Deletion of the X-linked opsin gene array locus control region (LCR) results in disruption of the cone mosaic

被引:44
作者
Carroll, Joseph [1 ,2 ,3 ]
Rossi, Ethan A. [4 ]
Porter, Jason [5 ]
Neitz, Jay [6 ]
Roorda, Austin [4 ]
Williams, David R. [7 ]
Neitz, Maureen [6 ]
机构
[1] Med Coll Wisconsin, Dept Ophthalmol, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Cell Biol Neurobiol & Anat, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Dept Biophys, Milwaukee, WI 53226 USA
[4] Univ Calif Berkeley, Sch Optometry, Berkeley, CA 94720 USA
[5] Univ Houston, Coll Optometry, Houston, TX 77204 USA
[6] Univ Washington, Dept Ophthalmol, Seattle, WA 98195 USA
[7] Univ Rochester, Ctr Visual Sci, Rochester, NY 14627 USA
关键词
Adaptive optics; Blue cone monochromacy; Color vision; Cones; Opsin; Photopigment; MUTUALLY EXCLUSIVE EXPRESSION; ADAPTIVE OPTICS; COLOR-VISION; PIGMENT GENES; HUMAN RED; MONOCHROMATISM; PHOTORECEPTORS; RETINA; DEGENERATION; MUTATIONS;
D O I
10.1016/j.visres.2010.07.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Blue cone monochromacy (BCM) is an X-linked condition in which long- (L) and middle- (M) wavelength-sensitive cone function is absent. Due to the X-linked nature of the condition, female carriers are spared from a full manifestation of the associated defects but can show visual symptoms, including abnormal cone electroretinograms. Here we imaged the cone mosaic in four females carrying an L/M array with deletion of the locus control region, resulting in an absence of L/M opsin gene expression (effectively acting as a cone opsin knockout). On average, they had cone mosaics with reduced density and disrupted organization compared to normal trichromats. This suggests that the absence of opsin in a subset of cones results in their early degeneration, with X-inactivation the likely mechanism underlying phenotypic variability in BCM carriers. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1989 / 1999
页数:11
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