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在人类β-脲基丙酸酶基因UPB1中鉴定出一个影响前体mRNA剪接的新型同义突变。

Identification of a novel synonymous mutation in the human β -Ureidopropionase Gene UPB1 affecting pre-mRNA splicing.

作者信息

Meijer J, Nakajima Y, Zhang C, Meinsma R, Ito T, Van Kuilenburg A B P

机构信息

a Laboratory of Genetic Metabolic Diseases , Academic Medical Center , Amsterdam , The Netherlands.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2013;32(12):639-45. doi: 10.1080/15257770.2013.847189.

Abstract

β-Ureidopropionase is the third enzyme of the pyrimidine degradation pathway and it catalyzes the conversion of N-carbamyl-β-alanine and N-carbamyl-β-aminoisobutyric acid to β-alanine and β-aminoisobutyric acid, respectively, and ammonia and CO2. To date, only 16 genetically confirmed patients with a complete ß-ureidopropionase deficiency have been reported. Here, we report the clinical, biochemical, and molecular analysis of a newly identified patient with β-ureidopropionase deficiency. Mutation analysis of the UPB1 gene showed that the patient was compound heterozygous for a novel synonymous mutation c.93C >T (p.Gly31Gly) in exon 1 and a previously described missense mutation c.977G >A (p.Arg326Gln) in exon 9. The in silico predicted effect of the synonymous mutation p.Gly31Gly on pre-mRNA splicing was investigated using a minigene approach. Wild-type and the mutated minigene constructs, containing the entire exon 1, intron 1, and exon 2 of UPB1, yielded different splicing products after expression in HEK293 cells. The c.93C >T (p.Gly31Gly) mutation resulted in altered pre-mRNA splicing of the UPB1 minigene construct and a deletion of the last 13 nucleotides of exon 1. This deletion (r.92_104delGCAAGGAACTCAG) results in a frame shift and the generation of a premature stop codon (p.Lys32SerfsX31). Using a minigene approach, we have thus identified the first synonymous mutation in the UPB1 gene, creating a cryptic splice-donor site affecting pre-mRNA splicing.

摘要

β-脲基丙酸酶是嘧啶降解途径中的第三种酶,它催化N-氨甲酰基-β-丙氨酸和N-氨甲酰基-β-氨基异丁酸分别转化为β-丙氨酸和β-氨基异丁酸,以及氨和二氧化碳。迄今为止,仅报道了16例经基因确认的完全β-脲基丙酸酶缺乏症患者。在此,我们报告了一名新确诊的β-脲基丙酸酶缺乏症患者的临床、生化和分子分析情况。UPB1基因的突变分析显示,该患者为复合杂合子,外显子1存在一个新的同义突变c.93C>T(p.Gly31Gly),外显子9存在一个先前描述的错义突变c.977G>A(p.Arg326Gln)。使用小基因方法研究了同义突变p.Gly31Gly对前体mRNA剪接的计算机预测效应。包含UPB1完整外显子1、内含子1和外显子2的野生型和突变型小基因构建体在HEK293细胞中表达后产生了不同的剪接产物。c.93C>T(p.Gly31Gly)突变导致UPB1小基因构建体的前体mRNA剪接改变,外显子1最后13个核苷酸缺失。这种缺失(r.92_104delGCAAGGAACTCAG)导致移码并产生提前终止密码子(p.Lys32SerfsX31)。因此,我们通过小基因方法在UPB1基因中鉴定出首个同义突变,该突变产生了一个影响前体mRNA剪接的隐蔽剪接供体位点。

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