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由脆性X基因FMR1的DNA甲基化模式所阐明的表观遗传变异。

Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1.

作者信息

Stöger R, Kajimura T M, Brown W T, Laird C D

机构信息

Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

出版信息

Hum Mol Genet. 1997 Oct;6(11):1791-801. doi: 10.1093/hmg/6.11.1791.

Abstract

Genomic methylation patterns of mammals can vary among individuals and are subject to dynamic changes during development. In order to gain a better understanding of this variation, we have analyzed patterns of cytosine methylation within a 200 bp region at the CpG island of the human FMR1 gene from leukocyte DNA. FMR1 is normally methylated during inactivation of the X chromosome in females and it is also methylated and inactivated upon expansion of CGG repeats in fragile-X syndrome. Patterns of methylation (epigenotypes) were determined by the sequencing of bisulfite-treated alleles from normal males and females and alleles from a family of five brothers who are methylation mosaics and are affected to various degrees by the fragile-X syndrome. Our data indicate that: (i) methylation of individual CpG cytosines is strikingly variable in hypermethylated epigenotypes obtained from a single individual, suggesting that maintenance of cytosine methylation is a dynamic process; (ii) methylation of non-CpG cytosines in the region studied may occur but is rare; (iii) mosaicism of methylation in the analyzed fragile-X males is remarkably similar to that found for the active X and inactive X alleles in normal females, suggesting that the methylation mosaicism of some fragile-X males reflects similar on and off states of FMR1 expression that exist in normal females; (iv) hypermethylation is slightly more pronounced on fragile-X alleles than on normal inactive X alleles of females; (v) the general dichotomy of hypo- and hypermethylated alleles persisted over the 5 year period that separated samplings of the fragile-X males; (vi) methylation variability was most pronounced at a consensus binding sequence for the alpha-PAL transcription factor, a sequence that may play a role in regulating expression of FMR1.

摘要

哺乳动物的基因组甲基化模式在个体间存在差异,并且在发育过程中会发生动态变化。为了更好地理解这种变异,我们分析了来自白细胞DNA的人类FMR1基因CpG岛中一个200bp区域内的胞嘧啶甲基化模式。FMR1在女性X染色体失活期间通常会发生甲基化,并且在脆性X综合征中,随着CGG重复序列的扩增,它也会被甲基化并失活。通过对正常男性和女性经亚硫酸氢盐处理的等位基因以及来自一个五兄弟家庭的等位基因进行测序,确定了甲基化模式(表观基因型),这五兄弟都是甲基化镶嵌体,并且不同程度地受到脆性X综合征的影响。我们的数据表明:(i)在从单个个体获得的高甲基化表观基因型中,单个CpG胞嘧啶的甲基化具有显著的变异性,这表明胞嘧啶甲基化的维持是一个动态过程;(ii)在所研究区域中非CpG胞嘧啶的甲基化可能会发生,但很少见;(iii)分析的脆性X男性中的甲基化镶嵌现象与正常女性中活性X和非活性X等位基因的甲基化镶嵌现象非常相似,这表明一些脆性X男性的甲基化镶嵌现象反映了正常女性中存在的FMR1表达的类似开启和关闭状态;(iv)脆性X等位基因上的高甲基化比女性正常非活性X等位基因上的高甲基化略为明显;(v)在相隔5年对脆性X男性进行采样的期间,低甲基化和高甲基化等位基因的总体二分法持续存在;(vi)甲基化变异性在α-PAL转录因子的共有结合序列处最为明显,该序列可能在调节FMR1的表达中起作用。

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