Division of Public Health Sciences, Department of Epidemiology and Prevention, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Department of Urology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Sci Rep. 2020 Sep 28;10(1):15873. doi: 10.1038/s41598-020-71948-1.
Humans have undergone intense evolutionary selection to optimize their capacity to generate necessary quantities of long chain (LC-) polyunsaturated fatty acid (PUFA)-containing lipids. To better understand the impact of genetic variation within a locus of three FADS genes (FADS1, FADS2, and FADS3) on a diverse family of lipids, we examined the associations of 247 lipid metabolites (including four major classes of LC-PUFA-containing molecules and signaling molecules) with common and low-frequency genetic variants located within the FADS locus. Genetic variation in the FADS locus was strongly associated (p < 1.2 × 10) with 52 LC-PUFA-containing lipids and signaling molecules, including free fatty acids, phospholipids, lyso-phospholipids, and an endocannabinoid. Notably, the majority (80%) of FADS-associated lipids were not significantly associated with genetic variants outside of this FADS locus. These findings highlight the central role genetic variation at the FADS locus plays in regulating levels of physiologically critical LC-PUFA-containing lipids that participate in innate immunity, energy homeostasis, and brain development/function.
人类经历了强烈的进化选择,以优化其产生必需数量的长链(LC-)多不饱和脂肪酸(PUFA)脂质的能力。为了更好地理解三个 FADS 基因(FADS1、FADS2 和 FADS3)基因座内的遗传变异对多种脂质的影响,我们研究了 247 种脂质代谢物(包括四大类 LC-PUFA 分子和信号分子)与 FADS 基因座内常见和低频遗传变异的关联。FADS 基因座内的遗传变异与 52 种 LC-PUFA 脂质和信号分子强烈相关(p<1.2×10),包括游离脂肪酸、磷脂、溶血磷脂和内源性大麻素。值得注意的是,大多数(80%)与 FADS 相关的脂质与该 FADS 基因座之外的遗传变异没有显著关联。这些发现强调了 FADS 基因座内遗传变异在调节参与先天免疫、能量稳态和大脑发育/功能的生理关键 LC-PUFA 脂质水平方面的核心作用。