| Literature DB >> 30554804 |
Dongxue Ding1, Chunrong Wang1, Zhao Chen1, Huirong Peng1, Kai Li1, Xin Zhou1, Yun Peng1, Puzhi Wang1, Xiaocan Hou1, Tianjiao Li1, Rong Qiu2, Kun Xia3, Jorge Sequeiros4, Tetsuo Ashizawa5, Beisha Tang6, Hong Jiang7.
Abstract
DNA methylation has been reported as an important regulator of genomic structure stability, including large tandem repeats. To test the modulation effect of variants in DNA methylation-related genes on distribution of expanded (CAG)n alleles and age at onset (AO) of patients with Machado-Joseph disease (MJD), we conducted an association analysis on 23 selected SNPs in these genes in 613 patients with MJD and 581 controls. There were significant differences in the distribution of rs12957023 between patients and controls (OR = 1.296, p = 0.007 and OR = 1.206, p = 0.008, for genotype and alleles, respectively). The distribution of (CAG)n size was also different between patients carrying a CC and the other genotypes (TT and TC, p = 0.011 for expanded (CAG)n and p = 0.012 for normal size alleles), indicating that DNA methylation might modulate the (CAG)n instability. We found also that rs13420827 in DNMT3A and rs7354779 in DNMT3L contribute to AO of MJD (p = 0.019 and p = 0.008, respectively). In conclusion, our data provide the first evidence that SNPs in DNA methylation-related genes may contribute to (CAG)n instability and modulate the AO of this disease.Entities:
Keywords: ATXN3; Age at onset; DNA methylation; Epigenetic regulation; MJD; SCA3
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Year: 2018 PMID: 30554804 DOI: 10.1016/j.neurobiolaging.2018.11.002
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673