Peng Hui, Lam Ying-Wai, Lau Kwok-Fai, Zhou Zitao, Herdt Aimee R, Gelb Michael H, Lee Chris W
Biomedical Research Institute of New Jersey (BRInj), Cedar Knolls, New Jersey, USA; Atlantic Health System, Morristown, New Jersey, USA; MidAtlantic Neonatology Associates (MANA), Morristown, New Jersey, USA.
Department of Biology & Vermont Biomedical Research Network Proteomics Facility, University of Vermont, Burlington, Vermont, USA.
J Biol Chem. 2025 May 29;301(7):110315. doi: 10.1016/j.jbc.2025.110315.
Krabbe disease is an autosomal recessive, demyelinating disorder caused by mutations in the GALC gene. Missense mutation variants (MMVs) account for most pathogenic alleles in patients; however, their mechanistic implications and correlations to clinical phenotype remain unclear. To address these questions, we generated a GALC knockout human oligodendrocytic cell line to conduct a robust GALC-MMVs expression study using a panel of 31 GALC-MMVs. Twenty-six clinically relevant variants dramatically reduced enzyme activity (92-100%). Notably, residual GALC activity strongly correlated with the age of disease-onset in reported cases (Pearson's r > 0.94, p < 0.0001), suggesting that enzyme activity resulting from MMV expression in this model may serve as a readout for clinical prognostication. In addition, we identified p.I562T, a predominant pseudodeficiency variant in the newborn screening programs, which synergistically impairs protein function and likely triggers disease-onset when inherited co-allelic with certain MMVs. We also identified MMVs that increased protein retention intracellularly and/or decreased secretion. This quantitative analysis of misfolding characteristics could be valuable for identifying MMVs amenable to pharmacological chaperone therapy. Finally, we observed an inverse correlation between residual GALC activity and endogenous psychosine levels in the MMV panel. Given the importance of psychosine as a biomarker for diagnosis and newborn screening, the psychosine accumulation phenotype in our model highlights its potential use for drug discovery. Overall, this study provides a comprehensive overview of the functional deficits and mis-trafficking caused by GALC-MMVs, deepens our understanding of molecular genetics and genotype-phenotype correlations in Krabbe disease, and highlights the potential of our platform for genetic and therapeutic applications.
克拉伯病是一种常染色体隐性脱髓鞘疾病,由GALC基因突变引起。错义突变变体(MMV)占患者中大多数致病等位基因;然而,它们的机制影响以及与临床表型的相关性仍不清楚。为了解决这些问题,我们生成了一个GALC基因敲除的人少突胶质细胞系,以使用一组31个GALC-MMV进行强有力的GALC-MMV表达研究。26个临床相关变体显著降低了酶活性(92%-100%)。值得注意的是,残余的GALC活性与报告病例中的疾病发病年龄密切相关(皮尔逊相关系数r>0.94,p<0.0001),这表明该模型中MMV表达产生的酶活性可能作为临床预后的一个指标。此外,我们鉴定出p.I562T,这是新生儿筛查项目中一种主要的假缺陷变体,当与某些MMV共等位遗传时,它会协同损害蛋白质功能并可能引发疾病发作。我们还鉴定出了在细胞内增加蛋白质滞留和/或减少分泌的MMV。这种对错误折叠特征的定量分析对于鉴定适合药物伴侣疗法的MMV可能很有价值。最后,我们在MMV组中观察到残余GALC活性与内源性半乳糖鞘氨醇水平之间呈负相关。鉴于半乳糖鞘氨醇作为诊断和新生儿筛查生物标志物的重要性,我们模型中的半乳糖鞘氨醇积累表型突出了其在药物发现中的潜在用途。总体而言,本研究全面概述了GALC-MMV引起的功能缺陷和错误转运,加深了我们对克拉伯病分子遗传学和基因型-表型相关性的理解,并突出了我们平台在基因和治疗应用方面的潜力。