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人类11号染色体上CpG岛等位基因甲基化状态的综合分析:与21号染色体的比较。

A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 11q: comparison with chromosome 21q.

作者信息

Yamada Yoichi, Shirakawa Tomoyo, Taylor Todd D, Okamura Kohji, Soejima Hidenobu, Uchiyama Michiko, Iwasaka Tsuyoshi, Mukai Tsunehiro, Muramoto Ken-Ichiro, Sakaki Yoshiyuki, Ito Takashi

机构信息

Department of Information and Systems Engineering, Faculty of Engineering, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.

出版信息

DNA Seq. 2006 Aug;17(4):300-6. doi: 10.1080/10425170600886128.

DOI:10.1080/10425170600886128
PMID:17312950
Abstract

It was generally believed that autosomal CpG islands (CGIs) escape methylation. However, our comprehensive analysis of allelic methylation status of 149 CGIs on human chromosome 21q revealed that a sizable fraction of them are methylated on both alleles even in normal blood cells. Here, we performed a similar analysis of 656 CGIs on chromosome 11q, which is gene-rich in contrast with 21q. The results indicate that 11q contains less methylated CGIs, especially those with tandem repeats and those in the coding or 3'-untranslated regions (UTRs), than 21q. Thus, methylation status of CGIs may substantially differ from one chromosome to another.

摘要

人们普遍认为常染色体CpG岛(CGIs)不会发生甲基化。然而,我们对人类21号染色体上149个CGIs的等位基因甲基化状态进行的全面分析表明,即使在正常血细胞中,其中相当一部分在两个等位基因上都发生了甲基化。在这里,我们对11号染色体上的656个CGIs进行了类似分析,与21号染色体相比,11号染色体富含基因。结果表明,与21号染色体相比,11号染色体上甲基化的CGIs较少,尤其是那些具有串联重复的CGIs以及编码区或3'非翻译区(UTRs)中的CGIs。因此,CGIs的甲基化状态可能在不同染色体之间存在显著差异。

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A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 11q: comparison with chromosome 21q.人类11号染色体上CpG岛等位基因甲基化状态的综合分析:与21号染色体的比较。
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Factors to preserve CpG-rich sequences in methylated CpG islands.在甲基化的CpG岛中保留富含CpG序列的因素。
BMC Genomics. 2015 Feb 28;16(1):144. doi: 10.1186/s12864-015-1286-x.
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Correlating CpG islands, motifs, and sequence variants in human chromosome 21.关联人类 21 号染色体上的 CpG 岛、基序和序列变异。
BMC Genomics. 2011;12 Suppl 2(Suppl 2):S10. doi: 10.1186/1471-2164-12-S2-S10. Epub 2011 Jul 27.
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Highly efficient PCR assay to discriminate allelic DNA methylation status using whole genome amplification.使用全基因组扩增来区分等位基因DNA甲基化状态的高效PCR检测方法。
BMC Res Notes. 2011 Jun 10;4:179. doi: 10.1186/1756-0500-4-179.
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Developmental programming of CpG island methylation profiles in the human genome.人类基因组中CpG岛甲基化谱的发育编程
Nat Struct Mol Biol. 2009 May;16(5):564-71. doi: 10.1038/nsmb.1594. Epub 2009 Apr 19.