Document Detail


Trichromatic color vision with only two spectrally distinct photopigments.
MedLine Citation:
PMID:  10491608     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
J Neitz; M Neitz; J C He; S K Shevell
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Nature neuroscience     Volume:  2     ISSN:  1097-6256     ISO Abbreviation:  Nat. Neurosci.     Publication Date:  1999 Oct 
Date Detail:
Created Date:  1999-11-19     Completed Date:  1999-11-19     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9809671     Medline TA:  Nat Neurosci     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  884-8     Citation Subset:  IM    
Affiliation:
Department of Cell Biology, Neurobiology & Anatomy and Department of Ophthalmology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, Wisconsin 53226-4812, USA. jneitz@mcw.edu
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MeSH Terms
Descriptor/Qualifier:
Amino Acid Substitution
Color Vision Defects / genetics*
Discrimination (Psychology) / physiology*
Humans
Linkage (Genetics)*
Retinal Pigments / physiology*
X Chromosome*
Chemical
Reg. No./Substance:
0/Retinal Pigments

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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