Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta.

Kwang Soo Lee, Hae Ryong Song, Tae Joon Cho, Hyon J. Kim, Tae Mi Lee, Hyun Seok Jin, Hyun Young Park, Seong Man Kang, Sung Chul Jung, Soo Kyung Koo

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

Mutations in the type I collagen genes COL1A1 and COL1A2 are responsible for the dominantly inherited connective tissue disorder osteogenesis imperfecta (OI). The severity of OI is diverse, ranging from perinatal lethality to a very mild phenotype that is characterized by normal stature and the absence of deformities. Although there have been several studies on the mutational spectra of COL1A1 and/or COL1A2 in Western populations, very few cases have been reported from Asia. In this study, we investigated 67 unrelated Korean probands with OI and used nucleotide sequence analysis to detect COL1A1 and COL1A2 mutations. Thirty-five different mutations were identified in the two genes, including 24 novel mutations. Among the 35 kinds of detected mutations, 15 were glycine substitutions (seven in COL1A1 and eight in COL1A2), one was a nonsense mutation, four were frameshift mutations in COL1A1, three were in-frame duplications in COL1A2, and 12 were splice site mutations (seven in COL1A1 and five in COL1A2). Until now, mutations in the COL1A1 and COL1A2 genes known to cause OI were unique and rarely repeated in other families. Interestingly, the c.982G>A (p.Gly328Ser) mutation in COL1A2 was found recurrently and was the causative mutation in five independent OI probands. Haplotype analysis of the COL1A2 gene revealed that four probands from five independent OI probands with c.982G>A (p.Gly328Ser) had a common haplotype. Our clinical data showed the heterogeneity even within a specific genotype, which suggested the complex expression of this disease.

Original languageEnglish
JournalHuman mutation.
Volume27
Issue number6
Publication statusPublished - 2006 Jun 1
Externally publishedYes

Fingerprint

Osteogenesis Imperfecta
Collagen Type I
Mutation
Genes
Haplotypes
alpha 2(I) collagen
Frameshift Mutation
Nonsense Codon
Connective Tissue
Glycine
Sequence Analysis
Genotype
Phenotype

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Lee, K. S., Song, H. R., Cho, T. J., Kim, H. J., Lee, T. M., Jin, H. S., ... Koo, S. K. (2006). Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta. Human mutation., 27(6).

Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta. / Lee, Kwang Soo; Song, Hae Ryong; Cho, Tae Joon; Kim, Hyon J.; Lee, Tae Mi; Jin, Hyun Seok; Park, Hyun Young; Kang, Seong Man; Jung, Sung Chul; Koo, Soo Kyung.

In: Human mutation., Vol. 27, No. 6, 01.06.2006.

Research output: Contribution to journalArticle

Lee, KS, Song, HR, Cho, TJ, Kim, HJ, Lee, TM, Jin, HS, Park, HY, Kang, SM, Jung, SC & Koo, SK 2006, 'Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta.', Human mutation., vol. 27, no. 6.
Lee, Kwang Soo ; Song, Hae Ryong ; Cho, Tae Joon ; Kim, Hyon J. ; Lee, Tae Mi ; Jin, Hyun Seok ; Park, Hyun Young ; Kang, Seong Man ; Jung, Sung Chul ; Koo, Soo Kyung. / Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta. In: Human mutation. 2006 ; Vol. 27, No. 6.
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