Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib)

E Schollen, L Dorland, T J de Koning, O P Van Diggelen, J G Huijmans, T Marquardt, D Babovic-Vuksanovic, M Patterson, F Imtiaz, B Winchester, M Adamowicz, E Pronicka, H Freeze, G Matthijs

Onderzoeksoutputpeer review

38 Citaten (Scopus)

Samenvatting

CDG-Ib is the "gastro-intestinal" type of the congenital disorders of glycosylation (CDG) and a potentially treatable disorder. It has been described in patients presenting with congenital hepatic fibrosis and protein losing enteropathy. The symptoms result from hypoglycosylation of serum- and other glycoproteins. CDG-Ib is caused by a deficiency of mannose-6-phosphate isomerase (synonym: phosphomannose isomerase, EC 5.3.1.8), due to mutations in the MPI gene. We determined the genomic structure of the MPI gene in order to simplify mutation detection. The gene is composed of 8 exons and spans only 5 kb. Eight (7 novel) different mutations were found in seven patients with a confirmed phosphomannose isomerase deficiency, analyzed in the context of this study: six missense mutations, a splice mutation and one insertion. In the last, the mutation resulted in an unstable transcript, and was hardly detectable at the mRNA level. This emphasizes the importance of mutation analysis at the genomic DNA level.

Originele taal-2English
Pagina's (van-tot)247-252
Aantal pagina's6
TijdschriftHuman Mutation
Volume16
Nummer van het tijdschrift3
DOI's
StatusPublished - sep.-2000
Extern gepubliceerdJa

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