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患有斯塔加特病和年龄相关性黄斑变性的家族中突变ABCR(ABCA4)等位基因的共分离及功能分析。

Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration.

作者信息

Shroyer N F, Lewis R A, Yatsenko A N, Wensel T G, Lupski J R

机构信息

Program in Cell and Molecular Biology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Hum Mol Genet. 2001 Nov 1;10(23):2671-8. doi: 10.1093/hmg/10.23.2671.

Abstract

Mutations in ABCR (ABCA4) have been reported to cause a spectrum of autosomal recessively inherited retinopathies, including Stargardt disease (STGD), cone-rod dystrophy and retinitis pigmentosa. Individuals heterozygous for ABCR mutations may be predisposed to develop the multifactorial disorder age-related macular degeneration (AMD). We hypothesized that some carriers of STGD alleles have an increased risk to develop AMD. We tested this hypothesis in a cohort of families that manifest both STGD and AMD. With a direct-sequencing mutation detection strategy, we found that AMD-affected relatives of STGD patients are more likely to be carriers of pathogenic STGD alleles than predicted based on chance alone. We further investigated the role of AMD-associated ABCR mutations by testing for expression and ATP-binding defects in an in vitro biochemical assay. We found that mutations associated with AMD have a range of assayable defects ranging from no detectable defect to apparent null alleles. Of the 21 missense ABCR mutations reported in patients with AMD, 16 (76%) show abnormalities in protein expression, ATP-binding or ATPase activity. We infer that carrier relatives of STGD patients are predisposed to develop AMD.

摘要

据报道,ABCR(ABCA4)基因突变会导致一系列常染色体隐性遗传视网膜病变,包括斯特格氏病(STGD)、锥杆营养不良和色素性视网膜炎。ABCR基因突变的杂合个体可能易患多因素疾病年龄相关性黄斑变性(AMD)。我们推测,一些STGD等位基因携带者患AMD的风险增加。我们在一组同时患有STGD和AMD的家族中验证了这一假设。通过直接测序突变检测策略,我们发现,与仅基于概率预测的情况相比,STGD患者的AMD患病亲属更有可能是致病性STGD等位基因的携带者。我们通过体外生化试验检测表达和ATP结合缺陷,进一步研究了与AMD相关的ABCR突变的作用。我们发现,与AMD相关的突变存在一系列可检测到的缺陷,从无可检测到的缺陷到明显的无效等位基因。在AMD患者中报告的21种错义ABCR突变中,16种(76%)在蛋白质表达、ATP结合或ATP酶活性方面表现异常。我们推断,STGD患者的携带等位基因亲属易患AMD。

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