Retinoic acid-regulated epigenetic marks identify Alx1 as a direct target gene required for optic cup formation

Abstract

Retinoic acid (RA) is a transcriptional control agent that regulates several aspects of eye development including invagination of the optic vesicle to form the optic cup, although a target gene for this role has not been previously identified. As loss of RA synthesis in Rdh10 knockout embryos affects the expression levels of thousands of genes, a different approach is needed to identity genes that are directly regulated by RA. Here, we combined ChIP-seq for epigenetic marks with RNA-seq on eye tissue from wild-type embryos and Rdh10-/-embryos that exhibit failure in optic cup formation. We identified a small number of genes with decreased expression when RA is absent that also have decreased presence of a nearby epigenetic gene activation mark (H3K27ac). One such gene was Alx1 that also has an RA response element (RARE) located near the RA-regulated H3K27ac mark, providing strong evidence that RA directly activates Alx1. In situ hybridization studies showed that Rdh10-/-embryos exhibit a large decrease in eye Alx1 expression. CRISPR/Cas9 knockout of Alx1 resulted in a defect in optic cup formation, thus demonstrating that RA directly activates Alx1 in order to stimulate this stage of eye development. HighlightsO_LIThe RA requirement for optic cup formation was examined using Rdh10 knockout embryos. C_LIO_LIEye RNA-seq and ChIP-seq (H3K27ac) identified Alx1 as a potential RA target gene. C_LIO_LIAlx1 exhibits RA-regulated H3K27ac deposition near exon 1 associated with a nearby RARE. C_LIO_LIAlx1 knockout embryos display a misfolded optic cup with a ventral defect similar to Rdh10 KO. C_LI