Detection of a normally rare transcript in propionic acidemia patients with mRNA destabilizing mutations in the PCCA gene

被引:23
作者
Campeau, E
Dupuis, L
Leclere, D
Gravel, RA
机构
[1] McGill Univ, Montreal Childrens Hosp, Res Inst, Dept Biol, Montreal, PQ H3Z 2Z3, Canada
[2] McGill Univ, Montreal Childrens Hosp, Res Inst, Dept Human Genet, Montreal, PQ H3Z 2Z3, Canada
[3] McGill Univ, Montreal Childrens Hosp, Res Inst, Dept Pediat, Montreal, PQ H3Z 2Z3, Canada
关键词
D O I
10.1093/hmg/8.1.107
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Propionic acidemia is an autosomal recessive disorder caused by a deficiency in the mitochondrial enzyme propionyl-CoA carboxylase (PCC), PCC is composed of two subunits, alpha and beta, encoded by the PCCA and PCCB genes, respectively, We analyzed mutations of the PCCA gene using patients' fibroblasts diagnosed with alpha subunit deficiency. By RT-PCR, four of 12 cell lines examined appeared to have a larger transcript present at a level comparable with that of the expected normal species. Sequencing of the larger transcript revealed an 84 bp insertion at nt 1209 of the coding sequence. Its incorporation in the transcript results in translation termination due to the presence of two in-frame stop codons, The 84 bp insertion was found to originate from the intron between nt 1209 and 1210, Consensus splice donor and acceptor sites were found at the 3'- and 5'-ends of the insertion, respectively. The insertion was also found in the remaining eight cell lines as well as in normal cells, but at a much reduced level compared with the normal length sequence, Mutation analysis of the four cell lines showing seemingly elevated levels of the insertion sequence revealed one nonsense mutation (R288X), two frameshift deletions (700del5 and 1115del4) and one splice mutation (1671IVS+5G-->C) as expressed alleles, We conclude that the common characteristic of the four cell lines is that they contain mRNA destabilizing mutations that reduce the mRNA level of the normal length sequence. Consequently, the low levels of cryptic mRNAs become detectable at a level similar to that of the residual level of the normal length mRNA. We suggest that screening for an increased proportion of the 84 bp insertion by RT-PCR can be used as a rapid assay for RNA destabilizing mutations. Our results suggest caution in associating such mutations with aberrant mRNA species, such as cryptic splice products, which may instead be part of the 'background noise' of the splicing machinery.
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页码:107 / 113
页数:7
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