Clinical heterogeneity and molecular findings in five Polish patients with glycerol kinase deficiency: investigation of two splice site mutations with computerized splice junction analysis and Xp21 ge
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- 作者：Hellerud ; Christina ; Adamowicz ; Maciej ; Jurkiewicz ; Dorota ; Taybert ; Joanna ; Kubalska ; Jolanta ; et. al.
- 关键词：Adrenal hypoplasia ; Duchenne muscular dystrophy ; Glycerol kinase deficiency ; Heterozygote ; Insertion ; Mutation ; RT-PCR ; Splice junction analysis ; Splice site ; Xp21
- 刊名：Molecular Genetics and Metabolism
- 出版年：2003
- 出版时间：July, 2003
- 年：2003
- 卷：79
- 期：3
- 页码：149-159
- 全文大小：355 K
文摘
Five cases of glycerol kinase deficiency are presented with clinical, biochemical, and genetic results. Two had the glycerol kinase deficiency as part of an Xp21 contiguous gene deletion syndrome—complex form—and three had an isolated form of the enzyme deficiency. In these we found two splice site mutations (IVS1+4A>G, IVS9-1G>T) and one insertion (1393_1394insG). In patients with the complex form, a deletion of the DAX1, GK genes and the distal part of the DMD gene was found. A computerized study was performed to predict the effects of the splice site mutations. It showed that the IVS9-1G>T mutation substantially altered and removed the wild-type site and enhanced a cryptic site seven nucleotides downstream, and that the IVS1+4A>G diminished the strength of the wild-type donor site from strong to leaky. To verify these predictions, we developed an RT-PCR system with gene-specific primers that exclusively amplifies the Xp21 glycerol kinase gene transcript. Identification of individuals at risk is motivated by a need to avoid delay in a correct diagnosis. For reliable identification of heterozygotes for isolated glycerol kinase deficiency, knowledge of the specific mutation in the proband is required. This is easily obtained with the RT-PCR analyses developed in this study.