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首页> 外文期刊>Physiological genomics >New Dyscalc loci for myocardial cell necrosis and calcification (dystrophic cardiac calcinosis) in mice
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New Dyscalc loci for myocardial cell necrosis and calcification (dystrophic cardiac calcinosis) in mice

机译:小鼠心肌细胞坏死和钙化(营养不良性心脏病)的新Dyscalc基因座

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摘要

Dystrophic cardiac calcinosis (DCC) occurs among certain inbred strains of mice and involves necrosis and subsequent calcification as response of myocardial tissue to injury. Using a complete linkage map approach, we investigated the genetics of DCC in an F_2 intercross of resistant C57BL/6J and susceptible C3H/HeJ inbred strains and identified previously a major predisposing quantitative trait locus (QTL), Dyscalc1, on proximal chromosome 7. Analysis of inheritance suggested, however, that DCC is influenced by additional modifier QTL, which have as yet not been mapped. Here, we report the identification by composite interval mapping of the DCC loci Dyscalc2, Dyscalc3, and Dyscalc4 on chromosomes 4, 12 and 14, respectively. Together, the four Dyscalc loci explained 47% of the phenotypic variance of DCC, which was induced by a high-fat diet. Additive epistasis between Dyscalc1 and Dyscalc2 enhanced DCC. Examining recombinant inbred strains, we propose a 10-cM interval containing Dyscalc1 and discuss potential candidate genes.
机译:营养不良性心脏钙化病(DCC)发生在某些近交系小鼠中,并涉及坏死和随后的钙化,作为心肌组织对损伤的反应。使用完整的连锁图谱方法,我们调查了抗性C57BL / 6J和易感C3H / HeJ自交系的F_2交配中DCC的遗传,并在近端第7号染色体上确定了先前的主要诱因数量性状基因位点Dyscalc1。但是,从继承的角度来看,DCC受尚未修改的其他修饰符QTL的影响。在这里,我们报告通过复合间隔映射分别在染色体4、12和14上的DCC基因座Dyscalc2,Dyscalc3和Dyscalc4的鉴定。四个Dyscalc基因座共同解释了DCC表型变异的47%,这是由高脂饮食诱导的。 Dyscalc1和Dyscalc2之间的加性上位增强了DCC。检查重组自交系,我们提出了一个包含Dyscalc1的10-cM区间,并讨论了潜在的候选基因。

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