DNA Hypermethylation Encroachment at CpG Island Borders in Cancer Is Predisposed by H3K4 Monomethylation Patterns.
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BORIS DOI
Date of Publication
February 11, 2019
Publication Type
Article
Division/Institute
Contributor
Skvortsova, Ksenia | |
Masle-Farquhar, Etienne | |
Luu, Phuc-Loi | |
Song, Jenny Z | |
Qu, Wenjia | |
Zotenko, Elena | |
Gould, Cathryn M | |
Du, Qian | |
Peters, Timothy J | |
Colino-Sanguino, Yolanda | |
Pidsley, Ruth | |
Nair, Shalima S | |
Khoury, Amanda | |
Smith, Grady C | |
Miosge, Lisa A | |
Reed, Joanne H | |
Kench, James G | |
Horvath, Lisa | |
Bogdanovic, Ozren | |
Lim, Sue Mei | |
Polo, Jose M | |
Goodnow, Christopher C | |
Stirzaker, Clare | |
Clark, Susan J |
Subject(s)
Series
Cancer cell
ISSN or ISBN (if monograph)
1535-6108
Publisher
Cell Press
Language
English
Publisher DOI
PubMed ID
30753827
Uncontrolled Keywords
Description
Promoter CpG islands are typically unmethylated in normal cells, but in cancer a proportion are subject to hypermethylation. Using methylome sequencing we identified CpG islands that display partial methylation encroachment across the 5' or 3' CpG island borders. CpG island methylation encroachment is widespread in prostate and breast cancer and commonly associates with gene suppression. We show that the pattern of H3K4me1 at CpG island borders in normal cells predicts the different modes of cancer CpG island hypermethylation. Notably, genetic manipulation of Kmt2d results in concordant alterations in H3K4me1 levels and CpG island border DNA methylation encroachment. Our findings suggest a role for H3K4me1 in the demarcation of CpG island methylation borders in normal cells, which become eroded in cancer.
File(s)
File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
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1-s2.0-S1535610819300388-main.pdf | text | Adobe PDF | 8.94 MB | publisher | published |