Department of Human Genetics, University of Chicago, Chicago, IL, USA.
Pritzker School of Medicine, University of Chicago, Chicago, IL, USA.
Nat Genet. 2023 Mar;55(3):461-470. doi: 10.1038/s41588-023-01306-0. Epub 2023 Feb 16.
Obesity-associated morbidity is exacerbated by abdominal obesity, which can be measured as the waist-to-hip ratio adjusted for the body mass index (WHRadjBMI). Here we identify genes associated with obesity and WHRadjBMI and characterize allele-sensitive enhancers that are predicted to regulate WHRadjBMI genes in women. We found that several waist-to-hip ratio-associated variants map within primate-specific Alu retrotransposons harboring a DNA motif associated with adipocyte differentiation. This suggests that a genetic component of adipose distribution in humans may involve co-option of retrotransposons as adipose enhancers. We evaluated the role of the strongest female WHRadjBMI-associated gene, SNX10, in adipose biology. We determined that it is required for human adipocyte differentiation and function and participates in diet-induced adipose expansion in female mice, but not males. Our data identify genes and regulatory mechanisms that underlie female-specific adipose distribution and mediate metabolic dysfunction in women.
与肥胖相关的发病率因腹型肥胖而加剧,腹型肥胖可以通过调整身体质量指数(WHRadjBMI)的腰臀比来衡量。在这里,我们确定了与肥胖和 WHRadjBMI 相关的基因,并描述了预测可调节女性 WHRadjBMI 基因的等位基因敏感增强子。我们发现,几个与腰臀比相关的变异体位于灵长类动物特异性的 Alu 反转录转座子内,这些反转录转座子含有与脂肪细胞分化相关的 DNA 基序。这表明人类脂肪分布的遗传成分可能涉及反转录转座子作为脂肪增强子的共选择。我们评估了女性 WHRadjBMI 相关基因中最强的 SNX10 在脂肪生物学中的作用。我们确定它是人类脂肪细胞分化和功能所必需的,并且参与了雌性小鼠而非雄性小鼠的饮食诱导的脂肪扩张。我们的数据确定了基因和调节机制,这些基因和调节机制是女性特有的脂肪分布的基础,并介导了女性的代谢功能障碍。