University Children's Hospital, Salzburger Landeskliniken (SALK) and Paracelsus Medical University (PMU), 5020 Salzburg, Austria; Institute of Human Genetics, Technical University München, 81675 Munich, Germany; Institute of Human Genetics, Helmholtz Zentrum, 85764 Neuherberg, Germany.
Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198 Gif-sur-Yvette, France.
Am J Hum Genet. 2020 Feb 6;106(2):256-263. doi: 10.1016/j.ajhg.2020.01.005. Epub 2020 Jan 30.
We report an inborn error of metabolism caused by TKFC deficiency in two unrelated families. Rapid trio genome sequencing in family 1 and exome sequencing in family 2 excluded known genetic etiologies, and further variant analysis identified rare homozygous variants in TKFC. TKFC encodes a bifunctional enzyme involved in fructose metabolism through its glyceraldehyde kinase activity and in the generation of riboflavin cyclic 4',5'-phosphate (cyclic FMN) through an FMN lyase domain. The TKFC homozygous variants reported here are located within the FMN lyase domain. Functional assays in yeast support the deleterious effect of these variants on protein function. Shared phenotypes between affected individuals with TKFC deficiency include cataracts and developmental delay, associated with cerebellar hypoplasia in one case. Further complications observed in two affected individuals included liver dysfunction and microcytic anemia, while one had fatal cardiomyopathy with lactic acidosis following a febrile illness. We postulate that deficiency of TKFC causes disruption of endogenous fructose metabolism leading to generation of by-products that can cause cataract. In line with this, an affected individual had mildly elevated urinary galactitol, which has been linked to cataract development in the galactosemias. Further, in light of a previously reported role of TKFC in regulating innate antiviral immunity through suppression of MDA5, we speculate that deficiency of TKFC leads to impaired innate immunity in response to viral illness, which may explain the fatal illness observed in the most severely affected individual.
我们报告了两例由 TKFC 缺乏引起的先天性代谢错误。在第 1 个家族中进行快速 trio 基因组测序,在第 2 个家族中进行外显子组测序,排除了已知的遗传病因,进一步的变异分析确定了 TKFC 中的罕见纯合变异。TKFC 编码一种多功能酶,通过其甘油醛激酶活性参与果糖代谢,并通过 FMN 裂合酶结构域生成核黄素环 4',5'-磷酸(环状 FMN)。这里报道的 TKFC 纯合变异位于 FMN 裂合酶结构域内。酵母中的功能测定支持这些变异对蛋白质功能的有害影响。TKFC 缺乏症患者的共同表型包括白内障和发育迟缓,在 1 例中与小脑发育不良有关。在 2 名受影响的个体中观察到的进一步并发症包括肝功能障碍和小细胞性贫血,而 1 名个体在发热性疾病后发生致命性心肌病伴乳酸酸中毒。我们推测 TKFC 缺乏会破坏内源性果糖代谢,导致产生的副产物可引起白内障。与此一致的是,一名受影响的个体尿液中的半乳糖醇略有升高,半乳糖醇与半乳糖血症中的白内障发展有关。此外,鉴于 TKFC 先前在通过抑制 MDA5 调节先天抗病毒免疫方面的作用,我们推测 TKFC 缺乏会导致对病毒病的先天免疫受损,这可能解释了最严重受影响个体中观察到的致命疾病。