Comparative genomics identification of a novel set of temporally regulated hedgehog target genes in the retina

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• 作者：Brian McNeill^a ; ^c ; ^d ; Carol Perez-Iratxeta^b ; Chantal Mazerolle^a ; ^c ; ^d ; Marosh Furimsky^a ; Yuji Mishina^f ; ^g ; Miguel A. Andrade-Navarro^e ; Valerie A. Wallace^a ; ^c ; ^d ; ^{vwallace@ohri.ca}
• 关键词：Hedgehog ; Gli transcription factors ; Development ; Progenitor cells ; Retina
• 刊名：Molecular and Cellular Neuroscience
• 出版年：2012
• 期刊代码：173_10447431
• 类别：bio
• 出版时间：March, 2012
• 卷：49
• 期：3
• 页码：333-340
• 文件大小：743 K

摘要

The hedgehog (Hh) signaling pathway is involved in numerous developmental and adult processes with many links to cancer. In vertebrates, the activity of the Hh pathway is mediated primarily through three Gli transcription factors (Gli1, 2 and 3) that can serve as transcriptional activators or repressors. The identification of Gli target genes is essential for the understanding of the Hh-mediated processes. We used a comparative genomics approach using the mouse and human genomes to identify 390 genes that contained conserved Gli binding sites. RT-qPCR validation of 46 target genes in E14.5 and P0.5 retinal explants revealed that Hh pathway activation resulted in the modulation of 30 of these targets, 25 of which demonstrated a temporal regulation. Further validation revealed that the expression of Bok, FoxA1, Sox8 and Wnt7a was dependent upon Sonic Hh (Shh) signaling in the retina and their regulation is under positive and negative controls by Gli2 and Gli3, respectively. We also show using chromatin immunoprecipitation that Gli2 binds to the Sox8 promoter, suggesting that Sox8 is an Hh-dependent direct target of Gli2. Finally, we demonstrate that the Hh pathway also modulates the expression of Sox9 and Sox10, which together with Sox8 make up the SoxE group. Previously, it has been shown that Hh and SoxE group genes promote M眉ller glial cell development in the retina. Our data are consistent with the possibility for a role of SoxE group genes downstream of Hh signaling on M眉ller cell development.