Regulation of beta 4-integrin expression by epigenetic modifications in the mammary gland and during the epithelial-to-mesenchymal transition
UMass Chan Affiliations
Department of Cancer BiologyDocument Type
Journal ArticlePublication Date
2009-06-25Keywords
AnimalsCadherins
Cell Line
Cell Transdifferentiation
CpG Islands
*DNA Methylation
Epithelial Cells
Female
Histones
Integrin beta4
Mammary Glands, Animal
Mesoderm
Mice
Mice, Transgenic
Promoter Regions, Genetic
Transcriptional Activation
Transforming Growth Factor beta
Life Sciences
Medicine and Health Sciences
Metadata
Show full item recordAbstract
The beta 4 integrin is expressed in epithelial cells, a few other cell types and in some carcinomas. Despite this restricted expression pattern and the functional importance of beta 4 integrin in epithelial and carcinoma biology, little is known about how its expression is regulated. Here, we assessed the epigenetic regulation of beta 4 integrin based on the presence of a large CpG island in the beta 4-integrin gene promoter. We separated basal (beta 4+) and luminal (beta 4-) epithelial cells from the mammary glands of K14-eGFP mice and demonstrated that the beta 4-integrin promoter is unmethylated in basal cells and methylated in luminal cells. We also observed that expression of beta 4 integrin and E-cadherin is lost during the epithelial-to-mesenchymal transition (EMT) of mammary gland cells induced by transforming growth factor beta (TGFbeta), which is coincident with de novo DNA methylation, a decrease in active histone modifications (H3K9Ac and H3K4me3) and an increase in the repressive histone modification H3K27me3. Furthermore, TGFbeta withdrawal promotes a mesenchymal-to-epithelial transition (MET) and triggers the re-expression of beta 4 integrin and E-cadherin. Intriguingly, demethylation at either promoter is not obligatory for transcriptional reactivation after TGFbeta withdrawal. However, both H3K9Ac and H3K4me3 modifications are restored during the MET, and H3K27me3 is reduced, strongly suggesting that reversible histone modifications rather than DNA demethylation are the predominant factors in reactivating expression of these genes. Our data indicate that complex epigenetic modifications contribute to the regulation of the beta 4 integrin and E-cadherin.Source
J Cell Sci. 2009 Jul 15;122(Pt 14):2473-80. Epub 2009 Jun 23. Link to article on publisher's site
DOI
10.1242/jcs.049148Permanent Link to this Item
http://hdl.handle.net/20.500.14038/39353PubMed ID
19549682Related Resources
ae974a485f413a2113503eed53cd6c53
10.1242/jcs.049148