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
相关论文
共 45 条
[11]  
Gardner JC, 2009, MOL VIS, V15, P876
[12]  
Georges P, 1999, J COMP NEUROL, V413, P198
[13]  
GOTTLOB I, 1994, INVEST OPHTH VIS SCI, V35, P3556
[14]   Defective development of photoreceptor membranes in a mouse model of recessive retinal degeneration [J].
Gross, Alecia K. ;
Decker, Glenn ;
Chan, Fung ;
Sandoval, Ivette M. ;
Wilson, John H. ;
Wensel, Theodore G. .
VISION RESEARCH, 2006, 46 (27) :4510-4518
[15]   Improvement in retinal image quality with dynamic correction of the eye's aberrations [J].
Hofer, H ;
Chen, L ;
Yoon, GY ;
Singer, B ;
Yamauchi, Y ;
Williams, DR .
OPTICS EXPRESS, 2001, 8 (11) :631-643
[16]   Retinopathy induced in mice by targeted disruption of the rhodopsin gene [J].
Humphries, MM ;
Rancourt, D ;
Farrar, GJ ;
Kenna, P ;
Hazel, M ;
Bush, RA ;
Sieving, PA ;
Sheils, DM ;
McNally, N ;
Creighton, P ;
Erven, A ;
Boros, A ;
Gulya, K ;
Capecchi, MR ;
Humphries, P .
NATURE GENETICS, 1997, 15 (02) :216-219
[17]   Blue cone monochromatism: clinical findings in patients with mutations in the red/green opsin gene cluster [J].
Kellner, U ;
Wissinger, B ;
Tippmann, S ;
Kohl, S ;
Kraus, H ;
Foerster, MH .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2004, 242 (09) :729-735
[18]   A new mechanism in blue cone monochromatism [J].
LadekjaerMikkelsen, AS ;
Rosenberg, T ;
Jorgensen, AL .
HUMAN GENETICS, 1996, 98 (04) :403-408
[19]   Wild-Type Cone Photoreceptors Persist Despite Neighboring Mutant Cone Degeneration [J].
Lewis, Alaron ;
Williams, Philip ;
Lawrence, Owen ;
Wong, Rachel O. L. ;
Brockerhoff, Susan E. .
JOURNAL OF NEUROSCIENCE, 2010, 30 (01) :382-389
[20]   Automated identification of cone photoreceptors in adaptive optics retinal images [J].
Li, Kaccie Y. ;
Roorda, Austin .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 2007, 24 (05) :1358-1363