The importance of deleterious mutations of M pigment genes as a cause of color vision defects

Kathryn Bollinger, Carolyn Bialozynski, Jay Neitz, Maureen Neitz

Research output: Contribution to journalArticle

11 Scopus citations

Abstract

Numbers and ratios of pigment genes were estimated in a sample of young males with color-vision deficiencies. Eighteen were estimated to have a single L pigment gene on the X-chromosome. In most cases, the one L gene was the only X-linked photopigment gene, as has been reported previously for deuteranopes. However, four of the boys in this group were estimated to have M pigment genes in addition to a single L. Sequences of exons 2-4 of the M genes were obtained from two of the subjects whose ratios indicated one L and two M genes. A substitution of cytosine for thymine was found at nucleotide position 1101 (numbering system from Nathans1) of both M genes of both males. This mutation interrupts the function of the encoded M photopigments by replacing cysteine with arginine at amino acid position 203. Deuteranopia is often caused by the loss of M genes, but here we report that it can also be caused by inissense mutations that interrupt the function of all M pigments. In these cases, all photoreceptors that would normally be M cones presumably express the defective opsin. With all the M cones disabled, the total number of functional cones would be fewer than normal in these deuteranopic eyes. & 2000 John Wiley & Sons, Inc.

Original languageEnglish (US)
JournalColor Research and Application
Volume26
Issue numberSUPPL.
Publication statusPublished - Dec 1 2001
Externally publishedYes

    Fingerprint

Keywords

  • Blue cone monochromat
  • Color vision
  • Color vision deficiency
  • Cone photoreceptors
  • Deuteranopia
  • Genetics
  • Photopigments

ASJC Scopus subject areas

  • Human Factors and Ergonomics
  • Chemistry(all)
  • Chemical Engineering(all)

Cite this