Literature DB >> 12357473

The mutational spectrum of brachydactyly type C.

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.

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Year:  2002        PMID: 12357473     DOI: 10.1002/ajmg.10777

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  27 in total

1.  Dach2-Hdac9 signaling regulates reinnervation of muscle endplates.

Authors:  Peter C D Macpherson; Pershang Farshi; Daniel Goldman
Journal:  Development       Date:  2015-10-19       Impact factor: 6.868

2.  Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe.

Authors:  Luitgard M Graul-Neumann; Alexandra Deichsel; Ulrike Wille; Naseebullah Kakar; Randi Koll; Christian Bassir; Jamil Ahmad; Valerie Cormier-Daire; Stefan Mundlos; Christian Kubisch; Guntram Borck; Eva Klopocki; Thomas D Mueller; Sandra C Doelken; Petra Seemann
Journal:  Eur J Hum Genet       Date:  2013-10-16       Impact factor: 4.246

Review 3.  TGF-β Family Signaling in Connective Tissue and Skeletal Diseases.

Authors:  Elena Gallo MacFarlane; Julia Haupt; Harry C Dietz; Eileen M Shore
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-11-01       Impact factor: 10.005

4.  Familial Brachydactyly with Variable Expression in Three Family Members.

Authors:  Ankur Singh; Rajniti Prasad; Om Prakash Mishra
Journal:  Indian J Pediatr       Date:  2018-06-14       Impact factor: 1.967

5.  Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations?

Authors:  Katja Stange; Claus-Eric Ott; Mareen Schmidt-von Kegler; Gabriele Gillesen-Kaesbach; Stefan Mundlos; Katarina Dathe; Petra Seemann
Journal:  J Hum Genet       Date:  2015-05-21       Impact factor: 3.172

6.  Expression profiling of transforming growth factor beta superfamily genes in developing orofacial tissue.

Authors:  Partha Mukhopadhyay; Robert M Greene; M Michele Pisano
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2006-07

7.  A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2.

Authors:  K W Kjaer; H Eiberg; L Hansen; C B van der Hagen; K Rosendahl; N Tommerup; S Mundlos
Journal:  J Med Genet       Date:  2005-07-13       Impact factor: 6.318

8.  Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangism.

Authors:  Wei Yang; Lihua Cao; Wenli Liu; Li Jiang; Miao Sun; Dai Zhang; Shusen Wang; Wilson H Y Lo; Yang Luo; Xue Zhang
Journal:  J Hum Genet       Date:  2008-02-19       Impact factor: 3.172

9.  GDF5 is a second locus for multiple-synostosis syndrome.

Authors:  Katherine Dawson; Petra Seeman; Eiman Sebald; Lily King; Matthew Edwards; John Williams; Stephan Mundlos; Deborah Krakow
Journal:  Am J Hum Genet       Date:  2006-02-24       Impact factor: 11.025

10.  Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN.

Authors:  Petra Seemann; Anja Brehm; Jana König; Carsten Reissner; Sigmar Stricker; Pia Kuss; Julia Haupt; Stephanie Renninger; Joachim Nickel; Walter Sebald; Jay C Groppe; Frank Plöger; Jens Pohl; Mareen Schmidt-von Kegler; Maria Walther; Ingmar Gassner; Cristina Rusu; Andreas R Janecke; Katarina Dathe; Stefan Mundlos
Journal:  PLoS Genet       Date:  2009-11-26       Impact factor: 5.917

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