Substitution of cysteine for glycine at residue 415 of one allele of the alpha 1(I) chain of type I procollagen in type III/IV osteogenesis imperfecta. Issue 11 (November 1991)

• Record Type: Journal Article
• Authors: Nicholls, A C; Oliver, J; Renouf, D V; Keston, M; Pope, F M
• Is Part Of: Journal of medical genetics. Volume 28:Issue 11(1991)
• Page Start: 757
• Page End: 764
• Publication Date: 1991-11
• Subjects: Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.28.11.757
• Languages: English
• ISSNs: 1468-6244

Abstract

Abstract : We have examined the type I collagen in a patient with type III/IV osteogenesis imperfecta. Two forms of alpha 1(I) chain were produced, one normal and the other containing a cysteine residue within the triple helical domain of the molecule. Cysteine is not normally present in this domain of type I collagen. Peptide mapping experiments localised the mutation to peptide alpha 1(I)CB3 which spans residues 403 to 551 of the triple helix. Subsequent PCR amplification of cDNA covering this region followed by sequencing showed a G to T single base change in the GGC codon for glycine 415 generating TGC, the codon for cysteine. The effect of the mutation on the protein is to delay secretion from the cell, reduce the thermal stability of the molecule by 2 degrees C, and cause excessive post-translational modification of all chains in molecules containing one or more mutant alpha 1(I) chains. The clinical phenotype observed in this patient and the position of the mutation conform to the recent prediction of Starman et al that Gly----Cys mutations in the alpha 1(I) chain have a gradient of severity decreasing from the C-terminus to the N-terminus.