Cargando…

Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

BACKGROUND: Mutations in GJB2 gene are a major causes of deafness and their spectrum and prevalence are specific for various populations. The well-known mutation c.35delG is more frequent in populations of Caucasian origin. Data on the c.35delG prevalence in Russia are mainly restricted to the Europ...

Descripción completa

Detalles Bibliográficos
Autores principales: Zytsar, Marina V., Barashkov, Nikolay A., Bady-Khoo, Marita S., Shubina-Olejnik, Olga A., Danilenko, Nina G., Bondar, Alexander A., Morozov, Igor V., Solovyev, Aisen V., Danilchenko, Valeriia Yu., Maximov, Vladimir N., Posukh, Olga L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081885/
https://www.ncbi.nlm.nih.gov/pubmed/30086704
http://dx.doi.org/10.1186/s12881-018-0650-5
_version_ 1783345729634304000
author Zytsar, Marina V.
Barashkov, Nikolay A.
Bady-Khoo, Marita S.
Shubina-Olejnik, Olga A.
Danilenko, Nina G.
Bondar, Alexander A.
Morozov, Igor V.
Solovyev, Aisen V.
Danilchenko, Valeriia Yu.
Maximov, Vladimir N.
Posukh, Olga L.
author_facet Zytsar, Marina V.
Barashkov, Nikolay A.
Bady-Khoo, Marita S.
Shubina-Olejnik, Olga A.
Danilenko, Nina G.
Bondar, Alexander A.
Morozov, Igor V.
Solovyev, Aisen V.
Danilchenko, Valeriia Yu.
Maximov, Vladimir N.
Posukh, Olga L.
author_sort Zytsar, Marina V.
collection PubMed
description BACKGROUND: Mutations in GJB2 gene are a major causes of deafness and their spectrum and prevalence are specific for various populations. The well-known mutation c.35delG is more frequent in populations of Caucasian origin. Data on the c.35delG prevalence in Russia are mainly restricted to the European part of this country. We aimed to estimate the carrier frequency of c.35delG in Western Siberia and thereby update current data on the c.35delG prevalence in Russia. According to a generally accepted hypothesis, c.35delG originated from a common ancestor in the Middle East or the Mediterranean ~ 10,000–14,000 years ago and spread throughout Europe with Neolithic migrations. To test the c.35delG common origin hypothesis, we have reconstructed haplotypes bearing c.35delG and evaluated the approximate age of c.35delG in Siberia. METHODS: The carrier frequency of c.35delG was estimated in 122 unrelated hearing individuals living in Western Siberia. For reconstruction of haplotypes bearing c.35delG, polymorphic D13S141, D13S175, D13S1853 flanking the GJB2 gene, and intragenic rs3751385 were genotyped in deaf patients homozygous for c.35delG (n = 24) and in unrelated healthy individuals negative for c.35delG (n = 67) living in Siberia. RESULTS: We present updated carrier rates for c.35delG in Russia complemented by new data on c.35delG carrier frequency in Russians living in Western Siberia (4.1%). Two common D13S141-c.35delG-D13S175-D13S1853 haplotypes, 126-c.35delG-105-202 and 124-c.35delG-105-202, were reconstructed in the c.35delG homozygotes from Siberia. Moreover, identical allelic composition of the two most frequent c.35delG haplotypes restricted by D13S141 and D13S175 was established in geographically remote regions: Siberia and Volga-Ural region (Russia) and Belarus (Eastern Europe). CONCLUSIONS: Distribution of the c.35delG carrier frequency in Russia is characterized by pronounced ethno-geographic specificity with a downward trend from west to east. Comparative analysis of the c.35delG haplotypes supports a common origin of c.35delG in some regions of Russia (Volga-Ural region and Siberia) and in Eastern Europe (Belarus). A rough estimation of the c.35delG age in Siberia (about 4800 to 8100 years ago) probably reflects the early formation stages of the modern European population (including the European part of the contemporary territory of Russia) since the settlement of Siberia by Russians started only at the end of sixteenth century. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-018-0650-5) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6081885
