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PMID: 16444255 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Evidence for an instructive mechanism of de novo methylation in cancer cells.

Nature genetics ·Vol. 38 ·No. 2 ·2006-02-00 ·Pages 149-53

Keshet I, Schlesinger Y, Farkash S, Rand E, Hecht M, Segal E, Pikarski E, Young RA, Niveleau A, Cedar H, Simon I

Abstract

DNA methylation has a role in the regulation of gene expression during normal mammalian development but can also mediate epigenetic silencing of CpG island genes in cancer and other diseases. Many individual genes (including tumor suppressors) have been shown to undergo de novo methylation in specific tumor types, but the biological logic inherent in this process is not understood. To decipher this mechanism, we have adopted a new approach for detecting CpG island DNA methylation that can be used together with microarray technology. Genome-wide analysis by this technique demonstrated that tumor-specific methylated genes belong to distinct functional categories, have common sequence motifs in their promoters and are found in clusters on chromosomes. In addition, many are already repressed in normal cells. These results are consistent with the hypothesis that cancer-related de novo methylation may come about through an instructive mechanism.

MeSH Terms
Animals Chromosomes/genetics Computational Biology DNA Methylation Gene Expression Regulation, Neoplastic Genome Models, Genetic Neoplasms/genetics,pathology
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Keshet Ilana
Department of Cellular Biochemistry and Human Genetics, Hebrew University, Jerusalem, Israel.
Schlesinger Yeshayahu
Farkash Shlomit
Rand Eyal
Hecht Merav
Segal Eran
Pikarski Eli
Young Richard A
Niveleau Alain
Cedar Howard
Simon Itamar
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
2006-02-00
Pages
149-53
Language
English
Region
United States
NLM ID
9216904
Subset
IM
Grants
NHGRI NIH HHS · R01 HG002668 · United States
NHGRI NIH HHS · R01 HG002668-03 · United States
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