首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Loci on chromosomes 14 and 2 distinct from ABCG5/ABCG8 regulate plasma plant sterol levels in a C57BL/6J × CASA/Rk intercross
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Loci on chromosomes 14 and 2 distinct from ABCG5/ABCG8 regulate plasma plant sterol levels in a C57BL/6J × CASA/Rk intercross

机译:与ABCG5 / ABCG8不同的14号和2号染色体上的基因座可调节C57BL / 6J×CASA / Rk互交的血浆植物固醇水平

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摘要

Plasma plant sterol levels differ among humans due to genetic and dietary factors. A disease characterized by high plasma plant sterol levels, β-sitosterolemia, was recently found to be due to mutations at the ABCG5/ABCG8 locus. To detect variants at this and other loci, a genetic cross was carried out between two laboratory mouse strains. Parental C57BL/6J had almost twice the campesterol and sitosterol levels compared with parental CASA/Rk mice, and F1 mice had levels halfway between the parentals. An intercross between F1s was performed and plasma plant sterol levels measured in 102 male and 99 female F2 mice. Plasma plant sterols in F2s displayed a unimodal distribution, suggesting the effects of several rather a single major gene. In the F2 mice, a full genome scan revealed significant linkages on chromosomes 14 and 2. With regard to chromosome 14, analysis showed a single peak for linkage at 17 cM with a logarithm of odds (LOD) score of 9.9, designated plasma plant sterol 14 (Plast14). With regard to chromosome 2, analysis showed two significant peaks for linkage at 18 and 65 cMs with LOD scores of 4.1 and 3.65, respectively, designated Plast2a and Plast2b, respectively. Four interactions between loci, predominantly of an additive nature, were also demonstrated, the most significant between Plast14 and Plast2b (LOD 16.44). No significant linkage or gene interaction was detected for the ABCG5/ABCG8 locus on chromosome 17. Therefore, other genes besides ABCG5/ABCG8 influence plasma plant sterol levels and now become candidates to explain differences in plasma plant sterol levels between humans.
机译:由于遗传和饮食因素,人体内血浆植物固醇水平不同。最近发现一种以血浆植物固醇水平较高为特征的疾病,即β-谷固醇血症,是由于ABCG5 / ABCG8基因座处的突变引起的。为了检测该位点和其他位点的变异,在两个实验室小鼠品系之间进行了遗传杂交。与亲本CASA / Rk小鼠相比,亲本C57BL / 6J的油菜甾醇和谷甾醇水平几乎是其两倍,而F1小鼠的亲和水平介于亲本之间。在102只雄性和99只雌性F2小鼠中进行了F1之间的杂交,并测量了血浆植物固醇水平。 F2s中的血浆植物固醇显示出单峰分布,提示了几个而不是单个主要基因的作用。在F2小鼠中,全基因组扫描显示了14号和2号染色体上的显着连锁。关于14号染色体,分析显示在17 cM处有一个单连锁峰,赔率(LOD)得分为9.9的对数,指定为血浆植物固醇14(Plast14)。关于2号染色体,分析显示在18和65 cMs有两个显着的连锁峰,LOD得分分别为4.1和3.65,分别称为Plast2a和Plast2b。还显示了基因座之间的四个相互作用,主要是累加性质,在Plast14和Plast2b之间最显着(LOD 16.44)。没有检测到17号染色​​体上ABCG5 / ABCG8基因座的显着连锁或基因相互作用。因此,除ABCG5 / ABCG8以外的其他基因影响血浆植物固醇水平,现在成为解释人类血浆植物固醇水平差异的候选者。

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