Literature DB >> 25376778

Mutations in the mitochondrial 12S rRNA gene in elderly Chinese people.

Yuhua Zhu1, Jiandong Zhao, Bo Feng, Yu Su, Dongyang Kang, Huijun Yuan, Suoqiang Zhai, Pu Dai.   

Abstract

CONCLUSION: Our data indicate that the mitochondrial 12S rRNA gene, and particularly the A827G mutation, may be associated with susceptibility to age-related hearing loss.
OBJECTIVE: Hearing loss associated with aging is common among elderly persons. In all genetic backgrounds, mitochondrial DNA (mtDNA) mutations may be one of the most important factors contributing to aging and age-related hearing loss. The mitochondrial 12S rRNA is a hot spot for deafness-associated mutations in Chinese populations. The purpose of the present study was to elucidate the relationship of 12S rRNA gene polymorphisms and age-related hearing loss.
METHODS: The 12S rRNA gene polymorphisms were detected by direct sequencing. Statistical analyses were performed to assess the associations between age-related hearing loss and 12S rRNA gene variants.
RESULTS: We report here a systematic mutational screening of the mitochondrial 12S rRNA gene in 662 elderly subjects from the general population with various hearing threshold levels (211 controls and 451 age-related hearing loss subjects). Mutational screening of the mitochondrial 12S rRNA gene identified 55 nucleotide changes, including 4 mutations localized at highly conserved sites and 51 known variants. Of the known deafness-associated mutations in the mitochondrial 12S rRNA gene, the incidence of the A1555G mutation was 0.15%, A827G was 4.38%, T1095C was 0.45%, and T1005C was 3.78%. The incidence of the other known variants was 0.15-99.85%. We found statistically significant differences in the proportions of subjects with the A827G mutation among the various age-related hearing loss groups and normal controls.

Entities:  

Keywords:  Hearing loss; age-related hearing loss; hereditary susceptibility; mitochondrial DNA; presbycusis

Mesh:

Substances:

Year:  2014        PMID: 25376778     DOI: 10.3109/00016489.2014.949849

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  6 in total

1.  Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation.

Authors:  Ping Gu; Guojian Wang; Xue Gao; Dongyang Kang; Pu Dai; Shasha Huang
Journal:  BMC Med Genomics       Date:  2022-05-25       Impact factor: 3.622

Review 2.  PharmGKB summary: very important pharmacogene information for MT-RNR1.

Authors:  Julia M Barbarino; Tracy L McGregor; Russ B Altman; Teri E Klein
Journal:  Pharmacogenet Genomics       Date:  2016-12       Impact factor: 2.089

3.  Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry.

Authors:  Rogério Marins Alves; Sueli Matilde da Silva Costa; Paulo Mauricio do Amôr Divino Miranda; Priscila Zonzini Ramos; Thiago Gibbin Marconi; Gisele Santos Oliveira; Arthur Menino Castilho; Edi Lúcia Sartorato
Journal:  BMC Med Genet       Date:  2016-05-26       Impact factor: 2.103

4.  The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis.

Authors:  Masoumeh Falah; Massoud Houshmand; Mohammad Najafi; Maryam Balali; Saeid Mahmoudian; Alimohamad Asghari; Hessamaldin Emamdjomeh; Mohammad Farhadi
Journal:  Ther Clin Risk Manag       Date:  2016-10-19       Impact factor: 2.423

5.  Association of genetic variations in the mitochondrial DNA control region with presbycusis.

Authors:  Masoumeh Falah; Mohammad Farhadi; Seyed Kamran Kamrava; Saeid Mahmoudian; Ahmad Daneshi; Maryam Balali; Alimohamad Asghari; Massoud Houshmand
Journal:  Clin Interv Aging       Date:  2017-03-03       Impact factor: 4.458

6.  A Mitochondrial DNA Variant Elevates the Risk of Gallstone Disease by Altering Mitochondrial Function.

Authors:  Dayan Sun; Zhenmin Niu; Hong-Xiang Zheng; Fei Wu; Liuyiqi Jiang; Tian-Quan Han; Yang Wei; Jiucun Wang; Li Jin
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2020-12-04
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.