Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH.
Institut de Recherches Cliniques de Montreal, Montreal, Canada.
J Lipid Res. 2013 Mar;54(3):816-822. doi: 10.1194/jlr.M034579. Epub 2012 Dec 17.
We used a mouse C57BL/6J×CASA/Rk intercross to map a locus on chromosome 14 that displayed a gender-dependent effect on cholesterol absorption from the intestine. Studies in congenic animals revealed a complex locus with multiple operating genetic determinants resulting in alternating gender-dependent phenotypic effects. Fine-mapping narrowed the locus to a critical 6.3 Mb interval. Female subcongenics, but not males, of the critical interval displayed a decrease of 33% in cholesterol absorption. RNA-Seq analysis of female subcongenic jejunum revealed that cysteine protease cathepsin B (Ctsb) is a candidate to explain the interval effect. Consistent with the phenotype in critical interval subcongenics, female Ctsb knockout mice, but not males, displayed a decrease of 31% in cholesterol absorption. Although studies in Ctsb knockouts revealed a gender-dependent effect on cholesterol absorption, further fine-mapping dismissed a role for Ctsb in determining the effect of the critical 6.3 Mb interval on cholesterol absorption.
我们利用 C57BL/6J×CASA/Rk 杂交鼠进行了基因定位研究,发现了一个位于 14 号染色体上的基因座,该基因座对肠道胆固醇吸收具有性别依赖性效应。在同系动物的研究中,发现了一个具有多个作用遗传决定因素的复杂基因座,这些遗传决定因素导致交替出现的性别依赖性表型效应。精细定位将该基因座缩小到一个关键的 6.3Mb 区间。关键区间的雌性亚系,但不是雄性,胆固醇吸收减少了 33%。对雌性亚系空肠的 RNA-Seq 分析表明,半胱氨酸蛋白酶组织蛋白酶 B(Ctsb)是解释该区间效应的候选基因。与关键区间亚系的表型一致,雌性 Ctsb 基因敲除小鼠,而不是雄性,胆固醇吸收减少了 31%。尽管 Ctsb 基因敲除小鼠的研究显示胆固醇吸收存在性别依赖性效应,但进一步的精细定位排除了 Ctsb 在决定关键的 6.3Mb 区间对胆固醇吸收影响中的作用。