A photic visual cycle of rhodopsin regeneration is dependent on Rgr

被引:154
作者
Chen, P
Hao, WS
Rife, L
Wang, XP
Shen, DW
Chen, J
Ogden, T
Van Boemel, GB
Wu, LY
Yang, M
Fong, HKW [1 ]
机构
[1] Univ So Calif, Keck Sch Med, Dept Ophthalmol, Los Angeles, CA 90033 USA
[2] Univ So Calif, Keck Sch Med, Dept Microbiol, Los Angeles, CA 90033 USA
[3] Univ So Calif, Keck Sch Med, Dept Cell & Neurobiol, Los Angeles, CA 90033 USA
[4] Univ So Calif, Keck Sch Med, Norris Canc Ctr, Los Angeles, CA 90033 USA
[5] Univ So Calif, Sch Dent, Ctr Craniofacial Mol Biol, Los Angeles, CA 90033 USA
[6] Doheny Eye Inst, Los Angeles, CA 90033 USA
关键词
D O I
10.1038/90089
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
During visual excitation, rhodopsin undergoes photoactivation and bleaches to opsin and all-trans-retinal(1,2). To regenerate rhodopsin and maintain normal visual sensitivity, the all-trans isomer must be metabolized and reisomerized to produce the chromophore 11-cis-retinal in biochemical steps that constitute the visual cycle and involve the retinal pigment epithelium (RPE; refs, 3-8). A key step in the visual cycle is isomerization of an all-trans retinoid to 11-cis-retinol in the RPE (refs, 9-11). It could be that the retinochrome-like opsins. peropsin, or the retinal G protein-coupled receptor (RGR) opsin12-16 are isomerases in the RPE. In contrast to visual pigments. RGR is bound predominantly to endogenous all-transretinal, and irradiation of RGR in vitro results in stereospecific conversion of the bound all-trans isomer to 11-cis-retinal(17). Here we show that RGR is involved in the formation of 11-cis-retinal in mice and functions in a light-dependent pathway of the rod visual cycle. Mutations in the human gene encoding RGR are associated with retinitis pigmentosa(18).
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页码:256 / 260
页数:5
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