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Title: Snai1-driven sequential emt changes attributed by selective chromatin enrichment of RAD21 and GRHL2
Authors: Sundararajan, V. 
Tan, M.
Tan, T.Z. 
Pang, Q.Y. 
Ye, J.
Chung, V.Y. 
Huang, R.Y.-J. 
Keywords: Chromatin looping
EMT spectrum
Issue Date: 2020
Publisher: MDPI AG
Citation: Sundararajan, V., Tan, M., Tan, T.Z., Pang, Q.Y., Ye, J., Chung, V.Y., Huang, R.Y.-J. (2020). Snai1-driven sequential emt changes attributed by selective chromatin enrichment of RAD21 and GRHL2. Cancers 12 (5) : 1140. ScholarBank@NUS Repository.
Rights: Attribution 4.0 International
Abstract: Over two decades of research on cancer-associated epithelial-mesenchymal transition (EMT) led us to ascertain the occurrence of transitional intermediate states (collectively referred to as the EMT spectrum). Among the molecular factors that drive EMT, SNAI1 plays an indispensable role in regulating other core transcription factors, and this regulation is highly context-dependent. However, molecular investigation on this context-dependent regulation is still lacking. Using two ovarian cancer cell lines, we show that SNAI1 regulation on other core EMT-TFs switches from a repressive control in highly epithelial cells to an activation signaling in intermediate epithelial cells. Upon further scrutiny, we identify that the expression of early epithelial genes PERP and ERBB3 are differentially regulated in SNAI1-induced sequential EMT changes. Mechanistically, we show that changes in PERP and ERBB3 transcript levels could be correlated to the selective enrichment loss of RAD21, a cohesin component, at the distal enhancer sites of PERP and ERBB3, which precedes that of the proximal promoter-associated sites. Furthermore, the RAD21 enrichment at the distal enhancer sites is dependent on GRHL2 expression. In a nutshell, the alteration of GRHL2-associated RAD21 enrichment in epithelial genes is crucial to redefine the transition of cellular states along the EMT spectrum. @ 2020 by the authors. Licensee MDPI, Basel, Switzerland.
Source Title: Cancers
ISSN: 2072-6694
DOI: 10.3390/cancers12051140
Rights: Attribution 4.0 International
Appears in Collections:Staff Publications

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