Colinayo Veronica V, Qiao Jian-Hua, Wang Xuping, Krass Kelly L, Schadt Eric, Lusis Aldons J, Drake Thomas A
Department of Microbiology, Immunology and Molecular Genetics, University of California-Los Angeles, Los Angeles, California 90095, USA.
Mamm Genome. 2003 Jul;14(7):464-71. doi: 10.1007/s00335-002-2187-2.
Genetic factors independent of those affecting plasma lipid levels are a major contributor to risk for atherosclerosis in humans, yet the basis for these is poorly understood. This study examined plasma lipids and diet-induced atherosclerosis in 16-month-old female mice of strains C56BL/6J and DBA/2J. Mice of the parental strains, from recombinant inbred strains derived from these (BXD RI), and F(2) progeny were fed an atherogenic diet for 16 weeks, beginning at 1 year of age. This induced atherosclerotic lesion formation in both parental strains, accompanied by increased plasma LDL levels. However, individual BXD RI strains and the BXD F(2) mice demonstrated a range of atherosclerotic lesion formation that was not or at best weakly correlated with plasma lipid levels. Quantitative trait locus (QTL) analysis of the BXD F(2) mice identified a locus with significant linkage (lod 4.5) for aortic lesion size on Chromosome (Chr) 10 that was independent of plasma lipids. Other loci with suggestive or significant linkage for various plasma lipid measures were identified on Chr 2, 3, 4, 5, 6, 7, 11, and 17. In this intercross, the genes primarily influencing atherosclerosis are distinct from those controlling plasma lipid levels.
独立于影响血浆脂质水平的遗传因素是人类动脉粥样硬化风险的主要促成因素,然而其背后的机制却知之甚少。本研究检测了C56BL/6J和DBA/2J品系16月龄雌性小鼠的血浆脂质和饮食诱导的动脉粥样硬化。从这两个亲本品系衍生的重组近交系(BXD RI)以及F(2)子代的小鼠,从1岁开始喂食致动脉粥样硬化饮食16周。这在两个亲本品系中均诱导了动脉粥样硬化病变形成,同时伴有血浆低密度脂蛋白水平升高。然而,各个BXD RI品系和BXD F(2)小鼠表现出一系列动脉粥样硬化病变形成情况,这些情况与血浆脂质水平无相关性或最多只有微弱相关性。对BXD F(2)小鼠进行数量性状基因座(QTL)分析,在10号染色体(Chr)上确定了一个与主动脉病变大小有显著连锁关系(lod值为4.5)的基因座,该基因座独立于血浆脂质。在2号、3号、4号、5号、6号、7号、11号和17号染色体上还确定了其他与各种血浆脂质指标有提示性或显著连锁关系的基因座。在这个杂交组合中,主要影响动脉粥样硬化的基因与控制血浆脂质水平的基因不同。