Mehrabian M, Wong J, Wang X, Jiang Z, Shi W, Fogelman A M, Lusis A J
Department of Medicine, University of California, Los Angeles, USA.
Circ Res. 2001 Jul 20;89(2):125-30. doi: 10.1161/hh1401.093458.
The genes contributing to the common forms of atherosclerosis are largely unknown. One approach to dissecting complex traits such as atherosclerosis is to use animal models, such as the mouse, to map and characterize the genetic loci involved. We now report the identification of a locus for aortic lesion formation on mouse chromosome 6 that exhibits a highly significant lod score of 6.7 in a genetic cross between the susceptible strain, C57BL/6J, and the resistant strain, CAST/Ei. The locus was confirmed by constructing a congenic strain in which the chromosome 6 segment from CAST/Ei was transferred to a C57BL/6J background in a series of backcrosses. The congenic strain was almost completely resistant to diet-induced atherosclerosis. The chromosome 6 segment was also transferred onto the background of an LDL receptor-null mutation and resulted again in almost complete resistance to aortic lesion formation. This locus also influenced insulin levels but did not affect plasma lipoprotein levels, blood pressure, or body fat. The chromosome 6 gene, which we call Artles (for arterial lesions), did not affect endothelial cell responses to oxidized LDL, but lesion formation was partially reduced through bone marrow transplantation. The locus contains the candidate gene peroxisome proliferator-activated receptor-gamma, and the congenic mice exhibited significantly reduced expression of peroxisome proliferator-activated receptor-gamma.
导致常见形式动脉粥样硬化的基因在很大程度上尚不清楚。剖析诸如动脉粥样硬化这类复杂性状的一种方法是使用动物模型,如小鼠,来定位和表征相关的基因位点。我们现在报告在小鼠6号染色体上鉴定出一个主动脉病变形成的位点,在易感品系C57BL/6J和抗性品系CAST/Ei之间的遗传杂交中,该位点显示出高达6.7的高度显著的lod值。通过构建一个同类系来确认该位点,在一系列回交中,将CAST/Ei的6号染色体片段转移到C57BL/6J背景中。该同类系对饮食诱导的动脉粥样硬化几乎完全具有抗性。6号染色体片段也被转移到低密度脂蛋白受体缺失突变的背景上,再次导致对主动脉病变形成几乎完全具有抗性。这个位点也影响胰岛素水平,但不影响血浆脂蛋白水平、血压或体脂。我们称为Artles(动脉病变之意)的6号染色体基因不影响内皮细胞对氧化低密度脂蛋白的反应,但通过骨髓移植,病变形成部分减少。该位点包含候选基因过氧化物酶体增殖物激活受体γ,并且同类系小鼠过氧化物酶体增殖物激活受体γ的表达显著降低。