Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai National Center for Translational Medicine, Shanghai, China.
Nat Metab. 2023 Aug;5(8):1337-1351. doi: 10.1038/s42255-023-00847-2. Epub 2023 Jul 17.
One lead genetic risk signal of obesity-the rs1421085 T>C variant within the FTO gene-is reported to be functional in vitro but lacks evidence at an organism level. Here we recapitulate the homologous human variant in mice with global and brown adipocyte-specific variant knock-in and reveal that mice carrying the C-allele show increased brown fat thermogenic capacity and resistance to high-fat diet-induced adiposity, whereas the obesity-related phenotypic changes are blunted at thermoneutrality. Both in vivo and in vitro data reveal that the C-allele in brown adipocytes enhances the transcription of the Fto gene, which is associated with stronger chromatin looping linking the enhancer region and Fto promoter. Moreover, FTO knockdown or inhibition effectively eliminates the increased thermogenic ability of brown adipocytes carrying the C-allele. Taken together, these findings identify rs1421085 T>C as a functional variant promoting brown fat thermogenesis.
肥胖的一个主要遗传风险信号——FTO 基因内的 rs1421085 T>C 变体——据报道在体外具有功能,但在机体水平缺乏证据。在这里,我们在小鼠中 recapitulate 了同源的人类变体,具有全局和棕色脂肪细胞特异性变体敲入,并揭示携带 C 等位基因的小鼠表现出增加的棕色脂肪产热能力和对高脂肪饮食诱导肥胖的抵抗力,而与肥胖相关的表型变化在常温下减弱。体内和体外数据均表明,棕色脂肪细胞中的 C 等位基因增强了 Fto 基因的转录,这与增强的染色质环连接增强子区域和 Fto 启动子有关。此外,FTO 敲低或抑制可有效消除携带 C 等位基因的棕色脂肪细胞产热能力的增加。总之,这些发现确定 rs1421085 T>C 是促进棕色脂肪产热的功能性变体。