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Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci

Authors :
D’haene, Eva
López-Soriano, Víctor
Martínez-García, Pedro Manuel
Kalayanamontri, Soraya
Rey, Alfredo Dueñas
Sousa-Ortega, Ana
Naranjo, Silvia
Van de Sompele, Stijn
Vantomme, Lies
Mahieu, Quinten
Vergult, Sarah
Neto, Ana
Gómez-Skarmeta, José Luis
Martínez-Morales, Juan Ramón
Bauwens, Miriam
Tena, Juan Jesús
De Baere, Elfride
Source :
Genome Biology; December 2024, Vol. 25 Issue: 1
Publication Year :
2024

Abstract

Background: Vision depends on the interplay between photoreceptor cells of the neural retina and the underlying retinal pigment epithelium (RPE). Most genes involved in inherited retinal diseases display specific spatiotemporal expression within these interconnected retinal components through the local recruitment of cis-regulatory elements (CREs) in 3D nuclear space. Results: To understand the role of differential chromatin architecture in establishing tissue-specific expression at inherited retinal disease loci, we mapped genome-wide chromatin interactions using in situ Hi-C and H3K4me3 HiChIP on neural retina and RPE/choroid from human adult donor eyes. We observed chromatin looping between active promoters and 32,425 and 8060 candidate CREs in the neural retina and RPE/choroid, respectively. A comparative 3D genome analysis between these two retinal tissues revealed that 56% of 290 known inherited retinal disease genes were marked by differential chromatin interactions. One of these was ABCA4, which is implicated in the most common autosomal recessive inherited retinal disease. We zoomed in on retina- and RPE-specific cis-regulatory interactions at the ABCA4locus using high-resolution UMI-4C. Integration with bulk and single-cell epigenomic datasets and in vivo enhancer assays in zebrafish revealed tissue-specific CREs interacting with ABCA4. Conclusions: Through comparative 3D genome mapping, based on genome-wide, promoter-centric, and locus-specific assays of human neural retina and RPE, we have shown that gene regulation at key inherited retinal disease loci is likely mediated by tissue-specific chromatin interactions. These findings do not only provide insight into tissue-specific regulatory landscapes at retinal disease loci, but also delineate the search space for non-coding genomic variation underlying unsolved inherited retinal diseases. Graphical Abstract: <fig id="Figa" position="anchor"> <graphic position="anchor" specific-use="HTML" mime-subtype="PNG" href="MediaObjects/13059_2024_3250_Figa_HTML.png" id="MO1"></graphic> </fig>

Details

Language :
English
ISSN :
14747596 and 1474760X
Volume :
25
Issue :
1
Database :
Supplemental Index
Journal :
Genome Biology
Publication Type :
Periodical
Accession number :
ejs66406031
Full Text :
https://doi.org/10.1186/s13059-024-03250-6