Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/136316
Author(s): Li, T
Martins, S
Peng, Y
Wang, P
Hou, X
Chen, Z
Wang, C
Tang, Z
Qiu, R
Chen, C
Hu, Z
Xia, K
Tang, B
Sequeiros, J
Jiang, H
Title: Is the high frequency of machado-joseph disease in China due to new mutational orignis?
Publisher: Frontiers Media
Issue Date: 2019
Abstract: Machado-Joseph disease (MJD, also known as spinocerebellar ataxia 3 or SCA3) is the most common dominant ataxia worldwide, with an overall average prevalence of 1-5/100,000. To this date, two major ancestral lineages have been found throughout the world. In China, the relative frequency of MJD among the SCAs reaches as high as 63%, however, little is known about its mutational origin in this country. We analyzed 50 families with MJD patients in two or more generations to study the hypothesis that new mutational events have occurred in this population. Haplotypes based on 20 SNPs have shown new genetic backgrounds segregating with MJD mutations in our cohort from China. We found the "Joseph-derived" lineage (Joseph lineage with a G variant in rs56268847) to be very common among Chinese MJD patients. Moreover, we estimated the time for the origin of this MJD SNP background based on STR diversity flanking the (CAG)n of ATXN3. It was surprising to find that the Chinese MJD population originated from 8,000 to 17,000 years ago, far earlier than the previous literature reports, which will be an important evidence to explain the origin, spread and founder effects of MJD.
Subject: Founder Effect
Haplotype
Machado-Joseph Disease
Mutational Origins
Sca3
Spinocerebellar Ataxia Type 3
DOI: 10.3389/fgene.2018.00740
URI: https://hdl.handle.net/10216/136316
Source: Frontiers in Genetics, vol.9:740
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
License: https://creativecommons.org/licenses/by/4.0/
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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