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视黄酸调节的表观遗传标记确定为视杯形成所需的直接靶基因。

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

作者信息

Berenguer Marie, Duester Gregg

机构信息

Development, Aging, and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California, United States of America.

出版信息

bioRxiv. 2025 Jun 25:2025.06.24.661406. doi: 10.1101/2025.06.24.661406.

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 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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47e3/12262313/1e619d6f4247/nihpp-2025.06.24.661406v1-f0001.jpg

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