Emergence of Novel Color Vision in Mice Engineered to Express a Human Cone Photopigment

Author:

Jacobs Gerald H.12345,Williams Gary A.12345,Cahill Hugh12345,Nathans Jeremy12345

Affiliation:

1. Neuroscience Research Institute and Department of Psychology, University of California, Santa Barbara, CA 93106, USA.

2. Department of Neuroscience, Johns Hopkins Medical School, Baltimore, MD 21205, USA.

3. Department of Ophthalmology, Johns Hopkins Medical School, Baltimore, MD 21205, USA.

4. Howard Hughes Medical Institute, Johns Hopkins Medical School, Baltimore, MD 21205, USA.

5. Department of Molecular Biology and Genetics, Johns Hopkins Medical School, Baltimore, MD 21205, USA.

Abstract

Changes in the genes encoding sensory receptor proteins are an essential step in the evolution of new sensory capacities. In primates, trichromatic color vision evolved after changes in X chromosome–linked photopigment genes. To model this process, we studied knock-in mice that expressed a human long-wavelength–sensitive (L) cone photopigment in the form of an X-linked polymorphism. Behavioral tests demonstrated that heterozygous females, whose retinas contained both native mouse pigments and human L pigment, showed enhanced long-wavelength sensitivity and acquired a new capacity for chromatic discrimination. An inherent plasticity in the mammalian visual system thus permits the emergence of a new dimension of sensory experience based solely on gene-driven changes in receptor organization.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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