A multifactorial signature of DNA sequence and polycomb binding predicts aberrant CpG island methylation.
Ontology highlight
ABSTRACT: Aberrant CpG island methylation is associated with transcriptional silencing of regulatory genes in human cancer. Although most CpG islands remain unmethylated, a subset accrues aberrant methylation in cancer via unknown mechanisms. Previously, we showed that CpG islands differ in their intrinsic propensity towards hypermethylation. We developed a classifier (PatMAn) based on the frequencies of seven DNA sequence patterns that discriminated methylation-prone (MP) and methylation-resistant (MR) CpG islands. Here, we report on the genome-wide application and direct testing of PatMAn in cancer. Although trained on data from a cell culture model of de novo methylation involving the overexpression of DNMT1, PatMAn accurately predicted CpG islands at increased risk of hypermethylation in cancer
SUBMITTER: McCabe MT
PROVIDER: S-EPMC2653261 | biostudies-literature | 2009 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA