Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia

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  • Authors: Dzhemileva LU1, Posukh OL2, Barashkov NA3, Fedorova SA3, Teryutin FM3, Akhmetova VL1, Khidiyatova IM1, Khusainova RI1, Lobov SL1, Khusnutdinova EK1
  • Affiliations:
    1. Institute of Biochemistry and Genetics, Ufa Research Center, Russian Academy of Sciences
    2. Institute of Cytology and Genetics, Siberian Branch, Russian Academy of Sciences
    3. Yakut Research Center of Complex Medical Problems, Siberian Branch, Russian Academy of Medical Sciences
  • Issue: Vol 3, No 3 (2011)
  • Pages: 52-63
  • Section: Articles
  • URL: http://actanaturae.ru/2075-8251/article/view/10680
  • DOI: https://doi.org/10.32607/20758251-2011-3-3-52-63
  • Cite item

Abstract


The mutations in the GJB2 (Сх26) gene make the biggest contribution to hereditary hearing loss. The spectrum and prevalence of the GJB2 gene mutations are specific to populations of different ethnic origins. For several GJB2 mutations, their origin from appropriate ancestral founder chromosome was shown, approximate estimations of “age” obtained, and presumable regions of their origin outlined. This work presents the results of the carrier frequencies’ analysis of the major (for European countries) mutation c.35delG (GJB2 gene) among 2,308 healthy individuals from 18 Eurasian populations of different ethnic origins: Bashkirs, Tatars, Chuvashs, Udmurts, Komi-Permyaks, Mordvins, and Russians (the Volga-Ural region of Russia); Byelorussians, Ukrainians (Eastern Europe); Abkhazians, Avars, Cherkessians, and Ingushes (Caucasus); Kazakhs, Uzbeks, Uighurs (Central Asia); and Yakuts, and Altaians (Siberia). The prevalence of the c.35delG mutation in the studied ethnic groups may act as additional evidence for a prospective role of the founder effect in the origin and distribution of this mutation in various populations worldwide. The haplotype analysis of chromosomes with the c.35delG mutation in patients with nonsyndromic sensorineural hearing loss (N=112) and in population samples (N =358) permitted the reconstruction of an ancestral haplotype with this mutation, established the common origin of the majority of the studied mutant chromosomes, and provided the estimated time of the c.35delG mutation carriers expansion (11,800 years) on the territory of the Volga-Ural region.

Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia

L U Dzhemileva

Institute of Biochemistry and Genetics, Ufa Research Center, Russian Academy of Sciences

Email: dzhemilev@anrb.ru

O L Posukh

Institute of Cytology and Genetics, Siberian Branch, Russian Academy of Sciences

N A Barashkov

Yakut Research Center of Complex Medical Problems, Siberian Branch, Russian Academy of Medical Sciences

S A Fedorova

Yakut Research Center of Complex Medical Problems, Siberian Branch, Russian Academy of Medical Sciences

F M Teryutin

Yakut Research Center of Complex Medical Problems, Siberian Branch, Russian Academy of Medical Sciences

V L Akhmetova

Institute of Biochemistry and Genetics, Ufa Research Center, Russian Academy of Sciences

I M Khidiyatova

Institute of Biochemistry and Genetics, Ufa Research Center, Russian Academy of Sciences

R I Khusainova

Institute of Biochemistry and Genetics, Ufa Research Center, Russian Academy of Sciences

S L Lobov

Institute of Biochemistry and Genetics, Ufa Research Center, Russian Academy of Sciences

E K Khusnutdinova

Institute of Biochemistry and Genetics, Ufa Research Center, Russian Academy of Sciences

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Copyright (c) 2011 Dzhemileva L.U., Posukh O.L., Barashkov N.A., Fedorova S.A., Teryutin F.M., Akhmetova V.L., Khidiyatova I.M., Khusainova R.I., Lobov S.L., Khusnutdinova E.K.

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