Petronis Arturas, Gottesman Irving I, Kan Peixiang, Kennedy James L, Basile Vincenzo S, Paterson Andrew D, Popendikyte Violeta
The Krembil Family Epigenetics Laboratory, Centre for Addiction and Mental Health, 250 College Street, Toronto, Ontario, M5T 1R8 Canada.
Schizophr Bull. 2003;29(1):169-78. doi: 10.1093/oxfordjournals.schbul.a006988.
The goal of this pilot study was to explore the putative molecular mechanisms underlying the phenotypic discordance of monozygotic (MZ) twins. Thus, patterns of epigenetic DNA modification were investigated in the 5'-regulatory region of the dopamine D2 receptor gene (DRD2) in two pairs of monozygotic twins, one concordant and one discordant for schizophrenia. The bisulfite DNA modification-based approach was used to fine-map methylated cytosines in DRD2 in genomic DNA extracted from lymphocytes. Numerous DNA methylation differences were identified in the analyzed region both within and between the pairs of MZ twins. "Epigenetic distances" between MZ twins were calculated and used for the comparison of twin DRD2 methylation profiles. It was detected that the affected twin from the pair discordant for schizophrenia was epigenetically "closer" to the affected concordant twins than to his unaffected MZ co-twin. Although the epigenetic analysis was conducted for only several hundred base pairs of DRD2, the fact that numerous studies identified nonuniform methylation patterns across the clones of bisulfite-modified DNA from the same individual, as well as nonuniform patterns across different individuals, argues for the universality of intra- and interindividual epigenetic variation. Epigenetic studies should provide insight into the molecular causes of differential susceptibility to a disease in genetically identical organisms that may generalize to singletons.
这项初步研究的目的是探索同卵双胞胎表型不一致背后的潜在分子机制。因此,研究了两对同卵双胞胎多巴胺D2受体基因(DRD2)5'调控区的表观遗传DNA修饰模式,其中一对双胞胎患精神分裂症情况一致,另一对不一致。采用基于亚硫酸氢盐DNA修饰的方法对从淋巴细胞中提取的基因组DNA中的DRD2甲基化胞嘧啶进行精细定位。在同卵双胞胎对内部和之间的分析区域中均发现了许多DNA甲基化差异。计算了同卵双胞胎之间的“表观遗传距离”,并用于比较双胞胎DRD2甲基化谱。结果发现,患精神分裂症不一致双胞胎对中的患病双胞胎在表观遗传上与其患病一致的双胞胎“更接近”,而与其未患病的同卵双胞胎“较远”。尽管仅对DRD2的几百个碱基对进行了表观遗传分析,但许多研究发现来自同一个体的亚硫酸氢盐修饰DNA克隆之间存在不均匀的甲基化模式,以及不同个体之间存在不均匀模式,这一事实证明了个体内和个体间表观遗传变异的普遍性。表观遗传研究应能深入了解基因相同的生物体中对疾病易感性差异的分子原因,这些原因可能适用于非双胞胎个体。