Densely methylated sequences that are preferentially localized at telomere-proximal regions of human chromosomes

被引:63
作者
Brock, GJR
Charlton, J
Bird, A
机构
[1] Univ Edinburgh, Inst Cell & Mol Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[2] Univ Glasgow, Div Mol Genet, Inst Biomed & Life Sci, Glasgow G11 6NU, Lanark, Scotland
基金
英国惠康基金;
关键词
CpG methylation; subtelomeric;
D O I
10.1016/S0378-1119(99)00442-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have constructed a library of densely methylated DNA sequences from human blood DNA by selecting fragments with a high affinity for a methyl-CpG binding domain (MBD) column. PCR analysis of the library confirmed the presence of known densely methylated CpG island sequences. Analysis of random clones, however, showed that the library was dominated by sequences whose G+C content and CpG frequency were intermediate between those of bulk genomic DNA and bona fide CpG islands. When human chromosomes were probed with the library by fluorescent in situ hybridisation (FISH), the predominant sites of labelling were at terminal regions of many chromosomes, approximately corresponding to T-bands. Analysis of the methylation status of random clones indicated that all were heavily methylated at CpGs in blood DNA, but many were undermethylated in sperm DNA, Lack of methylation in germ cells may reduce CpG depletion at some sub-terminal sequences and result in a high density of methyl-CpG when these regions become methylated in somatic cells. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:269 / 277
页数:9
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