Regions of focal DNA hypermethylation and long-range hypomethylation in colorectal cancer coincide with nuclear laminag-associated domains

Benjamin P. Berman, Daniel J. Weisenberger, Joseph F. Aman, Toshinori Hinoue, Zachary Ramjan, Yaping Liu, Houtan Noushmehr, Christopher P.E. Lange, Cornelis M. Van Dijk, Rob A.E.M. Tollenaar, David Van Den Berg, Peter W. Laird*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

511 Scopus citations

Abstract

Extensive changes in DNA methylation are common in cancer and may contribute to oncogenesis through transcriptional silencing of tumor-suppressor genes. Genome-scale studies have yielded important insights into these changes but have focused on CpG islands or gene promoters. We used whole-genome bisulfite sequencing (bisulfite-seq) to comprehensively profile a primary human colorectal tumor and adjacent normal colon tissue at single-basepair resolution. Regions of focal hypermethylation in the tumor were located primarily at CpG islands and were concentrated within regions of long-range (>100 kb) hypomethylation. These hypomethylated domains covered nearly half of the genome and coincided with late replication and attachment to the nuclear lamina in human cell lines. We confirmed the confluence of hypermethylation and hypomethylation within these domains in 25 diverse colorectal tumors and matched adjacent tissue. We propose that widespread DNA methylation changes in cancer are linked to silencing programs orchestrated by the three-dimensional organization of chromatin within the nucleus.

Original languageEnglish (US)
Pages (from-to)40-46
Number of pages7
JournalNature Genetics
Volume44
Issue number1
DOIs
StatePublished - Jan 2012

ASJC Scopus subject areas

  • Genetics

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