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本文引用的文献

1
ABCA4 disease progression and a proposed strategy for gene therapy.ABCA4疾病进展及一种基因治疗的提议策略。
Hum Mol Genet. 2009 Mar 1;18(5):931-41. doi: 10.1093/hmg/ddn421. Epub 2008 Dec 12.
2
Role of the C terminus of the photoreceptor ABCA4 transporter in protein folding, function, and retinal degenerative diseases.光感受器ABCA4转运蛋白C末端在蛋白质折叠、功能及视网膜退行性疾病中的作用
J Biol Chem. 2009 Feb 6;284(6):3640-9. doi: 10.1074/jbc.M806580200. Epub 2008 Dec 4.
3
Review. Structure and mechanism of ATP-binding cassette transporters.综述:ATP结合盒转运蛋白的结构与机制
Philos Trans R Soc Lond B Biol Sci. 2009 Jan 27;364(1514):239-45. doi: 10.1098/rstb.2008.0125.
4
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics.针对RPE65异构酶缺乏症的人类基因疗法可激活视觉的视黄醛循环,但视杆动力学缓慢。
Proc Natl Acad Sci U S A. 2008 Sep 30;105(39):15112-7. doi: 10.1073/pnas.0807027105. Epub 2008 Sep 22.
5
Retinopathy in mice induced by disrupted all-trans-retinal clearance.全反式视黄醛清除障碍诱导的小鼠视网膜病变
J Biol Chem. 2008 Sep 26;283(39):26684-93. doi: 10.1074/jbc.M804505200. Epub 2008 Jul 25.
6
Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapy.通过慢病毒基因疗法纠正斯塔加特病小鼠模型中的疾病表型。
Gene Ther. 2008 Oct;15(19):1311-20. doi: 10.1038/gt.2008.78. Epub 2008 May 8.
7
Effect of gene therapy on visual function in Leber's congenital amaurosis.基因治疗对莱伯先天性黑蒙视觉功能的影响。
N Engl J Med. 2008 May 22;358(21):2231-9. doi: 10.1056/NEJMoa0802268. Epub 2008 Apr 27.
8
Safety and efficacy of gene transfer for Leber's congenital amaurosis.基因转移治疗莱伯先天性黑蒙的安全性和有效性。
N Engl J Med. 2008 May 22;358(21):2240-8. doi: 10.1056/NEJMoa0802315. Epub 2008 Apr 27.
9
Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice.腺相关病毒载体中大型基因的血清型依赖性包装可实现对小鼠的有效基因递送。
J Clin Invest. 2008 May;118(5):1955-64. doi: 10.1172/JCI34316.
10
Recovery of rod photoresponses in ABCR-deficient mice.ABCR 缺陷小鼠视杆光反应的恢复
Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2743-55. doi: 10.1167/iovs.07-1499. Epub 2008 Feb 8.

光感受器ABC转运蛋白ABCA4在脂质转运及斯塔加特黄斑变性中的作用

The role of the photoreceptor ABC transporter ABCA4 in lipid transport and Stargardt macular degeneration.

作者信息

Molday Robert S, Zhong Ming, Quazi Faraz

机构信息

Department of Biochemistry, Centre for Macular Research, University of British Columbia, Vancouver, B.C., Canada V6T 1Z3.

出版信息

Biochim Biophys Acta. 2009 Jul;1791(7):573-83. doi: 10.1016/j.bbalip.2009.02.004. Epub 2009 Feb 20.

DOI:10.1016/j.bbalip.2009.02.004
PMID:19230850
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2746242/
Abstract

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.

摘要

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。