Discovery and Functional Annotation of SIX6 Variants in Primary Open-Angle Glaucoma

Megan Ulmer Carnes, Yangfan P. Liu, R. Rand Allingham, Benjamin T. Whigham, Shane Havens, Melanie E. Garrett, Chunyan Qiao, Elias Nicholas Katsanis, Janey L. Wiggs, Louis R. Pasquale, Allison Ashley-Koch, Edwin C. Oh, Michael A. Hauser, Murray Brilliant, Donald L. Budenz, Hemin R. Chin, Jessica Cooke Bailey, John Fingert, David S. Friedman, Douglas GaasterlandTerry Gaasterland, Jonathan Haines, Michael A. Hauser, Jae H. Kang, Richard K. Lee, Paul R. Lichter, Yutao Liu, Stephanie Loomis, Cathy Essentia McCarty, Sayoko E. Moroi, Louis R. Pasquale, Margaret Pericak-Vance, Anthony Realini, Julia E. Richards, Joel S. Schuman, William K. Scott, Kuldev Singh, Arthur Sit, Douglas Vollrath, Robert N. Weinreb, Janey L. Wiggs, Gadi Wollstein, Brian L. Yaspan, Don Zack, Kang Zhang

Research output: Contribution to journalArticlepeer-review

78 Scopus citations


Glaucoma is a leading cause of blindness worldwide. Primary open-angle glaucoma (POAG) is the most common subtype and is a complex trait with multigenic inheritance. Genome-wide association studies have previously identified a significant association between POAG and the SIX6 locus (rs10483727, odds ratio (OR) = 1.32, p = 3.87×10-11). SIX6 plays a role in ocular development and has been associated with the morphology of the optic nerve. We sequenced the SIX6 coding and regulatory regions in 262 POAG cases and 256 controls and identified six nonsynonymous coding variants, including five rare and one common variant, Asn141His (rs33912345), which was associated significantly with POAG (OR = 1.27, p = 4.2×10-10) in the NEIGHBOR/GLAUGEN datasets. These variants were tested in an in vivo Danio rerio (zebrafish) complementation assay to evaluate ocular metrics such as eye size and optic nerve structure. Five variants, found primarily in POAG cases, were hypomorphic or null, while the sixth variant, found only in controls, was benign. One variant in the SIX6 enhancer increased expression of SIX6 and disrupted its regulation. Finally, to our knowledge for the first time, we have identified a clinical feature in POAG patients that appears to be dependent upon SIX6 genotype: patients who are homozygous for the SIX6 risk allele (His141) have a statistically thinner retinal nerve fiber layer than patients homozygous for the SIX6 non-risk allele (Asn141). Our results, in combination with previous SIX6 work, lead us to hypothesize that SIX6 risk variants disrupt the development of the neural retina, leading to a reduced number of retinal ganglion cells, thereby increasing the risk of glaucoma-associated vision loss.

Original languageEnglish (US)
Article numbere1004372
JournalPLoS genetics
Issue number5
StatePublished - May 1 2014

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics
  • Ecology, Evolution, Behavior and Systematics
  • Molecular Biology
  • Cancer Research


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