Department of Medicine/Division of Cardiology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Cell Metab. 2013 Jan 8;17(1):141-52. doi: 10.1016/j.cmet.2012.12.007.
Obesity is a highly heritable disease driven by complex interactions between genetic and environmental factors. Human genome-wide association studies (GWAS) have identified a number of loci contributing to obesity; however, a major limitation of these studies is the inability to assess environmental interactions common to obesity. Using a systems genetics approach, we measured obesity traits, global gene expression, and gut microbiota composition in response to a high-fat/high-sucrose (HF/HS) diet of more than 100 inbred strains of mice. Here we show that HF/HS feeding promotes robust, strain-specific changes in obesity that are not accounted for by food intake and provide evidence for a genetically determined set point for obesity. GWAS analysis identified 11 genome-wide significant loci associated with obesity traits, several of which overlap with loci identified in human studies. We also show strong relationships between genotype and gut microbiota plasticity during HF/HS feeding and identify gut microbial phylotypes associated with obesity.
肥胖是一种高度遗传性疾病,由遗传和环境因素之间的复杂相互作用驱动。人类全基因组关联研究(GWAS)已经确定了一些与肥胖有关的基因座;然而,这些研究的一个主要局限性是无法评估肥胖常见的环境相互作用。我们使用系统遗传学方法,在 100 多只近交系小鼠中测量了肥胖特征、全基因表达和肠道微生物群落组成,以响应高脂肪/高蔗糖(HF/HS)饮食。在这里,我们表明 HF/HS 喂养促进了肥胖的强大、特定于品系的变化,这些变化不能用食物摄入量来解释,并为肥胖的遗传决定设定点提供了证据。GWAS 分析确定了 11 个与肥胖特征相关的全基因组显著基因座,其中几个与人类研究中确定的基因座重叠。我们还表明,在 HF/HS 喂养期间基因型和肠道微生物群落可塑性之间存在很强的关系,并确定了与肥胖相关的肠道微生物分类群。