[Screening of the mitochondrial 12S rRNA (MTRNR1) gene in probands with sensorineural hearing loss]

Kulak Burun Bogaz Ihtis Derg. 2007;17(2):75-80.
[Article in Turkish]

Abstract

Objectives: We investigated mitochondrial DNA 12S rRNA (MTRNR1) gene mutations as a cause of hearing loss in probands with or without a history of aminoglycoside use.

Patients and methods: The study included 70 patients (40 females, 30 males; age range 3 to 42 years) with nonsyndromic sensorineural hearing loss. Eleven probands had a history of aminoglycoside use before the onset of hearing loss. All cases were first screened and found to be negative for the GJB2 (connexin 26) gene mutations. The m.1555A>G mutation was screened using the PCR-RFLP technique. The entire 12S rRNA gene was later screened with the PCR-TTGE technique followed by direct sequencing.

Results: Of 11 patients with a history of aminoglycoside use, one patient was found to have the m.1555A>G mutation. Two probands with no history of aminoglycoside use exhibited the m.750A>G polymorphism. No pathogenic base substitutions were detected in the remaining patients.

Conclusion: Apart from the common aminoglycoside ototoxicity-related DNA change, m.1555A>G, we could not identify a common mitochondrial 12S rRNA mutation associated with hearing loss in Turkey. Screening of larger series may document rare alterations.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Connexin 26
  • Connexins
  • Female
  • Genes, Mitochondrial / genetics*
  • Genetic Predisposition to Disease*
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Male
  • Mutation
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • RNA, Ribosomal / analysis
  • Turkey
  • White People / genetics

Substances

  • Connexins
  • GJB2 protein, human
  • RNA, Ribosomal
  • RNA, ribosomal, 12S
  • Connexin 26