Topographical cone photopigment in deutan-type red-green color gene expression vision defects

被引:9
|
作者
Bollinger, K
Sjoberg, SA
Neitz, M
Neitz, J
机构
[1] Med Coll Wisconsin, Dept Cellular Biol Neurobiol & Anat, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Ophthalmol, Milwaukee, WI 53226 USA
关键词
color blindness; gene expression; photopigment genes; deuteranomaly; topography;
D O I
10.1016/j.visres.2003.09.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Eye donors were identified who had X-chromosome photopigment gene arrays like those of living deuteranomalous men; the arrays contained two genes encoding long-wavelength sensitive (L) pigments as well as genes to encode middle-wavelength sensitive (M) photopigment. Ultrasensitive methods failed to detect the presence of M photopigment mRNA in the retinas of these deutan donors. This provides direct evidence that deuteranomaly is caused by the complete absence of M pigment mRNA. Additionally, for those eyes with mRNA corresponding to two different L-type photopigments, the ratio of mRNA from the first vs. downstream L genes was analyzed across the retinal topography. Results show that the pattern of first relative to downstream L gene expression in the deuteranomalous retina is similar to the pattern of L vs. M gene expression found in normal retinas. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:135 / 145
页数:11
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