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-60818852018-08-10 Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia Zytsar, Marina V. Barashkov, Nikolay A. Bady-Khoo, Marita S. Shubina-Olejnik, Olga A. Danilenko, Nina G. Bondar, Alexander A. Morozov, Igor V. Solovyev, Aisen V. Danilchenko, Valeriia Yu. Maximov, Vladimir N. Posukh, Olga L. BMC Med Genet Research Article BACKGROUND: Mutations in GJB2 gene are a major causes of deafness and their spectrum and prevalence are specific for various populations. The well-known mutation c.35delG is more frequent in populations of Caucasian origin. Data on the c.35delG prevalence in Russia are mainly restricted to the European part of this country. We aimed to estimate the carrier frequency of c.35delG in Western Siberia and thereby update current data on the c.35delG prevalence in Russia. According to a generally accepted hypothesis, c.35delG originated from a common ancestor in the Middle East or the Mediterranean ~ 10,000–14,000 years ago and spread throughout Europe with Neolithic migrations. To test the c.35delG common origin hypothesis, we have reconstructed haplotypes bearing c.35delG and evaluated the approximate age of c.35delG in Siberia. METHODS: The carrier frequency of c.35delG was estimated in 122 unrelated hearing individuals living in Western Siberia. For reconstruction of haplotypes bearing c.35delG, polymorphic D13S141, D13S175, D13S1853 flanking the GJB2 gene, and intragenic rs3751385 were genotyped in deaf patients homozygous for c.35delG (n = 24) and in unrelated healthy individuals negative for c.35delG (n = 67) living in Siberia. RESULTS: We present updated carrier rates for c.35delG in Russia complemented by new data on c.35delG carrier frequency in Russians living in Western Siberia (4.1%). Two common D13S141-c.35delG-D13S175-D13S1853 haplotypes, 126-c.35delG-105-202 and 124-c.35delG-105-202, were reconstructed in the c.35delG homozygotes from Siberia. Moreover, identical allelic composition of the two most frequent c.35delG haplotypes restricted by D13S141 and D13S175 was established in geographically remote regions: Siberia and Volga-Ural region (Russia) and Belarus (Eastern Europe). CONCLUSIONS: Distribution of the c.35delG carrier frequency in Russia is characterized by pronounced ethno-geographic specificity with a downward trend from west to east. Comparative analysis of the c.35delG haplotypes supports a common origin of c.35delG in some regions of Russia (Volga-Ural region and Siberia) and in Eastern Europe (Belarus). A rough estimation of the c.35delG age in Siberia (about 4800 to 8100 years ago) probably reflects the early formation stages of the modern European population (including the European part of the contemporary territory of Russia) since the settlement of Siberia by Russians started only at the end of sixteenth century. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-018-0650-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-07 /pmc/articles/PMC6081885/ /pubmed/30086704 http://dx.doi.org/10.1186/s12881-018-0650-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zytsar, Marina V.
Barashkov, Nikolay A.
Bady-Khoo, Marita S.
Shubina-Olejnik, Olga A.
Danilenko, Nina G.
Bondar, Alexander A.
Morozov, Igor V.
Solovyev, Aisen V.
Danilchenko, Valeriia Yu.
Maximov, Vladimir N.
Posukh, Olga L.
Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia
title Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia
title_full Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia
title_fullStr Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia
title_full_unstemmed Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia
title_short Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia
title_sort updated carrier rates for c.35delg (gjb2) associated with hearing loss in russia and common c.35delg haplotypes in siberia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081885/
https://www.ncbi.nlm.nih.gov/pubmed/30086704
http://dx.doi.org/10.1186/s12881-018-0650-5
work_keys_str_mv AT zytsarmarinav updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT barashkovnikolaya updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT badykhoomaritas updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT shubinaolejnikolgaa updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT danilenkoninag updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT bondaralexandera updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT morozovigorv updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT solovyevaisenv updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT danilchenkovaleriiayu updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT maximovvladimirn updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia
AT posukholgal updatedcarrierratesforc35delggjb2associatedwithhearinglossinrussiaandcommonc35delghaplotypesinsiberia