Travis G H, Sutcliffe J G, Bok D
Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas 75235.
Neuron. 1991 Jan;6(1):61-70. doi: 10.1016/0896-6273(91)90122-g.
Mice homozygous for the retinal degeneration slow (rds) mutation exhibit abnormal development of photoreceptor cells, followed by their slow degeneration. We have recently cloned the rds gene and determined the structure of the wild-type rds mRNA. Here we show that the gene is expressed exclusively in photoreceptor cells. We demonstrate that it encodes a 39 kd membrane-associated glycoprotein that is restricted to photoreceptor outer segments. By electron microscopy, we show that the rds protein is distributed uniformly within outer segment discs. The developmental appearance of the rds protein coincides with outer segment disc formation. We propose that the rds protein functions as an adhesion molecule for stabilization of the outer segment discs.
视网膜变性缓慢(rds)突变的纯合子小鼠表现出光感受器细胞发育异常,随后逐渐缓慢退化。我们最近克隆了rds基因并确定了野生型rds mRNA的结构。在此我们表明该基因仅在光感受器细胞中表达。我们证明它编码一种39kd的膜相关糖蛋白,该蛋白局限于光感受器外段。通过电子显微镜,我们显示rds蛋白在外段盘膜内均匀分布。rds蛋白的发育出现与外段盘膜的形成相一致。我们提出rds蛋白作为一种黏附分子,用于稳定外段盘膜。