Genetic analysis of three genes causing isolated methylmalonic acidemia: identification of 21 novel allelic variants

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• 作者：Mart脙脙nez ; Maria Angeles ; Rinc脙脙n ; Ana ; Desviat ; Lourdes R. ; Merinero ; Bego脙脙a ; Ugarte ; Magdalena ; et. al.
• 关键词：Methylmalonic aciduria ; MMA ; Mutations ; Cobalamin ; cblA ; cblB ; MethylmalonylCoA mutase ; MCM
• 刊名：Molecular Genetics and Metabolism
• 出版年：2005
• 期刊代码：175_10967192
• 类别：bio
• 出版时间：April, 2005
• 卷：84
• 期：4
• 页码：317-325
• 文件大小：830 K

摘要

Isolated methylmalonic aciduria (MMA) is an inborn error of metabolism due to the impaired isomerization of l-methylmalonyl-CoA to succinyl-CoA. This reaction is catalyzed by the mitochondrial protein methylmalonyl-CoA mutase (MCM, EC 5.4.99.2), an adenosylcobalamin-dependent enzyme. Four different forms of isolated MMA have been described: mut MMA associated with defects in the MCM apoenzyme, and phenotypically divided into two subtypes mut⁻ and mut⁰ MMA, and three different defects involved in the synthesis of the active form of the cofactor adenosylcobalamin, termed cbl MMA, and classified into three different complementation groups cblA, cblB, and cblH associated with defects in the MMAA and MMAB genes and with an unidentified protein, respectively. In this work we describe the genetic analysis of 25 MMA patients, mainly from Spain. Using biochemical and cellular approaches our patients have been classified, identifying 13 mut MMA, 7 cblA, 2 cblB, and 3 noncblA, noncblB deficient patients. cDNA and genomic DNA sequence analysis of the MUT, MMAA, and MMAB genes have allowed us to identify 27 different changes, 21 novel ones. Among the missense mutations identified in the MUT gene only one, the c.970G > A (p.A324T) variant located in the substrate binding domain is likely a mut⁻ mutation. The remaining missense mutations c.326A > G (p.Q109R), c.983T > C (p.L328P), c.1846C > T (p.R616C), and c.1850T > G (p.L617R) are probably mut⁰. In the MMAA patients analyzed, frameshift mutations are prevalent. We have explored the genotype–phenotype correlation for this clinically heterogeneous disease.