CpG Island microarray probe sequences derived from a physical library are representative of CpG Islands annotated on the human genome

被引:77
|
作者
Heisler, LE
Torti, D
Boutros, PC
Watson, J
Chan, C
Winegarden, N
Takahashi, M
Yau, P
Huang, THM
Farnham, PJ
Jurisica, I
Woodgett, JR
Bremner, R
Penn, LZ
Der, SD
机构
[1] Univ Toronto, Dept Lab Med & Pathobiol, Program Proteom & Bioinformat, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Ontario Canc Inst, Div Canc Genom & Proteom, Toronto, ON M5G 2M9, Canada
[3] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[4] Univ Toronto, Microrray Ctr, Toronto, ON M5G 2C4, Canada
[5] Ohio State Univ, Ctr Comprehens Canc, Dept Mol Virol Immunol & Med Genet, Human Canc Genet Program, Columbus, OH 43210 USA
[6] Univ Calif Davis, Dept Med Pharmacol & Toxicol, Davis, CA 95616 USA
[7] Univ Toronto, Dept Comp Sci, Toronto, ON M5S 2M9, Canada
[8] Ontario Canc Inst, Div Signaling Biol, Toronto, ON M5G 2M9, Canada
[9] Toronto Western Res Inst, Toronto, ON M5T 2S8, Canada
关键词
D O I
10.1093/nar/gki582
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An effective tool for the global analysis of both DNA methylation status and protein-chromatin interactions is a microarray constructed with sequences containing regulatory elements. One type of array suited for this purpose takes advantage of the strong association between CpG Islands ( CGIs) and gene regulatory regions. We have obtained 20 736 clones from a CGI Library and used these to construct CGI arrays. The utility of this library requires proper annotation and assessment of the clones, including CpG content, genomic origin and proximity to neighboring genes. Alignment of clone sequences to the human genome (UCSC hg17) identified 9595 distinct genomic loci; 64% were defined by a single clone while the remaining 36% were represented by multiple, redundant clones. Approximately 68% of the loci were located near a transcription start site. The distribution of these loci covered all 23 chromosomes, with 63% overlapping a bioinformatically identified CGI. The high representation of genomic CGI in this rich collection of clones supports the utilization of microarrays produced with this library for the study of global epigenetic mechanisms and protein chromatin interactions. A browsable database is available on-line to facilitate exploration of the CGIs in this library and their association with annotated genes or promoter elements.
引用
收藏
页码:2952 / 2961
页数:10
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