中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
An improved method for genome wide dna methylation profiling correlated to transcription and genomic instability in two breast cancer cell lines

文献类型:期刊论文

作者Li, Jian1,7; Gao, Fei1,2,3,4; Li, Ning2,3; Li, Shengting1; Yin, Guangliang3; Tian, Geng2,3; Jia, Shangang2,3; Wang, Kai1,5,7; Zhang, Xiuqing2,3; Yang, Huanming6
刊名Bmc genomics
出版日期2009-05-13
卷号10页码:15
ISSN号1471-2164
DOI10.1186/1471-2164-10-223
通讯作者Li, jian(jianl@humgen.au.dk)
英文摘要Background: dna methylation is a widely studied epigenetic mechanism known to correlate with gene repression and genomic stability. development of sensitive methods for global detection of dna methylation events is of particular importance. results: we here describe a technique, called modified methylation-specific digital karyotyping (mmsdk) based on methylation-specific digital karyotyping (msdk) with a novel sequencing approach. briefly, after a tandem digestion of genomic dna with a methylation-sensitive mapping enzyme and a fragmenting enzyme, short sequence tags are obtained. these tags are amplified, followed by direct, massively parallel sequencing (solexa 1g genome analyzer). this method allows high-throughput and low-cost genome-wide dna methylation mapping. we applied this method to investigate global dna methylation profiles for widely used breast cancer cell lines, mcf-7 and mda-mb-231, which are representatives for luminal-like and mesenchymal-like cancer types, respectively. by comparison, a highly similar overall dna methylation pattern was revealed for the two cell lines. however a cohort of individual genomic loci with significantly different dna methylation status between two cell lines was identified. furthermore, we revealed a genome-wide significant correlation between gene expression and the methylation status of gene promoters with cpg islands (cgis) in the two cancer cell lines, and a correlation of gene expression and the methylation status of promoters without cgis in mcf-7 cells. conclusion: the mmsdk method will be a valuable tool to increase the current knowledge of genome wide dna methylation profiles.
WOS关键词GENE-EXPRESSION ; HYPOMETHYLATION ; TUMORS ; HYBRIDIZATION ; CARCINOMAS ; SUBCLASSES ; SITES
WOS研究方向Biotechnology & Applied Microbiology ; Genetics & Heredity
WOS类目Biotechnology & Applied Microbiology ; Genetics & Heredity
语种英语
WOS记录号WOS:000267735100001
出版者BIOMED CENTRAL LTD
URI标识http://www.irgrid.ac.cn/handle/1471x/2399447
专题中国科学院大学
通讯作者Li, Jian
作者单位1.Univ Aarhus, Inst Human Genet, DK-8000 Aarhus C, Denmark
2.Chinese Acad Sci, Beijing Inst Genom, Beijing 101300, Peoples R China
3.Beijing Genom Inst, Shenzhen 518083, Guangdong, Peoples R China
4.Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
5.Univ Aarhus, BiRC, DK-8000 Aarhus, Denmark
6.Beijing Genom Inst, Beijing 101300, Peoples R China
7.Danish Ctr Translat Breast Canc Res DCTB, DK-2100 Copenhagen, Denmark
推荐引用方式
GB/T 7714
Li, Jian,Gao, Fei,Li, Ning,et al. An improved method for genome wide dna methylation profiling correlated to transcription and genomic instability in two breast cancer cell lines[J]. Bmc genomics,2009,10:15.
APA Li, Jian.,Gao, Fei.,Li, Ning.,Li, Shengting.,Yin, Guangliang.,...&Bolund, Lars.(2009).An improved method for genome wide dna methylation profiling correlated to transcription and genomic instability in two breast cancer cell lines.Bmc genomics,10,15.
MLA Li, Jian,et al."An improved method for genome wide dna methylation profiling correlated to transcription and genomic instability in two breast cancer cell lines".Bmc genomics 10(2009):15.

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来源:中国科学院大学

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