Human Molecular Genetics Advance Access published online on July 26, 2007
Human Molecular Genetics, doi:10.1093/hmg/ddm195
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A novel dominant negative mutation in Gdf5 generated by ENU mutagenesis impairs joint formation and causes osteoarthritis in mice
1 Mouse Functional Genomics Research Group, RIKEN GSC, 3-1-1 Kouyadai, Tsukuba, Ibaraki, 305-0074 JAPAN Fax: +81-29-836-9017 Voice Phone: +81-29-836-9013 2 Department of Human Morphology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 shikata-cho, Okayama, 700-8558, Japan 3 Laboratory for Bone and Joint Diseases, SRC, RIKEN, 4-6-1 Shirokanedai, Minato-ku, 108-8639, Tokyo, Japan 4 Department of Radiology, Tokyo Metropolitan Kiyose Children's Hospital, 1-3-1 Umezono, Kiyose City, Tokyo, 204-8567, Japan 5 Department of Orthopaedic Surgery and Rehabilitation, Osaka Medical Center and Research Institute for Maternal and Child Health, 840 Murodou-cho, Izumi City, Osaka, 594-1101, Japan 6 Department of Orthopaedic Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 shikata-cho, Okayama, 700-8558, Japan 7 Population and Quantitative Genomics Team, RIKEN GSC, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama City, Kanagawa, 230-0045, Japan
* Corresponding author E-mail: hmasuya{at}gsc.riken.jp
Received May 11, 2007; Revised July 13, 2007; Accepted July 13, 2007
Growth and differentiation factor 5 (GDF5) has been implicated in chondrogenesis and joint formation, and an association of GDF5 and osteoarthritis (OA) has recently been reported. However, the in vivo function of GDF5 remains mostly unclarified. While various human GDF5 mutations and their phenotypic consequences have been described, only loss-of-function mutations that cause brachypodism (shortening and joint ankylosis of the digits) have been reported in mice. Here, we report a new Gdf5 allele derived from a large scale N-ethyl-N-nitrosourea (ENU) mutagenesis screen. This allele carries an amino acid substitution (W408R) in a highly conserved region of the active signaling domain of the GDF5 protein. The mutation is semidominant, showing brachypodism and ankylosis in heterozygotes, and much more severe brachypodism, ankylosis of the knee joint, and malformation with early-onset OA of the elbow joint in homozygotes. The mutant GDF5 protein is secreted and dimerizes normally, but inhibits the function of the wild-type GDF5 protein in a dominant-negative fashion. This study further highlights a critical role of GDF5 in joint formation and the development of OA, and this mouse should serve as a good model for OA.
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