Department of Human Genetics, McGill University, Montreal, QC, Canada.
Mol Genet Metab. 2013 Sep-Oct;110(1-2):86-9. doi: 10.1016/j.ymgme.2013.04.020. Epub 2013 May 4.
Isolated methylmalonic aciduria (MMA) results either from a defect in the mitochondrial enzyme methylmalonylCoA mutase (MCM), or in the intracellular conversion of vitamin B12 (cobalamin) into its active coenzyme adenosylcobalamin (AdoCbl). Mutations in the MMAB gene affect the function of the enzyme ATP:cob(I)alamin adenosyltransferase (ATR) and the production of AdoCbl. Measurement of MCM function in cultured patient fibroblasts, followed by somatic cell complementation analysis in cases where MCM function is decreased, has classically been used to diagnose the cblB cobalamin disorder. A patient with persistent MMA, who could not be diagnosed using traditional somatic cell studies, was subsequently shown by sequencing in a clinical laboratory to contain two variants in the MMAB gene. This observation brings into question whether somatic cell studies have failed to diagnose other cblB patients with mild cellular phenotypes. A high resolution melting analysis (HRMA) assay was developed for the MMAB gene. It was used to scan 96 reference samples and two cohorts of patients: 42 patients diagnosed with cblB by complementation studies; and 181 patients with undiagnosed MMA. MMAB mutations, including one novel nonsense mutation (c.12 C>A [p.C4X]), were identified in all members of the cblB cohort. Four patients with undiagnosed MMA, including the index case described above, were found to contain variants in the MMAB gene: c.185C>T (p.T62M), c.394T>C (p.C132R), c.398C>T (p.S133F), c.521C>T (p.S174L), c.572G>A (p.R191Q). Only the index case was found to have two variants, suggesting that somatic cell studies diagnose almost all cblB patients.
孤立型甲基丙二酸血症(MMA)是由线粒体酶甲基丙二酰辅酶 A 变位酶(MCM)缺陷或维生素 B12(钴胺素)在细胞内转化为其活性辅酶腺苷钴胺素(AdoCbl)缺陷引起的。MMAB 基因突变影响酶 ATP:cob(I)alamin 腺苷转移酶(ATR)的功能和 AdoCbl 的产生。在培养的患者成纤维细胞中测量 MCM 功能,然后在 MCM 功能降低的情况下进行体细胞互补分析,经典地用于诊断 cblB 钴胺素疾病。一名持续性 MMA 患者无法通过传统体细胞研究进行诊断,随后在临床实验室通过测序发现该患者的 MMAB 基因中存在两个变体。这一观察结果引发了一个问题,即体细胞研究是否未能诊断出具有轻度细胞表型的其他 cblB 患者。开发了用于 MMAB 基因的高分辨率熔解分析(HRMA)检测。它用于扫描 96 个参考样本和两个患者队列:42 名通过互补研究诊断为 cblB 的患者;和 181 名未确诊的 MMA 患者。在 cblB 队列的所有成员中均发现 MMAB 突变,包括一个新的无义突变(c.12 C>A [p.C4X])。4 名未确诊的 MMA 患者,包括上述索引病例,被发现 MMAB 基因存在变体:c.185C>T(p.T62M),c.394T>C(p.C132R),c.398C>T(p.S133F),c.521C>T(p.S174L),c.572G>A(p.R191Q)。只有索引病例被发现有两个变体,这表明体细胞研究几乎可以诊断所有 cblB 患者。