Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Proc Natl Acad Sci U S A. 2009 Dec 8;106(49):20948-53. doi: 10.1073/pnas.0910128106. Epub 2009 Nov 23.
Missense mutations in the cone opsins have been identified as a relatively common cause of red/green color vision defects, with the most frequent mutation being the substitution of arginine for cysteine at position 203 (C203R). When the corresponding cysteine is mutated in rhodopsin, it disrupts proper folding of the pigment, causing severe, early onset retinitis pigmentosa. While the C203R mutation has been associated with loss of cone function in color vision deficiency, it is not known what happens to cones expressing this mutant opsin. Here, we used high-resolution retinal imaging to examine the cone mosaic in two individuals with genes encoding a middle-wavelength sensitive (M) pigment with the C203R mutation. We found a significant reduction in cone density compared to normal and color-deficient controls, accompanying disruption in the cone mosaic in both individuals, and thinning of the outer nuclear layer. The C203R mosaics were different from that produced by another mutation (LIAVA) previously shown to disrupt the cone mosaic. Comparison of these mosaics provides insight into the timing and degree of cone disruption and has implications for the prospects for restoration of vision loss associated with various cone opsin mutations.
已经确定,视锥蛋白中的错义突变是导致红/绿色觉缺陷的一个相对常见的原因,最常见的突变是将精氨酸替换为 203 位的半胱氨酸(C203R)。当视蛋白中的相应半胱氨酸发生突变时,会破坏色素的正确折叠,导致严重的、早发性视网膜色素变性。虽然 C203R 突变与色觉缺陷中的视锥功能丧失有关,但尚不清楚表达这种突变视蛋白的视锥会发生什么。在这里,我们使用高分辨率视网膜成像技术检查了两个携带编码中波敏感(M)色素的基因发生 C203R 突变的个体的视锥马赛克。我们发现与正常和色觉缺陷对照相比,视锥密度显著降低,两个个体的视锥马赛克都受到破坏,外核层变薄。C203R 马赛克与先前显示破坏视锥马赛克的另一种突变(LIAVA)产生的马赛克不同。对这些马赛克的比较提供了对视锥破坏的时间和程度的深入了解,对各种视锥蛋白突变相关的视力丧失恢复的前景具有重要意义。