Singaraja Roshni R, Brunham Liam R, Visscher Henk, Kastelein John J P, Hayden Michael R
Centre for Molecular Medicine and Therapeutics, University of British Columbia, and Children's and Women's Hospital , Vancouver, BC, Canada.
Arterioscler Thromb Vasc Biol. 2003 Aug 1;23(8):1322-32. doi: 10.1161/01.ATV.0000078520.89539.77. Epub 2003 May 22.
Approximately 50 mutations and many single nucleotide polymorphisms have been described in the ABCA1 gene, with mutations leading to Tangier disease and familial hypoalphalipoproteinemia. Homozygotes and heterozygotes for mutations in ABCA1 display a wide range of phenotypes. Identification of ABCA1 as the molecular defect in these diseases has allowed for ascertainment based on genetic status and determination of genotype-phenotype correlations and has permitted us to identify mutations conferring a range of severity of cellular, biochemical, and clinical phenotypes. In this study we review how genetic variation at the ABCA1 locus affects its role in the maintenance of lipid homeostasis and the natural progression of atherosclerosis.
ABCA1基因中已发现约50种突变和许多单核苷酸多态性,这些突变会导致Tangier病和家族性低α脂蛋白血症。ABCA1基因突变的纯合子和杂合子表现出广泛的表型。将ABCA1鉴定为这些疾病的分子缺陷,使得能够基于遗传状态进行确诊,并确定基因型与表型的相关性,还让我们能够识别出导致细胞、生化和临床表型严重程度各异的突变。在本研究中,我们回顾了ABCA1基因座的遗传变异如何影响其在维持脂质稳态和动脉粥样硬化自然进程中的作用。