A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia

创始人效应 单倍型 生物 遗传学 基因分型 单核苷酸多态性 基因 dbSNP公司 智人 1000基因组计划 进化生物学 基因型 地理 考古
作者
Aisen V. Solovyev,Alena Kushniarevich,E. A. Bliznetz,Marita S. Bady-Khoo,M.R. Lalayants,Т Г Маркова,Gabriel Minárik,Ľudevít Kádaši,Ene Metspalu,В.Г. Пшенникова,Fedor M. Teryutin,Э. К. Хуснутдинова,Alexander Poliakov,Mait Metspalu,Olga L. Posukh,Nikolay A. Barashkov,С.А. Федорова
出处
期刊:Human Genetics [Springer Science+Business Media]
卷期号:141 (3-4): 697-707 被引量:5
标识
DOI:10.1007/s00439-021-02405-w
摘要

Mutations in the GJB2 gene are known to be a major cause of autosomal recessive deafness 1A (OMIM 220290). The most common pathogenic variants of the GJB2 gene have a high ethno-geographic specificity in their distribution, being attributed to a founder effect related to the Neolithic migration routes of Homo sapiens. The c.-23 + 1G > A splice site variant is frequently found among deaf patients of both Caucasian and Asian origins. It is currently unknown whether the spread of this mutation across Eurasia is a result of the founder effect or if it could have multiple local centers of origin. To determine the origin of c.-23 + 1G > A, we reconstructed haplotypes by genotyping SNPs on an Illumina OmniExpress 730 K platform of 23 deaf individuals homozygous for this variant from different populations of Eurasia. The analyses revealed the presence of common regions of homozygosity in different individual genomes in the sample. These data support the hypothesis of the common founder effect in the distribution of the c.-23 + 1G > A variant of the GJB2 gene. Based on the published data on the c.-23 + 1G > A prevalence among 16,177 deaf people and the calculation of the TMRCA of the modified f2-haplotypes carrying this variant, we reconstructed the potential migration routes of the carriers of this mutation around the world. This analysis indicates that the c.-23 + 1G > A variant in the GJB2 gene may have originated approximately 6000 years ago in the territory of the Caucasus or the Middle East then spread throughout Europe, South and Central Asia and other regions of the world.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Avalonx应助长命百岁采纳,获得10
刚刚
刚刚
刚刚
刚刚
小马甲应助荔枝采纳,获得10
1秒前
脑洞疼应助倾千奚山采纳,获得10
1秒前
2秒前
代靖宇发布了新的文献求助10
2秒前
3秒前
微笑中道完成签到,获得积分10
4秒前
11111111应助超chao采纳,获得10
4秒前
5秒前
田様应助李文亚采纳,获得10
5秒前
贵月发布了新的文献求助10
6秒前
CodeCraft应助义气的月光采纳,获得10
7秒前
77关注了科研通微信公众号
7秒前
爆米花应助cxf采纳,获得10
7秒前
潇洒迎海发布了新的文献求助10
8秒前
肚肚应助chinwen采纳,获得10
8秒前
8秒前
9秒前
yu发布了新的文献求助10
10秒前
Flllllll完成签到,获得积分10
10秒前
微笑的芝发布了新的文献求助10
10秒前
小二郎应助活力的灰狼采纳,获得10
10秒前
10秒前
解封镝完成签到,获得积分10
10秒前
哇二木耶完成签到,获得积分10
11秒前
Spark发布了新的文献求助10
11秒前
659完成签到,获得积分10
11秒前
11秒前
Alex完成签到,获得积分10
11秒前
aaaaaaa发布了新的文献求助10
12秒前
12秒前
sanvva给apckkk的求助进行了留言
12秒前
13秒前
念念发布了新的文献求助10
13秒前
自然心情发布了新的文献求助10
13秒前
14秒前
hahahaha发布了新的文献求助30
15秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
适配Micro-LED色转换的高兼容性量子点负性光刻胶制备与工艺研究 500
Direct and Iterative Linear System Solvers 500
Vander's Renal Physiology第10版 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7308762
求助须知:如何正确求助?哪些是违规求助? 8926174
关于积分的说明 18916893
捐赠科研通 6971132
什么是DOI,文献DOI怎么找? 3212834
关于科研通互助平台的介绍 2381358
邀请新用户注册赠送积分活动 2190616