| Literature DB >> 12357473 |
David B Everman1, Cynthia F Bartels, Yue Yang, Niranjan Yanamandra, Frances R Goodman, J Roberto Mendoza-Londono, Ravi Savarirayan, Susan M White, John M Graham, Robert Peter Gale, Eva Svarch, William G Newman, Albert R Kleckers, Clair A Francomano, Vinukonda Govindaiah, Lalji Singh, Stuart Morrison, J Terrig Thomas, Matthew L Warman.
Abstract
Growth/differentiation factor-5 (GDF5), also known as cartilage-derived morphogenetic protein-1 (CDMP-1), is a secreted signaling molecule that participates in skeletal morphogenesis. Heterozygous mutations in GDF5, which maps to human chromosome 20, occur in individuals with autosomal dominant brachydactyly type C (BDC). Here we show that BDC is locus homogeneous by reporting a GDF5 frameshift mutation segregating with the phenotype in a family whose trait was initially thought to map to human chromosome 12. We also describe heterozygous mutations in nine additional probands/families with BDC and show nonpenetrance in a mutation carrier. Finally, we show that mutant GDF5 polypeptides containing missense mutations in their active domains do not efficiently form disulfide-linked dimers when expressed in vitro. These data support the hypothesis that BDC results from functional haploinsufficiency for GDF5. Copyright 2002 Wiley-Liss, Inc.Entities:
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Year: 2002 PMID: 12357473 DOI: 10.1002/ajmg.10777
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299