnovelstudyincludingonetemperaturesensitivecontrolsPCRmutationvariants2975_2978delAG4819C>TidentifiedtwomutantallelesfoundScreeningBACKGROUND:MutationsencodingotoferlincauseDFNB9deafnessaimidentifyMETHODS:unrelatedHan92ethnicity-matchednormalhearingscreenedForty-fivepairsprimersdesignedamplifyexonsflankingregionsproductssequencedanalyzedidentificationRESULTS:Fivepossiblypathogenic1740delC1194T>A1780G>Agroup+Besides10non-pathogenicCONCLUSIONS:revealedaccount455%sporadicshowslowergeneticloadcontrastpreviousstudiesbasedpopulationsNotablyrelatedscreeningconfirmscontributesANsfamilialtemperature-sensitive

Similar Articles

Cited By