Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Hum Mol Genet. 2023 Jan 1;32(1):15-29. doi: 10.1093/hmg/ddac176.
Genetic variation in genes regulating metabolism may be advantageous in some settings but not others. The non-failing adult heart relies heavily on fatty acids as a fuel substrate and source of ATP. In contrast, the failing heart favors glucose as a fuel source. A bootstrap analysis for genes with deviant allele frequencies in cardiomyopathy cases versus controls identified the MTCH2 gene as having unusual variation. MTCH2 encodes an outer mitochondrial membrane protein, and prior genome-wide studies associated MTCH2 variants with body mass index, consistent with its role in metabolism. We identified the referent allele of rs1064608 (p.Pro290) as being overrepresented in cardiomyopathy cases compared to controls, and linkage disequilibrium analysis associated this variant with the MTCH2 cis eQTL rs10838738 and lower MTCH2 expression. To evaluate MTCH2, we knocked down Mtch in Drosophila heart tubes which produced a dilated and poorly functioning heart tube, reduced adiposity and shortened life span. Cardiac Mtch mutants generated more lactate at baseline, and they displayed impaired oxygen consumption in the presence of glucose but not palmitate. Treatment of cardiac Mtch mutants with dichloroacetate, a pyruvate dehydrogenase kinase inhibitor, reduced lactate and rescued lifespan. Deletion of MTCH2 in human cells similarly impaired oxygen consumption in the presence of glucose but not fatty acids. These data support a model in which MTCH2 reduction may be favorable when fatty acids are the major fuel source, favoring lean body mass. However, in settings like heart failure, where the heart shifts toward using more glucose, reduction of MTCH2 is maladaptive.
基因调控代谢的遗传变异在某些情况下可能是有利的,但在其他情况下则不然。正常成人心脏主要依赖脂肪酸作为燃料底物和 ATP 的来源。相比之下,衰竭的心脏则更喜欢葡萄糖作为燃料来源。对心肌病病例与对照组中具有异常等位基因频率的基因进行自举分析,确定 MTCH2 基因为具有异常变异的基因。MTCH2 编码一种线粒体外膜蛋白,先前的全基因组研究将 MTCH2 变体与体重指数相关联,这与其在代谢中的作用一致。我们确定了 rs1064608(p.Pro290)的参考等位基因在心肌病病例中比对照组更为常见,连锁不平衡分析将该变体与 MTCH2 cis eQTL rs10838738 和 MTCH2 表达降低相关联。为了评估 MTCH2,我们在果蝇心脏管中敲低了 Mtch,这导致心脏管扩张和功能不良,脂肪减少和寿命缩短。心脏 Mtch 突变体在基线时产生更多的乳酸,并且在存在葡萄糖但不存在棕榈酸时表现出氧消耗受损。用丙酮酸脱氢酶激酶抑制剂二氯乙酸处理心脏 Mtch 突变体可减少乳酸并挽救寿命。在人类细胞中删除 MTCH2 同样会损害在存在葡萄糖但不存在脂肪酸时的氧消耗。这些数据支持这样一种模型,即当脂肪酸是主要燃料来源时,MTCH2 的减少可能是有利的,有利于瘦体重。然而,在心衰等情况下,心脏转向更多地使用葡萄糖,MTCH2 的减少是适应不良的。