Marquez Jonathan, Viviano Stephen, Rahman Fahmid, Strohbehn Samuel D, Allworth Aimee, Perez Norma, Saneto Russell P, Anna Scott, Penón Portmann Mónica, Blue Elizabeth E, Glass Ian A, Deniz Engin, Shelkowitz Emily
Division of Genetic Medicine, Department of Pediatrics, University of Washington and Seattle Children's Hospital, Seattle, Washington, USA.
Department of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA.
J Inherit Metab Dis. 2025 Jul;48(4):e70053. doi: 10.1002/jimd.70053.
Mitochondriopathies are a diverse group of disorders caused by disruption of typical mitochondrial function. Heterogenous in nature, many of these disorders arise due to variants in genes encoding key mitochondrial proteins involved in transcription and translation of mitochondrial machinery. One such gene, VARS2, encodes a mitochondrial aminoacyl-tRNA synthetase that catalyzes the attachment of valine to its cognate tRNA molecule. Bi-allelic variants in VARS2 have been linked to several forms of mitochondrial encephalopathies or cardiomyoencephalopathies. While associated clinical phenotypes vary, they can include developmental delays, axial hypotonia, limb spasticity, and epilepsy. Here, we describe three additional clinical cases of VARS2-related mitochondriopathy with sequencing-confirmed variants in VARS2 that illustrate the phenotypic variability of this disorder. These include three novel variants: Lys225Glu, Cys281Tyr, and Leu732Cysfs*29. We further assess the pathogenicity and severity of the effects of the variants underlying these cases in a Xenopus model of disease through assaying both cardiac function and brain size. In addition, we use this model of VARS2 loss of function to assess the therapeutic potential of previously proposed amino acid supplementation. Through this approach, we demonstrate that the beneficial effects of valine supplementation in VARS2 mitochondriopathy may be dependent on residual enzyme activity.
线粒体病是由典型线粒体功能破坏引起的一组多样的疾病。这些疾病本质上具有异质性,其中许多是由于参与线粒体机制转录和翻译的关键线粒体蛋白编码基因的变异所致。其中一个这样的基因VARS2,编码一种线粒体氨酰-tRNA合成酶,该酶催化缬氨酸与其同源tRNA分子的连接。VARS2中的双等位基因变异与几种形式的线粒体脑病或心肌脑病有关。虽然相关的临床表型各不相同,但可能包括发育迟缓、轴向肌张力减退、肢体痉挛和癫痫。在这里,我们描述了另外三例VARS2相关线粒体病的临床病例,其VARS2变异经测序确认,说明了这种疾病的表型变异性。这些变异包括三个新的变异:Lys225Glu、Cys281Tyr和Leu732Cysfs*29。我们通过检测心脏功能和脑大小,在非洲爪蟾疾病模型中进一步评估这些病例潜在变异的致病性和影响的严重程度。此外,我们利用这种VARS2功能丧失模型来评估先前提出的氨基酸补充疗法的治疗潜力。通过这种方法,我们证明缬氨酸补充对VARS2线粒体病的有益作用可能取决于残余酶活性。