Literature DB >> 10491608

Trichromatic color vision with only two spectrally distinct photopigments.

J Neitz1, M Neitz, J C He, S K Shevell.   

Abstract

Protanomaly is a common, X-linked abnormality of color vision. Like people with normal color vision, protanomalous observers are trichromatic, but their ability to discriminate colors in the red-green part of the spectrum is reduced because the photopigments that mediate discrimination in this range are abnormally similar. Whereas normal subjects have pigments whose wavelengths of peak sensitivity differ by about 30 nm, the peak wavelengths for protanomalous observers are thought to differ by only a few nanometers. We found, however, that although this difference occurred in some protanomalous subjects, others had pigments whose peak wavelengths were identical. Genetic and psychophysical results from the latter class indicated that limited red-green discrimination can be achieved with pigments that have the same peak wavelength sensitivity and that differ only in optical density. A single amino acid substitution was correlated with trichromacy in these subjects, suggesting that differences in pigment sequence may regulate the optical density of the cone.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10491608     DOI: 10.1038/13185

Source DB:  PubMed          Journal:  Nat Neurosci        ISSN: 1097-6256            Impact factor:   24.884


  14 in total

1.  Photopigment optical density of the human foveola and a paradoxical senescent increase outside the fovea.

Authors:  Agnes B Renner; Holger Knau; Maureen Neitz; Jay Neitz; John S Werner
Journal:  Vis Neurosci       Date:  2004 Nov-Dec       Impact factor: 3.241

Review 2.  The genetics of normal and defective color vision.

Authors:  Jay Neitz; Maureen Neitz
Journal:  Vision Res       Date:  2010-12-15       Impact factor: 1.886

3.  Simulations of adaptation and color appearance in observers with varying spectral sensitivity.

Authors:  Michael A Webster; Igor Juricevic; Kyle C McDermott
Journal:  Ophthalmic Physiol Opt       Date:  2010-09       Impact factor: 3.117

4.  Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscope.

Authors:  Maureen Neitz; Joseph Carroll; Agnes Renner; Holger Knau; John S Werner; Jay Neitz
Journal:  Vis Neurosci       Date:  2004 May-Jun       Impact factor: 3.241

5.  Signatures of selection and gene conversion associated with human color vision variation.

Authors:  Brian C Verrelli; Sarah A Tishkoff
Journal:  Am J Hum Genet       Date:  2004-07-13       Impact factor: 11.025

6.  Cone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsin.

Authors:  Joseph Carroll; Rigmor C Baraas; Melissa Wagner-Schuman; Jungtae Rha; Cory A Siebe; Christina Sloan; Diane M Tait; Summer Thompson; Jessica I W Morgan; Jay Neitz; David R Williams; David H Foster; Maureen Neitz
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-23       Impact factor: 11.205

7.  A study of unusual Rayleigh matches in deutan deficiency.

Authors:  J L Barbur; M Rodriguez-Carmona; J A Harlow; K Mancuso; J Neitz; M Neitz
Journal:  Vis Neurosci       Date:  2008 May-Jun       Impact factor: 3.241

8.  Photopigment genes, cones, and color update: disrupting the splicing code causes a diverse array of vision disorders.

Authors:  Maureen Neitz; Sara S Patterson; Jay Neitz
Journal:  Curr Opin Behav Sci       Date:  2019-07-19

9.  Neurobiological hypothesis of color appearance and hue perception.

Authors:  Brian P Schmidt; Maureen Neitz; Jay Neitz
Journal:  J Opt Soc Am A Opt Image Sci Vis       Date:  2014-04-01       Impact factor: 2.129

10.  Genetic Testing as a New Standard for Clinical Diagnosis of Color Vision Deficiencies.

Authors:  Candice Davidoff; Maureen Neitz; Jay Neitz
Journal:  Transl Vis Sci Technol       Date:  2016-09-06       Impact factor: 3.283

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.