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FGF-induced Pea3 transcription factors program the genetic landscape for cell fate determination.

PUBLICATION: 
Journal Article
Authors: 
Garg A, Hannan A, Wang Q, Collins T, Teng S, Bansal M, Zhong J, Xu K, Zhang X.
Year Published: 
2018
Publisher: 
PLoS Genet. 2018 Sep 6;14(9):e1007660. doi: 10.1371/journal.pgen.1007660. [Epub ahead of print]
Identifiers: 
PMID: 30188892 | DOI: 10.1371/journal.pgen.1007660
Abstract on PubMed

Abstract

FGF signaling is a potent inducer of lacrimal gland development in the eye, capable of transforming the corneal epithelium into glandular tissues. Here, we show that genetic ablation of the Pea3 family of transcription factors not only disrupted the ductal elongation and branching of the lacrimal gland, but also biased the lacrimal gland epithelium toward an epidermal cell fate. Analysis of high-throughput gene expression and chromatin immunoprecipitation data revealed that the Pea3 genes directly control both the positive and negative feedback loops of FGF signaling. Importantly, Pea3 genes are also required to suppress aberrant Notch signaling which, if gone unchecked, can compromise lacrimal gland development by preventing the expression of both Sox and Six family genes. These results demonstrate that Pea3 genes are key FGF early response transcriptional factors, programing the genetic landscape for cell fate determination.

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