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Gene by environment QTL mapping through multiple trait analyses in blood pressure salt-sensitivity: identification of a novel QTL in rat chromosome 5

机译:血压盐敏感性中通过多性状分析通过环境QTL进行基因定位:鉴定大鼠染色体5中新的QTL

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Background The genetic mechanisms underlying interindividual blood pressure variation reflect the complex interplay of both genetic and environmental variables. The current standard statistical methods for detecting genes involved in the regulation mechanisms of complex traits are based on univariate analysis. Few studies have focused on the search for and understanding of quantitative trait loci responsible for gene × environmental interactions or multiple trait analysis. Composite interval mapping has been extended to multiple traits and may be an interesting approach to such a problem. Methods We used multiple-trait analysis for quantitative trait locus mapping of loci having different effects on systolic blood pressure with NaCl exposure. Animals studied were 188 rats, the progenies of an F2 rat intercross between the hypertensive and normotensive strain, genotyped in 179 polymorphic markers across the rat genome. To accommodate the correlational structure from measurements taken in the same animals, we applied univariate and multivariate strategies for analyzing the data. Results We detected a new quantitative train locus on a region close to marker R589 in chromosome 5 of the rat genome, not previously identified through serial analysis of individual traits. In addition, we were able to justify analytically the parametric restrictions in terms of regression coefficients responsible for the gain in precision with the adopted analytical approach. Conclusion Future work should focus on fine mapping and the identification of the causative variant responsible for this quantitative trait locus signal. The multivariable strategy might be valuable in the study of genetic determinants of interindividual variation of antihypertensive drug effectiveness.
机译:背景技术个体间血压变化的遗传机制反映了遗传和环境变量之间复杂的相互作用。当前用于检测涉及复杂性状调控机制的基因的标准统计方法是基于单变量分析。很少有研究集中在寻找和理解负责基因×环境相互作用或多重性状分析的数量性状基因座上。复合区间映射已扩展到多个特征,并且可能是解决此类问题的有趣方法。方法我们采用多性状分析法对NaCl暴露对收缩压有不同影响的基因座进行定量性状基因座作图。研究的动物为188只大鼠,即F2大鼠的后代,在高血压和正常血压菌株之间杂交,在大鼠基因组中用179个多态性标记进行基因分型。为了适应来自相同动物的测量值的相关结构,我们应用了单变量和多变量策略来分析数据。结果我们在大鼠基因组5号染色体上靠近标记R589的区域中检测到了一个新的定量火车基因座,该序列先前未通过对单个性状的序列分析确定。另外,我们能够采用所采用的分析方法,根据负责提高精度的回归系数,从理论上证明参数限制的合理性。结论今后的工作应集中在精细定位和确定引起该数量性状基因座信号的致病变异上。该多变量策略可能在研究降压药有效性个体差异的遗传决定因素中具有重要价值。

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