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

(2024) GENOME BIOLOGY. 25(1).
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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 ABCA4 locus 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.
Keywords
Enhancer assay, Cis-regulatory element (CRE), ABCA4, Inherited retinal disease (IRD), Retinal pigment epithelium (RPE), Neural retina, UMI-4C, Hi-C, 3D genome structure, HiChIP

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MLA
D’haene, Eva, et al. “Comparative 3D Genome Analysis between Neural Retina and Retinal Pigment Epithelium Reveals Differential Cis-Regulatory Interactions at Retinal Disease Loci.” GENOME BIOLOGY, vol. 25, no. 1, 2024, doi:10.1186/s13059-024-03250-6.
APA
D’haene, E., Lopez Soriano, V., Martínez-García, P. M., Kalayanamontri, S., Dueñas Rey, A., Sousa-Ortega, A., … De Baere, E. (2024). Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci. GENOME BIOLOGY, 25(1). https://doi.org/10.1186/s13059-024-03250-6
Chicago author-date
D’haene, Eva, Victor Lopez Soriano, Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey, Ana Sousa-Ortega, Silvia Naranjo, et al. 2024. “Comparative 3D Genome Analysis between Neural Retina and Retinal Pigment Epithelium Reveals Differential Cis-Regulatory Interactions at Retinal Disease Loci.” GENOME BIOLOGY 25 (1). https://doi.org/10.1186/s13059-024-03250-6.
Chicago author-date (all authors)
D’haene, Eva, Victor Lopez Soriano, Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey, Ana Sousa-Ortega, Silvia Naranjo, Stijn Van de Sompele, Lies Vantomme, Quinten Mahieu, Sarah Vergult, Ana Neto, José Luis Gómez-Skarmeta, Juan Ramón Martínez-Morales, Miriam Bauwens, Juan Jesús Tena, and Elfride De Baere. 2024. “Comparative 3D Genome Analysis between Neural Retina and Retinal Pigment Epithelium Reveals Differential Cis-Regulatory Interactions at Retinal Disease Loci.” GENOME BIOLOGY 25 (1). doi:10.1186/s13059-024-03250-6.
Vancouver
1.
D’haene E, Lopez Soriano V, Martínez-García PM, Kalayanamontri S, Dueñas Rey A, Sousa-Ortega A, et al. Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci. GENOME BIOLOGY. 2024;25(1).
IEEE
[1]
E. D’haene et al., “Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci,” GENOME BIOLOGY, vol. 25, no. 1, 2024.
@article{01HYMRNDX2V90R0AH8C5PPAT81,
  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 ABCA4 locus 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.
             }},
  articleno    = {{123}},
  author       = {{D'haene, Eva and Lopez Soriano, Victor and Martínez-García, Pedro Manuel and Kalayanamontri, Soraya and Dueñas Rey, Alfredo and Sousa-Ortega, Ana and Naranjo, Silvia and Van de Sompele, Stijn and Vantomme, Lies and Mahieu, Quinten and Vergult, Sarah and Neto, Ana and Gómez-Skarmeta, José Luis and Martínez-Morales, Juan Ramón and Bauwens, Miriam and Tena, Juan Jesús and De Baere, Elfride}},
  issn         = {{1474-760X}},
  journal      = {{GENOME BIOLOGY}},
  keywords     = {{Enhancer assay,Cis-regulatory element (CRE),ABCA4,Inherited retinal disease (IRD),Retinal pigment epithelium (RPE),Neural retina,UMI-4C,Hi-C,3D genome structure,HiChIP}},
  language     = {{eng}},
  number       = {{1}},
  pages        = {{24}},
  title        = {{Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci}},
  url          = {{http://doi.org/10.1186/s13059-024-03250-6}},
  volume       = {{25}},
  year         = {{2024}},
}

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