Cell-Type Specific DNA Methylation Patterns Define Human Breast Cellular Identity

被引:17
作者
Novak, Petr [1 ,4 ]
Stampfer, Martha R. [1 ,3 ]
Munoz-Rodriguez, Jose L. [1 ,2 ]
Garbe, James C. [3 ]
Ehrich, Mathias [5 ]
Futscher, Bernard W. [1 ,2 ]
Jensen, Taylor J. [1 ,2 ,6 ]
机构
[1] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85721 USA
[2] Univ Arizona, Coll Pharm, Dept Pharmacol & Toxicol, Tucson, AZ 85721 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Life Sci, Berkeley, CA 94720 USA
[4] Acad Sci Czech Republ, Inst Plant Mol Biol, Vvi, Biol Ctr ASCR, CR-37005 Ceske Budejovice, Czech Republic
[5] Sequenom Inc, San Diego, CA USA
[6] John Hopkins Ct, Sequenom Ctr Mol Med, San Diego, CA USA
来源
PLOS ONE | 2012年 / 7卷 / 12期
基金
美国国家卫生研究院;
关键词
MAMMARY EPITHELIAL-CELLS; DIFFERENTIAL METHYLATION; EPIGENETIC INACTIVATION; HYPERMETHYLATION; PLURIPOTENT; EXPRESSION; GROWTH; GENES; BARRIERS; CLUSTER;
D O I
10.1371/journal.pone.0052299
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA methylation plays a role in a variety of biological processes including embryonic development, imprinting, X-chromosome inactivation, and stem cell differentiation. Tissue specific differential methylation has also been well characterized. We sought to extend these studies to create a map of differential DNA methylation between different cell types derived from a single tissue. Using three pairs of isogenic human mammary epithelial and fibroblast cells, promoter region DNA methylation was characterized using MeDIP coupled to microarray analysis. Comparison of DNA methylation between these cell types revealed nearly three thousand cell-type specific differentially methylated regions (ctDMRs). MassARRAY was performed upon 87 ctDMRs to confirm and quantify differential DNA methylation. Each of the examined regions exhibited statistically significant differences ranging from 10-70%. Gene ontology analysis revealed the overrepresentation of many transcription factors involved in developmental processes. Additionally, we have shown that ctDMRs are associated with histone related epigenetic marks and are often aberrantly methylated in breast cancer. Overall, our data suggest that there are thousands of ctDMRs which consistently exhibit differential DNA methylation and may underlie cell type specificity in human breast tissue. In addition, we describe the pathways affected by these differences and provide insight into the molecular mechanisms and physiological overlap between normal cellular differentiation and breast carcinogenesis.
引用
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页数:9
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