An allele of COL9A2 associated with intervertebral disc disease

被引:246
作者
Annunen, S
Paassilta, P
Lohiniva, J
Perälä, M
Pihlajamaa, T
Karppinen, J
Tervonen, O
Kröger, H
Lähde, S
Vanharanta, H
Ryhänen, L
Göring, HHH
Ott, J
Prockop, DJ
Ala-Kokko, L [1 ]
机构
[1] Univ Oulu, Bioctr, Collagen Res Unit, SF-90220 Oulu, Finland
[2] Univ Oulu, Dept Biochem Med, SF-90220 Oulu, Finland
[3] Univ Oulu, Dept Phys Med & Rehabil, SF-90220 Oulu, Finland
[4] Univ Oulu, Dept Diagnost Radiol, SF-90220 Oulu, Finland
[5] Univ Oulu, Dept Internal Med, SF-90220 Oulu, Finland
[6] Univ Kuopio, Dept Surg, Kuopio 70211, Finland
[7] Columbia Univ, Dept Genet & Dev, New York, NY 10032 USA
[8] Rockefeller Univ, Lab Stat Genet, New York, NY 10021 USA
[9] MCP Hahnemann Univ, Ctr Gene Therapy, Philadelphia, PA 19102 USA
关键词
D O I
10.1126/science.285.5426.409
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intervertebral disc disease is one of the most common musculoskeletal disorders. A number of environmental and anthropometric risk factors may contribute to it, and recent reports have suggested the importance of genetic factors as well. The COL9A2 gene, which codes for one of the polypeptide chains of collagen IX that is expressed in the intervertebral disc, was screened for sequence variations in individuals with intervertebral disc disease. The analysis identified a putative disease-causing sequence variation that converted a codon for glutamine to one for tryptophan in six out of the 157 individuals but in none of 174 controls. The tryptophan allele cosegregated with the disease phenotype in the four families studied, giving a lod score (Logarithm of odds ratio) for linkage of 4.5, and subsequent linkage disequilibrium analysis conditional on linkage gave an additional lod score of 7.1.
引用
收藏
页码:409 / 412
页数:4
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