Lack of an intronic Sp1 binding-site polymorphism at the collagen type I α1 gene in healthy Korean women

• Published in: Bone (New York, N.Y.) N.Y.), 1999-02, Vol.24 (2), p.135-137
• Main Authors: Han, K.O, Moon, I.G, Hwang, C.S, Choi, J.T, Yoon, H.K, Min, H.K, Han, I.K
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Bone density; Collagen; Diseases of the osteoarticular system; Genotype; Medical sciences; Osteoporosis; Osteoporosis. Osteomalacia. Paget disease; Polymorphism restriction fragment length
• ISSN: 8756-3282; 1873-2763
• DOI: 10.1016/S8756-3282(98)00155-0

Osteoporosis is a disease that is strongly genetically influenced. However, the genes responsible for the disease are poorly defined. Recent data show that a G-T transition polymorphism of the Sp1 binding site at the collagen type I α1 gene (Sp1 polymorphism) is associated significantly with bone mineral density (BMD) and osteoporotic fracture in British women. To establish the association between the Sp1 genotypes and BMD in Korean women, we examined 200 healthy postmenopausal women of Korean ethnicity, ranging in age from 44 to 66 years (mean ± SD: 54.7 ± 5.3 years). PCR amplification using the same primers as those used previously, with enzyme digestion, revealed no restriction site in our samples. We also performed a single-strand conformational polymorphism (SSCP) analysis in 100 of the 200 samples and could not find any polymorphic sites in the PCR amplification region. Based on our study, the Sp1 polymorphism at the type I collagen α1 gene was not found in Korean women. Therefore, we suggest that the Sp1 polymorphism at the type I collagen α1 gene is absent or rare in Korean women. Based on the present findings, this polymorphism does not seem to be responsible for the entire genetic contribution to BMD.