Comparative isoschizomer profiling of cytosine methylation: The HELP assay

被引:274
作者
Khulan, Batbayar
Thompson, Reid F.
Ye, Kenny
Fazzari, Melissa J.
Suzuki, Masako
Stasiek, Edyta
Figueroa, Maria E.
Glass, Jacob L.
Chen, Quan
Montagna, Cristina
Hatchwell, Eli
Selzer, Rebecca R.
Richmond, Todd A.
Green, Roland D.
Melnick, Ari
Greally, John M. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[4] Albert Einstein Coll Med, Dept Dev & Mol Biol, Bronx, NY 10461 USA
[5] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
[6] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11797 USA
[7] NimbleGen Syst Inc, Madison, WI 53711 USA
关键词
D O I
10.1101/gr.5273806
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
The distribution of cytosine methylation in 6.2 Mb of the mouse genome was tested using cohybridization of genomic representations from a methylation-sensitive restriction enzyme and its methylation-insensitive isoschizomer. This assay, termed HELP ( HpaII tiny fragment Enrichment by Ligation-mediated PCR), allows both intragenomic profiling and intergenomic comparisons of cytosine methylation. The intragenomic profile shows most of the genome to be contiguous methylated sequence with occasional clusters of hypomethylated loci, usually but not exclusively at promoters and CpG islands. Intergenomic comparison found marked differences in cytosine methylation between spermatogenic and brain cells, identifying 223 new candidate tissue-specific differentially methylated regions (T-DMRs). Bisulfite pyrosequencing confirmed the four candidates tested to be T-DMRs, while quantitative RT-PCR for two genes with T-DMRs located at their promoters showed the HELP data to be correlated with gene activity at these loci. The HELP assay is robust, quantitative, and accurate and is providing new insights into the distribution and dynamic nature of cytosine methylation in the genome.
引用
收藏
页码:1046 / 1055
页数:10
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