Molday Robert S, Zhong Ming, Quazi Faraz
Department of Biochemistry, Centre for Macular Research, University of British Columbia, Vancouver, B.C., Canada V6T 1Z3.
Biochim Biophys Acta. 2009 Jul;1791(7):573-83. doi: 10.1016/j.bbalip.2009.02.004. Epub 2009 Feb 20.
ABCA4 is a member of the ABCA subfamily of ATP binding cassette (ABC) transporters that is expressed in rod and cone photoreceptors of the vertebrate retina. ABCA4, also known as the Rim protein and ABCR, is a large 2,273 amino acid glycoprotein organized as two tandem halves, each containing a single membrane spanning segment followed sequentially by a large exocytoplasmic domain, a multispanning membrane domain and a nucleotide binding domain. Over 500 mutations in the gene encoding ABCA4 are associated with a spectrum of related autosomal recessive retinal degenerative diseases including Stargardt macular degeneration, cone-rod dystrophy and a subset of retinitis pigmentosa. Biochemical studies on the purified ABCA4 together with analysis of abca4 knockout mice and patients with Stargardt disease have implicated ABCA4 as a retinylidene-phosphatidylethanolamine transporter that facilitates the removal of potentially reactive retinal derivatives from photoreceptors following photoexcitation. Knowledge of the genetic and molecular basis for ABCA4 related retinal degenerative diseases is being used to develop rationale therapeutic treatments for this set of disorders.
ABCA4是ATP结合盒(ABC)转运蛋白ABCA亚家族的成员,在脊椎动物视网膜的视杆和视锥光感受器中表达。ABCA4也被称为边缘蛋白和ABCR,是一种由2273个氨基酸组成的大型糖蛋白,由两个串联的部分组成,每个部分都包含一个单一的跨膜片段,随后依次是一个大的胞外结构域、一个多跨膜结构域和一个核苷酸结合结构域。编码ABCA4的基因中有500多个突变与一系列相关的常染色体隐性视网膜退行性疾病有关,包括斯特格黄斑变性、视锥视杆营养不良和视网膜色素变性的一个子集。对纯化的ABCA4进行的生化研究,以及对abca4基因敲除小鼠和斯特格病患者的分析表明,ABCA4是一种视黄醛磷脂酰乙醇胺转运蛋白,它有助于在光激发后从光感受器中清除潜在的反应性视网膜衍生物。ABCA4相关视网膜退行性疾病的遗传和分子基础知识正被用于开发针对这组疾病的合理治疗方法。