GENES AND VISUAL PIGMENTS OF RED-GREEN COLOR VISION

红绿色视觉的基因和视觉色素

• 批准号: 6635618
• 负责人: MAUREEN E NEITZ
• 金额: $ 33.64万
• 依托单位: MEDICAL COLLEGE OF WISCONSIN
• 依托单位国家: 美国
• 财政年份: 1991
• 资助国家: 美国
• 起止时间: 1991-08-01 至 2005-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6635618
• 关键词: clinical research; color blindness; color visions; cone cell; electroretinography; fluorescent in situ hybridization; gene expression; gene rearrangement; genetic carriers; genotype; human genetic material tag; human subject; male; molecular cloning; molecular genetics; nucleic acid sequence; nucleic acid structure; phenotype; point mutation; polymerase chain reaction; psychophysics; rhodopsin; sex linked trait; southern blotting; vision disorders; visual pigments

Most of our daily activities are performed at light levels where vision is based on cone photoreceptors. A feature of cone-based vision is the capacity to see in color. Color is an important component of the information that we gather with our eyes; we use color so automatically that we fail to appreciate how important it is. It serves as a non-linguistic code that gives us instant information about the world around us. Common inherited variations in color vision provide a unique system in which to study the effects of alterations in the cone mosaic on visual function and how a variation in the amino acid sequence of the cone opsin affects cone photoreceptor function. The long-term goals of the proposed research are to understand the molecular genetics of cone-based vision, and to understand the relationship between genotype and phenotype. A practical application of this work is the development of a genetic test to distinguish between inherited color vision deficiencies, and color vision loss acquired secondary to disease or exposure to toxic chemicals or drugs. The specific aims are: 1) To determine the distribution of variation in the L:M cone ratio in the color normal population and to determine the extent to which the L:M cone ratio is specified by the X-chromosome visual pigment gene locus. 2) To investigate the effects of naturally occurring differences in primary amino acid sequence of X-encoded cone pigments on function, specifically with regard to alterations in cone spectral sensitivity and optical density. 3) To investigate specific phenotype/genotype relationships underlying color vision deficiencies with regard to a) the role of deleterious mutations in cone pigments in vision disorders; b) the molecular basis for variation in the severity of protan color vision defects; and c) the molecular genetic basis for color vision loss in males with a very mild defect but with normal looking pigment gene arrays, and females carriers who exhibit color vision abnormalities. To achieve these goals we will take a multidisciplinary approach, using psychophysical, electrophysiological and molecular biological techniques.

我们的大多数日常活动都是在光水平下进行的，其中视觉是基于锥状光感受器的。视锥细胞视觉的一个特点是能够看到颜色。颜色是我们用眼睛收集的信息的重要组成部分;我们如此自动地使用颜色，以至于我们没有意识到它的重要性。它作为一种非语言代码，为我们提供关于我们周围世界的即时信息。常见的遗传性色觉变异提供了一个独特的系统，在其中研究改变视锥马赛克对视觉功能的影响，以及视锥视蛋白的氨基酸序列的变化如何影响视锥光感受器功能。该研究的长期目标是了解视锥细胞视觉的分子遗传学，并了解基因型和表型之间的关系。这项工作的一个实际应用是开发一种基因测试，以区分遗传性色觉缺陷和继发于疾病或暴露于有毒化学品或药物的色觉丧失。具体目标是：1）确定L：M视锥细胞比率在颜色正常人群中的变异分布，并确定L：M视锥细胞比率在多大程度上由X染色体视色素基因座指定。2)研究X编码锥色素一级氨基酸序列的天然差异对功能的影响，特别是锥光谱敏感性和光密度的改变。3)研究色觉缺陷的特定表型/基因型关系，涉及a）视锥色素中有害突变在视觉障碍中的作用; B）原色素色觉缺陷严重程度变化的分子基础;和c）在具有非常轻微缺陷但具有正常外观色素基因阵列的男性中色觉丧失的分子遗传基础，以及色觉异常的女性携带者。为了实现这些目标，我们将采取多学科的方法，使用心理物理学，电生理学和分子生物学技术。