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Comparative isoschizomer profiling of cytosine methylation: The HELP assay
Author(s) -
Batbayar Khulan,
Reid F. Thompson,
Kenny Ye,
Melissa Fazzari,
Masako Suzuki,
Edyta Stasiek,
María E. Figueroa,
Jacob L. Glass,
Quan Chen,
Cristina Montagna,
Eli Hatchwell,
Rebecca R. Selzer,
Todd Richmond,
Roland D. Green,
Ari Melnick,
John M. Greally
Publication year - 2006
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.5273806
Subject(s) - biology , dna methylation , hpaii , differentially methylated regions , cpg site , methylation , illumina methylation assay , cytosine , genetics , methylated dna immunoprecipitation , pyrosequencing , genome , isoschizomer , gene , promoter , microbiology and biotechnology , bisulfite sequencing , gene expression
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.

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