GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development - PubMed (original) (raw)
. 2011 Aug 12;89(2):334-43.
doi: 10.1016/j.ajhg.2011.07.011.
David L Duffy, Gu Zhu, Jimmy Z Liu, Stuart Macgregor, Allan F McRae, Margaret J Wright, Richard A Sturm, David A Mackey, Grant W Montgomery, Nicholas G Martin, Sarah E Medland
Affiliations
- PMID: 21835309
- PMCID: PMC3155193
- DOI: 10.1016/j.ajhg.2011.07.011
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development
Mats Larsson et al. Am J Hum Genet. 2011.
Abstract
Human iris patterns are highly variable. The origins of this variation are of interest in the study of iris-related eye diseases and forensics, as well as from an embryological developmental perspective, with regard to their possible relationship to fundamental processes of neurodevelopment. We have performed genome-wide association scans on four iris characteristics (crypt frequency, furrow contractions, presence of peripupillary pigmented ring, and number of nevi) in three Australian samples of European descent. Both the discovery (n = 2121) and replication (n = 499 and 73) samples showed evidence for association between (1) crypt frequency and variants in the axonal guidance gene SEMA3A (p = 6.6 × 10(-11)), (2) furrow contractions and variants within the cytoskeleton gene TRAF3IP1 (p = 2.3 × 10(-12)), and (3) the pigmented ring and variants in the well-known pigmentation gene SLC24A4 (p = 7.6 × 10(-21)). These replicated findings individually accounted for around 1.5%-3% of the variance for these iris characteristics. Because both SEMA3A and TRAFIP1 are implicated in pathways that control neurogenesis, neural migration, and synaptogenesis, we also examined the evidence of enhancement among such genes, finding enrichment for crypts and furrows. These findings suggest that genes involved in normal neuronal pattern development may also influence tissue structures in the human iris.
Copyright © 2011 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.
Figures
Figure 1
Crypt Frequency Crypt frequency measures the degree of hypoplasia in the two top cell layers in the iris; i.e., the anterior border layer and the underlying stroma. The arrows indicate examples of crypt markings of interest in the iris tissue. The categories above depict (A) only parallel and/or densely packed curly fibers, (B) spots of wavy fibers and 1–3 shallow crypts, (C) at least four shallow crypts, (D) at least five marked crypts and/or a tissue texture that is more permeable than in category 3, (E) at least four large crypts that extend at least 2/3 of the distance between the collarette and the periphery of the iris.
Figure 2
Extension and Evenness of the Pigmented Ring The pigmented ring measures the amount of melanin that surrounds the pupil and distinguishes different shades of green and hazel eye color (91% of people judged to have a green or hazel eye color by a distant observer in this sample had a pigmented ring). The categories above depict (A) the absence of a pigmented ring; (B) an uneven pigmented ring, covering 18–348 degrees; (C) an even pigmented ring, covering > 348 degrees.
Figure 3
Distinction and Extension of Furrow Contractions Furrows manifest as the result of a tendency of the iris to fold in exactly the same location each time the iris adapts to different light conditions. They relate to the overall thickness and density of the iris (thicker irises have more extended furrows). The arrows indicate example of furrows on the iris. The categories above depict (A) the absence of furrows, or short furrows extending < 90 degrees; (B) furrows extending between 90 and 288 degrees; (C) distinct furrows, extending at least 288 degrees; (D) more marked furrows than in category 3, extending at least 324 degrees; (E) at least two concentric furrows, with a primary furrow of > 324 degrees and a second furrow of > 288 degrees.
Figure 4
Frequency of Iris Nevi Iris nevi are melanin accumulations on the anterior border layer. The arrows point to examples of iris nevi. The categories above depict (A) the absence of iris nevi, (B) at least one iris nevus, (C) at least three iris nevi, (D) at least five iris nevi.
Figure 5
Q-Q Plots for the 24,812 SNPs Located within the 219 Genes in the Krasnova et al. Set55 See Table S9 as well.
Similar articles
- Genetics of human iris colour and patterns.
Sturm RA, Larsson M. Sturm RA, et al. Pigment Cell Melanoma Res. 2009 Oct;22(5):544-62. doi: 10.1111/j.1755-148X.2009.00606.x. Epub 2009 Jul 8. Pigment Cell Melanoma Res. 2009. PMID: 19619260 Review. - Iris Pigmented Lesions: Unraveling the Genetic Basis of Iris Freckles and Nevi.
Boldu-Roig J, Sorli-Clemente E, Kuljuh-Causevic A, Loras A, Anton A, Martinez-Cadenas C. Boldu-Roig J, et al. Invest Ophthalmol Vis Sci. 2025 Apr 1;66(4):62. doi: 10.1167/iovs.66.4.62. Invest Ophthalmol Vis Sci. 2025. PMID: 40261663 Free PMC article. - A Genome-Wide Association Study of Skin and Iris Pigmentation among Individuals of South Asian Ancestry.
Jonnalagadda M, Faizan MA, Ozarkar S, Ashma R, Kulkarni S, Norton HL, Parra E. Jonnalagadda M, et al. Genome Biol Evol. 2019 Apr 1;11(4):1066-1076. doi: 10.1093/gbe/evz057. Genome Biol Evol. 2019. PMID: 30895295 Free PMC article. - Genetic correlations among texture characteristics in the human iris.
