Giménez E, Giraldo P, Jeffery G, Montoliu L
Department of Molecular and Cellular Biology, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Genesis. 2001 May;30(1):21-5. doi: 10.1002/gene.1028.
Deletion of the tyrosinase locus control region (LCR) in transgenic mice results in variegated expression in the skin. Here we investigate the pigmentation pattern of other tissues that express tyrosinase: iris, choroid, and retina in the same animals. A mosaic distribution of pigmentation appears in the iris and choroid. Interestingly, a markedly different mosaic pattern is found in the retina, where central areas contain little or no melanin while pigmentation rises to normal levels towards periphery. Further, there is a temporal delay in the initiation and accumulation of pigment in retinal pigmented epithelium (RPE) cells during development, and patterns of adult retinal melanisation in these mice appear arrested at a stage found in early embryogenesis in wild-type mice. These results demonstrate that the tyrosinase LCR is needed for the correct establishment and maintenance of this expression domain throughout development, but particularly during the later stages of retinal melanisation.
在转基因小鼠中删除酪氨酸酶基因座控制区(LCR)会导致皮肤出现斑驳的表达。在此,我们研究了同一动物中表达酪氨酸酶的其他组织的色素沉着模式:虹膜、脉络膜和视网膜。色素沉着在虹膜和脉络膜中呈现镶嵌分布。有趣的是,在视网膜中发现了明显不同的镶嵌模式,其中中央区域几乎没有或没有黑色素,而色素沉着朝着周边上升至正常水平。此外,在发育过程中,视网膜色素上皮(RPE)细胞中色素的起始和积累存在时间延迟,并且这些小鼠成年视网膜黑化模式似乎停滞在野生型小鼠早期胚胎发育阶段所发现的一个阶段。这些结果表明,酪氨酸酶LCR对于在整个发育过程中,特别是在视网膜黑化的后期阶段,正确建立和维持这个表达域是必需的。