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遗传、表观遗传和转录组差异对多发性硬化症双胞胎不一致性的贡献。

Contribution of genetic, epigenetic and transcriptomic differences to twin discordance in multiple sclerosis.

机构信息

Wellcome Trust Centre for Human Genetics and Department of Clinical Neurology, University of Oxford, Oxford, UK.

出版信息

Expert Rev Neurother. 2010 Sep;10(9):1379-81. doi: 10.1586/ern.10.116.

Abstract

Evaluation of: Baranzini SE, Mudge J, van Velkinburgh JC et al. Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis. Nature 464, 1351-1356 (2010). Multiple sclerosis (MS) is a chronic inflammatory disease of the CNS. Genetically identical (monozygotic) twins have a concordance rate for MS of approximately 30%, lending support to the notion that the disease has a complex etiology, developing as a result of genetic and environmental factors and their interactions. However, recent studies have highlighted the fact that monozygotic twins might not actually be genetically identical. In an effort to see if this can explain MS twin discordance, Baranzini and colleagues sequenced the genome from a pair of monozygotic twins discordant for MS, and also examined DNA methylation and gene expression across the genome in this twin pair and an additional two more twin pairs. No consistent differences in DNA sequence, DNA methylation or gene expression were found. Here we put these findings into context and discuss their significance.

摘要

评估

巴兰齐尼 SE、马奇 J、范·韦林克伯格 JC 等人。同卵双胞胎多发性硬化症的基因组、表观基因组和 RNA 序列。自然 464, 1351-1356 (2010)。多发性硬化症(MS)是一种中枢神经系统的慢性炎症性疾病。遗传上相同的(同卵)双胞胎患有 MS 的一致性率约为 30%,这支持了疾病具有复杂病因的观点,是由遗传和环境因素及其相互作用发展而来的。然而,最近的研究强调了一个事实,即同卵双胞胎实际上可能并非在基因上完全相同。为了研究这是否可以解释 MS 双胞胎的不一致性,巴兰齐尼和同事对一对患有 MS 的同卵双胞胎的基因组进行了测序,并在这对双胞胎和另外两对双胞胎中检查了全基因组的 DNA 甲基化和基因表达。未发现 DNA 序列、DNA 甲基化或基因表达存在一致差异。在这里,我们将这些发现置于上下文中,并讨论它们的意义。

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