Larsson M, Pedersen NL. Larsson M, et al. Mol Vis. 2004 Nov 2;10:821-31. Mol Vis. 2004. PMID: 15534585 - Molecular and biochemical mechanisms of human iris color: A comprehensive review.
Dorgaleleh S, Naghipoor K, Barahouie A, Dastaviz F, Oladnabi M. Dorgaleleh S, et al. J Cell Physiol. 2020 Dec;235(12):8972-8982. doi: 10.1002/jcp.29824. Epub 2020 Jun 2. J Cell Physiol. 2020. PMID: 32488945 Review.
Cited by
- Genes associated with Alzheimer's disease: an overview and current status.
Giri M, Zhang M, Lü Y. Giri M, et al. Clin Interv Aging. 2016 May 17;11:665-81. doi: 10.2147/CIA.S105769. eCollection 2016. Clin Interv Aging. 2016. PMID: 27274215 Free PMC article. Review. - Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer's and Parkinson's diseases.
Corces MR, Shcherbina A, Kundu S, Gloudemans MJ, Frésard L, Granja JM, Louie BH, Eulalio T, Shams S, Bagdatli ST, Mumbach MR, Liu B, Montine KS, Greenleaf WJ, Kundaje A, Montgomery SB, Chang HY, Montine TJ. Corces MR, et al. Nat Genet. 2020 Nov;52(11):1158-1168. doi: 10.1038/s41588-020-00721-x. Epub 2020 Oct 26. Nat Genet. 2020. PMID: 33106633 Free PMC article. - Genome-wide significant, replicated and functional risk variants for Alzheimer's disease.
Guo X, Qiu W, Garcia-Milian R, Lin X, Zhang Y, Cao Y, Tan Y, Wang Z, Shi J, Wang J, Liu D, Song L, Xu Y, Wang X, Liu N, Sun T, Zheng J, Luo J, Zhang H, Xu J, Kang L, Ma C, Wang K, Luo X. Guo X, et al. J Neural Transm (Vienna). 2017 Nov;124(11):1455-1471. doi: 10.1007/s00702-017-1773-0. Epub 2017 Aug 2. J Neural Transm (Vienna). 2017. PMID: 28770390 Free PMC article. Review. - Genetic knowledge and attitudes towards genetic testing among final-year medical students at a public university in Ecuador.
Jaramillo-Aguilar DS, Simbaña-Rivera K. Jaramillo-Aguilar DS, et al. Front Med (Lausanne). 2024 Jun 19;11:1363552. doi: 10.3389/fmed.2024.1363552. eCollection 2024. Front Med (Lausanne). 2024. PMID: 38962733 Free PMC article. - Stem Cells as Potential Targets of Polyphenols in Multiple Sclerosis and Alzheimer's Disease.
Tandon A, Singh SJ, Chaturvedi RK. Tandon A, et al. Biomed Res Int. 2018 Jul 12;2018:1483791. doi: 10.1155/2018/1483791. eCollection 2018. Biomed Res Int. 2018. PMID: 30112360 Free PMC article. Review.
References
- Sturm R.A., Larsson M. Genetics of human iris colour and patterns. Pigment cell & melanoma research. 2009;22:544–562. - PubMed
- Liu F., van Duijn K., Vingerling J.R., Hofman A., Uitterlinden A.G., Janssens A.C., Kayser M. Eye color and the prediction of complex phenotypes from genotypes. Curr. Biol. 2009;19:R192–R193. - PubMed
- Sulem P., Gudbjartsson D.F., Stacey S.N., Helgason A., Rafnar T., Magnusson K.P., Manolescu A., Karason A., Palsson A., Thorleifsson G. Genetic determinants of hair, eye and skin pigmentation in Europeans. Nat. Genet. 2007;39:1443–1452. - PubMed
- Walsh S., Liu F., Ballantyne K.N., van Oven M., Lao O., Kayser M. IrisPlex: A sensitive DNA tool for accurate prediction of blue and brown eye colour in the absence of ancestry information. Forensic Sci Int Genet. 2010;5:170–180. - PubMed
Publication types
MeSH terms
Grants and funding
- R01 AA007535/AA/NIAAA NIH HHS/United States
- R01 AA014041/AA/NIAAA NIH HHS/United States
- R01 MH066206/MH/NIMH NIH HHS/United States
- AA13320/AA/NIAAA NIH HHS/United States
- R01 AA013321/AA/NIAAA NIH HHS/United States
- AA14041/AA/NIAAA NIH HHS/United States
- AA13326/AA/NIAAA NIH HHS/United States
- R01 AA013320/AA/NIAAA NIH HHS/United States
- AA13321/AA/NIAAA NIH HHS/United States
- AA10248/AA/NIAAA NIH HHS/United States
- R01 AA013326/AA/NIAAA NIH HHS/United States
- MH66206/MH/NIMH NIH HHS/United States
LinkOut - more resources
Full Text Sources
Molecular Biology Databases