A functional polymorphism in COL11A1, which encodes the alpha 1 chain of type XI collagen, is associated with susceptibility to lumbar disc herniation
- PMID: 17999364
- PMCID: PMC2276353
- DOI: 10.1086/522377
A functional polymorphism in COL11A1, which encodes the alpha 1 chain of type XI collagen, is associated with susceptibility to lumbar disc herniation
Abstract
Lumbar disc herniation (LDH), degeneration and herniation of the nucleus pulposus of the intervertebral disc (IVD) of the lumbar spine, is one of the most common musculoskeletal diseases. Its etiology and pathogenesis, however, remain unclear. Type XI collagen is important for cartilage collagen formation and for organization of the extracellular matrix. We identified an association between one of the type XI collagen genes, COL11A1, and LDH in Japanese populations. COL11A1, which encodes the alpha 1 chain of type XI collagen, was highly expressed in IVD, but its expression was decreased in the IVD of patients with LDH. The expression level was inversely correlated with the severity of disc degeneration. A single-nucleotide polymorphism (c.4603C-->T [rs1676486]) had the most significant association with LDH (P=3.3 x 10(-6)), and the transcript containing the disease-associated allele was decreased because of its decreased stability. These observations indicate that type XI collagen is critical for IVD metabolism and that its decrease is related to LDH.
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References
Web Resources
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- Applied Biosystems, http://www.appliedbiosystems.com/index.cfm
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- GenBank, http://www.ncbi.nlm.nih.gov/Genbank/ (for COL11A1 sequences [accession numbers NM001854.2, AC093150.4, AL627203.7, and AC099567.2])
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- International HapMap Project, http://hapmap.org/
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- JSNP Database, http://snp.ims.u-tokyo.ac.jp/index.html
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- Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/ (for Stickler syndrome type II, Marshall syndrome, and oto-spondylo-mega-epiphyseal dysplasia)
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