Musarella M A
Long Island College Hospital, Department of Ophthalmology, Brooklyn, NY 11231, USA.
Doc Ophthalmol. 2001 May;102(3):165-77. doi: 10.1023/a:1017510515893.
Macular degeneration is a leading cause of blindness that affects the aged population. The complexity of the molecular basis of macular disease is now beginning to be elucidated with the identification of disease-causing genes. For example, mutations in the ABCR gene, (recently identified in cones as well) which codes for retinal rod-specific ABCR protein is responsible for Stargardt macular dystrophy/fundus flavimaculatus, an autosomal recessive macular dystrophy with juvenile onset, which accounts for 7% of human retinal degenerative diseases. The gene mutant in X-linked juvenile retinoschisis, XLRS1, is the first macular dystrophy gene to be isolated by positional cloning. Mutations in the peripherin/RDS gene have been shown to be associated with a variety of distinct forms of macular degenerations. The tissue inhibitor of metalloproteinase 3 (TIMP3) is implicated in autosomal dominant Sorsby fundus dystrophy. Best vitelliform macular dystrophy was mapped to 11q12-q13. The cloned gene product is the protein bestrophin, which is a retinal specific gene expressed in the RPE and possibly involved in the metabolism and transport of polyunsaturated fatty acids. The cloning of genes for rare heritable forms of macular degeneration will increase our understanding of the basic pathogenesis of the disease process. In the future this should also allow us to test the hypothesis that the coincidence of subclinical mutations in a number of genes involved in the formation and function of the macula can be responsible for cases of age-related macula-degeneration which is by far the most common form of these macular disorders.
黄斑变性是导致老年人失明的主要原因。随着致病基因的鉴定,黄斑疾病分子基础的复杂性现在开始得到阐明。例如,ABCR基因(最近在视锥细胞中也被发现)发生突变,该基因编码视网膜杆特异性ABCR蛋白,是导致Stargardt黄斑营养不良/眼底黄色斑点症的原因,这是一种常染色体隐性遗传性黄斑营养不良,发病于青少年时期,占人类视网膜退行性疾病的7%。X连锁青少年视网膜劈裂症的基因突变体XLRS1是第一个通过定位克隆分离出来的黄斑营养不良基因。外周蛋白/RDS基因的突变已被证明与多种不同形式的黄斑变性有关。金属蛋白酶3组织抑制剂(TIMP3)与常染色体显性遗传性Sorsby眼底营养不良有关。Best卵黄样黄斑营养不良被定位到11q12 - q13。克隆的基因产物是Bestrophin蛋白,它是一种在视网膜色素上皮(RPE)中表达的视网膜特异性基因,可能参与多不饱和脂肪酸的代谢和运输。克隆罕见遗传性黄斑变性的基因将增进我们对该疾病发病基本机制的理解。未来,这也将使我们能够检验这样一种假设,即参与黄斑形成和功能的多个基因发生亚临床突变的巧合可能是年龄相关性黄斑变性病例的病因,而年龄相关性黄斑变性是这些黄斑疾病中最常见的形式。