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ATAC-Seq analysis reveals a widespread decrease of chromatin accessibility in age-related macular degeneration
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Abstract
Age-related macular degeneration (AMD) is a significant cause of vision loss in the elderly. The extent to which epigenetic changes regulate AMD progression is unclear. Here we globally profile chromatin accessibility using ATAC-Seq in the retina and retinal pigmented epithelium (RPE) from AMD and control patients. Global decreases in chromatin accessibility occur in the RPE with early AMD, and in the retina of advanced disease, suggesting that dysfunction in the RPE drives disease onset. Footprints of photoreceptor and RPE-specific transcription factors are enriched in differentially accessible regions (DARs). Genes associated with DARs show altered expression in AMD. Cigarette smoke treatment of RPE cells recapitulates chromatin accessibility changes seen in AMD, providing an epigenetic link between a known risk factor for AMD and AMD pathology. Finally, overexpression of HDAC11 is partially responsible for the observed reduction in chromatin accessibility, suggesting that HDAC11 may be a potential new therapeutic target for AMD.
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“which aligns with the conclusion that chromatin accessibility alterations occur in age-related macular degeneration54.”
From Inferring gene regulatory networks from single-cell multiome data using atlas-scale external data (2025) · cites this paper as [54]
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Age‐related dysregulation of the retinal transcriptome in African turquoise killifish
Bergmans, S., Noel, N. C. L., Masin, L., Harding, E. G., Krzywańska, A. M., Schutter, J. D. D., Ayana, R., Hu, C., Arckens, L., Ruzycki, P. A., et al. (2024) · Aging Cell · doi:10.1111/acel.14192 · Cited by 17
van Karnebeek, C., O’Donnell‐Luria, A., Baynam, G. S., Baudot, A., Groza, T., Jans, J. J. M., Lassmann, T., Letinturier, M. C. V., Montgomery, S. B., Robinson, P. N., et al. (2024) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-024-03361-0 · Cited by 21
Montaser, A. B., Gao, F., Peters, D. L., Vainionpää, K., Zhibin, N., Skowronska‐Krawczyk, D., Figeys, D., Palczewski, K., & Leinonen, H. (2024) · Molecular & Cellular Proteomics · doi:10.1016/j.mcpro.2024.100855 · Cited by 16
Wang, Z., Huang, Y., Chu, F., Liao, K., Cui, Z., Chen, J., & Tang, S. (2021) · Bioengineered · doi:10.1080/21655979.2021.1976502 · Cited by 17
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
Quinodoz, M., Rodenburg, K., Cvačková, Z., Kamińska, K., de Bruijn, S. E., Iglesias-Romero, A. B., Boonen, E. G. M., Ullah, M., Zomer, N., Folcher, M., et al. (2026) · Nature Genetics · doi:10.1038/s41588-025-02451-4 · Cited by 32
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De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosaPreprint
Quinodoz, M., Rodenburg, K., Cvačková, Z., Kamińska, K., de Bruijn, S. E., Iglesias-Romero, A. B., Boonen, E. G. M., Ullah, M., Zomer, N., Folcher, M., et al. (2025) · medRxiv · doi:10.1101/2025.01.06.24317169 · Cited by 15
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Self-citationEpigenetics and Degenerative Retinal Diseases: Prospects for New Therapeutic Approaches
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Self-citationBuilding a Mammalian Retina: An Eye on Chromatin Structure
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Age- and sex- divergent translatomic responses of the mouse retinal pigmented epithelium
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Self-citationNovel Epigenetic Clock Biomarkers of Age-Related Macular Degeneration
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Metadata
- Authors
- Wang, J., Zibetti, C., Shang, P., Sripathi, S. R., Zhang, P., Cano, M., Hoang, T., Xia, S., Ji, H., Merbs, S. L., Zack, D. J., Handa, J. T., Sinha, D., Blackshaw, S., & Qian, J.
- Affiliations
- Johns Hopkins University (US)
- Corresponding author
- Blackshaw, Seth
- Qian, Jiang
- ORCID
- Venue
- Nature Communications
- Published
- 2018-04-10
- Volume
- 9
- Issue
- 1
- Pages
- 1364-1364
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC5893535
- OpenAlex
- W2797486746
- Cited by
- 185
- References
- 74
- Citations by year
- 2026: 15 · 2025: 27 · 2024: 32 · 2023: 24 · 2022: 24 · 2021: 24 · 2020: 21 · 2019: 13 · 2018: 5
- FWCI
- 17.10
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- NORA - Norwegian Open Research Archives (submittedVersion, cc-by)
- Funders
- International Retinal Research Foundation
- National Institutes of Health
- National Eye Institute (R01EY020560, R01EY024580, R01EY023188, R01EY027691)
- National Institute of Neurological Disorders and Stroke (R01NS091165)
- Topics
- Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
- Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- age-related macular degeneration, chromatin accessibility, retinal pigment epithelium, retina, epigenetic regulation, differentially accessible regions, cigarette smoke, HDAC11, histone deacetylase, therapeutic target
- MeSH terms
- Aged, Aged, 80 and over, Chromatin, Epithelial Cells, Eye Proteins, Female, Histone Deacetylases, Humans, Macular Degeneration, Male, Smoke, Nicotiana, Transcription Factors, Case-Control Studies, Epigenesis, Genetic, Complex Mixtures, Genome-Wide Association Study, Retinal Pigment Epithelium, High-Throughput Nucleotide Sequencing, Primary Cell Culture
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