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Curr Opin Genet Dev. 2006 Jun;16(3):301-7. Epub 2006 May 2.

Genetics of variation in human color vision and the retinal cone mosaic.

Author information

1
Departments of Medicine, Medical Genetics and Genome Sciences, University of Washington, Seattle, WA 98185, USA. sdeeb@u.washington.edu

Abstract

Variation in human color vision is mainly caused by one common polymorphism (Ser180Ala) in the L pigment, and to the frequent presence of hybrid genes that encode pigments with various spectral properties. Both recombination and gene conversion between the highly homologous L and M pigment genes have generated wide variation in genotype and color vision phenotype. The S, M and L cones are distributed randomly in the central retina. Unlike S cones, M and L cones vary widely in number within the central retina. Determining the number of the three classes of cone and their special distribution in the living retina has significantly advanced the ability to correlate the cone mosaic in normal and color-defective subjects with the color vision phenotype. The transcription factors NR2E3, TRbeta2 and RXRgamma play crucial roles in establishment of the retinal cone mosaic during eye development.

PMID:
16647849
DOI:
10.1016/j.gde.2006.04.002
[Indexed for MEDLINE]

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