Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia

PubMed:View item in PubMed
Creators Name:Nuernberg, P. and Thiele, H. and Chandler, D. and Hoehne, W. and Cunningham, M.L. and Ritter, H. and Leschik, G. and Uhlmann, K. and Mischung, C. and Harrop, K. and Goldblatt, J. and Borochowitz, Z.U. and Kotzot, D. and Westermann, F. and Mundlos, S. and Braun, H.S. and Laing, N. and Tinschert, S.
Journal Title:Nature Genetics
Journal Abbreviation:Nat Genet
Volume:28
Number:1
Page Range:37-41
Date:1 January 2001
Keywords:Amino Acid Sequence, Amino Acid Sequence Homology, Ankylosis, Developmental Bone Diseases, Femur, Heterozygote, Knee, Membrane Proteins, Molecular Sequence Data, Mutation, Pedigree, Phosphate Transport Proteins, Skull
Abstract:Craniometaphyseal dysplasia (CMD) is a bone dysplasia characterized by overgrowth and sclerosis of the craniofacial bones and abnormal modeling of the metaphyses of the tubular bones. Hyperostosis and sclerosis of the skull may lead to cranial nerve compressions resulting in hearing loss and facial palsy1,2. An autosomal dominant form of the disorder (MIM 123000) was linked to chromosome 5p5.2-p14.1 (ref. 3) within a region harboring the human homolog (ANKH) of the mouse progressive ankylosis (ank) gene4. The ANK protein spans the outer cell membrane and shuttles inorganic pyrophosphate4 (PPi), a major inhibitor of physiologic and pathologic calcification, bone mineralization and bone resorption5. Here we carry out mutation analysis of ANKH, revealing six different mutations in eight of nine families. The mutations predict single amino acid substitutions, deletions or insertions. Using a helix prediction program, we propose for the ANK molecule 12 membrane-spanning helices with an alternate inside/out orientation and a central channel permitting the passage of PPi. The mutations occur at highly conserved amino acid residues presumed to be located in the cytosolic portion of the protein. Our results link the PPi channel ANK with bone formation and remodeling.
ISSN:1061-4036
Publisher:