Swain-Lenz Devjanee, Nikolskiy Igor, Cheng Jiye, Sudarsanam Priya, Nayler Darcy, Staller Max V, Cohen Barak A
Center for Genome Sciences and Systems Biology, Washington University in St. Louis School of Medicine, Missouri 63110.
Department of Genetics, Washington University in St. Louis School of Medicine, Missouri 63110.
Genetics. 2017 Aug;206(4):2199-2206. doi: 10.1534/genetics.117.203752. Epub 2017 Jun 26.
An ongoing challenge in biology is to predict the phenotypes of individuals from their genotypes. Genetic variants that cause disease often change an individual's total metabolite profile, or metabolome. In light of our extensive knowledge of metabolic pathways, genetic variants that alter the metabolome may help predict novel phenotypes. To link genetic variants to changes in the metabolome, we studied natural variation in the yeast We used an untargeted mass spectrometry method to identify dozens of metabolite Quantitative Trait Loci (mQTL), genomic regions containing genetic variation that control differences in metabolite levels between individuals. We mapped differences in urea cycle metabolites to genetic variation in specific genes known to regulate amino acid biosynthesis. Our functional assays reveal that genetic variation in two genes, and , cause the differences in the abundance of several urea cycle metabolites. Based on knowledge of the urea cycle, we predicted and then validated a new phenotype: sensitivity to a particular class of amino acid isomers. Our results are a proof-of-concept that untargeted mass spectrometry can reveal links between natural genetic variants and metabolome diversity. The interpretability of our results demonstrates the promise of using genetic variants underlying natural differences in the metabolome to predict novel phenotypes from genotype.
生物学中一个长期存在的挑战是根据个体的基因型预测其表型。导致疾病的基因变异通常会改变个体的整体代谢物谱,即代谢组。鉴于我们对代谢途径的广泛了解,改变代谢组的基因变异可能有助于预测新的表型。为了将基因变异与代谢组的变化联系起来,我们研究了酵母中的自然变异。我们使用非靶向质谱方法来鉴定数十个代谢物数量性状位点(mQTL),即包含控制个体间代谢物水平差异的基因变异的基因组区域。我们将尿素循环代谢物的差异映射到已知调节氨基酸生物合成的特定基因的遗传变异上。我们的功能分析表明,两个基因(和)的遗传变异导致了几种尿素循环代谢物丰度的差异。基于对尿素循环的了解,我们预测并随后验证了一种新的表型:对特定一类氨基酸异构体的敏感性。我们的结果证明了非靶向质谱可以揭示自然遗传变异与代谢组多样性之间的联系这一概念。我们结果的可解释性证明了利用代谢组中自然差异背后的基因变异从基因型预测新表型的前景。