PAX6 Isoforms, along with Reprogramming Factors, Differentially Regulate the Induction of Cornea-specific Genes

Yuzuru Sasamoto(The University of Osaka), Ryuhei Hayashi(The University of Osaka), Sung‐Joon Park(The University of Tokyo), Mihoko Saito-Adachi(National Cancer Centre Japan), Yutaka Suzuki(The University of Tokyo), Satoshi Kawasaki(The University of Osaka), Andrew J. Quantock(Cardiff University), Kenta Nakai(The University of Tokyo), Motokazu Tsujikawa(The University of Osaka), Kohji Nishida(The University of Osaka)
Scientific Reports
February 22, 2016
Cited by 54Open Access
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Abstract

PAX6 is the key transcription factor involved in eye development in humans, but the differential functions of the two PAX6 isoforms, isoform-a and isoform-b, are largely unknown. To reveal their function in the corneal epithelium, PAX6 isoforms, along with reprogramming factors, were transduced into human non-ocular epithelial cells. Herein, we show that the two PAX6 isoforms differentially and cooperatively regulate the expression of genes specific to the structure and functions of the corneal epithelium, particularly keratin 3 (KRT3) and keratin 12 (KRT12). PAX6 isoform-a induced KRT3 expression by targeting its upstream region. KLF4 enhanced this induction. A combination of PAX6 isoform-b, KLF4, and OCT4 induced KRT12 expression. These new findings will contribute to furthering the understanding of the molecular basis of the corneal epithelium specific phenotype.


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