Berenguer Marie, Duester Gregg
Development, Aging, and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California, United States of America.
bioRxiv. 2025 Jun 25:2025.06.24.661406. doi: 10.1101/2025.06.24.661406.
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 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 -/- 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 that also has an RA response element (RARE) located near the RA-regulated H3K27ac mark, providing strong evidence that RA directly activates . In situ hybridization studies showed that -/- embryos exhibit a large decrease in eye expression. CRISPR/Cas9 knockout of resulted in a defect in optic cup formation, thus demonstrating that RA directly activates in order to stimulate this stage of eye development.
视黄酸(RA)是一种转录调控因子,它调节眼睛发育的多个方面,包括视泡内陷形成视杯,尽管此前尚未确定发挥这一作用的靶基因。由于基因敲除胚胎中RA合成的缺失会影响数千个基因的表达水平,因此需要一种不同的方法来鉴定直接受RA调控的基因。在这里,我们将用于表观遗传标记的染色质免疫沉淀测序(ChIP-seq)与来自野生型胚胎和视杯形成失败的基因敲除胚胎的眼组织RNA测序相结合。我们鉴定出少数几个基因,当缺乏RA时其表达下降,并且附近的表观遗传基因激活标记(H3K27ac)的存在也减少。其中一个这样的基因是 ,它在受RA调控的H3K27ac标记附近也有一个视黄酸反应元件(RARE),这有力地证明了RA直接激活 。原位杂交研究表明,基因敲除胚胎的眼睛 表达大幅下降。对 进行CRISPR/Cas9基因敲除导致视杯形成缺陷,从而证明RA直接激活 以刺激眼睛发育的这一阶段。