PMID: 8444468Feb 1, 1993Paper

A single amino acid deletion in the alpha 2(I) chain of type I collagen produces osteogenesis imperfecta type III

Human Genetics
K MolyneuxR Dalgleish

Abstract

RNase A protection analysis was used in the search for the cause of a non-lethal osteogenesis imperfecta (OI) phenotype (Sillence type III). Cleavage of the hybrid formed between a normal alpha 2(I) sequence and RNA isolated from the patient indicated the presence of a mismatch. The position of the mismatch was determined and the corresponding area of COL1A2 was amplified using the polymerase chain reaction. Sequencing of cloned amplified DNA revealed the deletion, which was not present in either parent, of the final three bases of exon 19 in one of the patient's two COL1A2 alleles. The deletion results in the loss of amino acid 255 (a valine encoded by the last codon of exon 19) of the triple helical region of half of the alpha 2(I) collagen chains but does not disrupt the splicing of the heterogeneous nuclear RNA (hnRNA). This provides further evidence that OI type III may result from autosomal dominant mutations rather than only from autosomal recessive mutations as had previously been believed.

Citations

Sep 29, 2000·Journal of Pediatric Orthopedics·A C BaitnerP E Di Cesare
Feb 23, 1999·Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research·A L BoskeyR D Blank
Feb 24, 2000·American Journal of Physical Anthropology·S I Fairgrieve, J E Molto

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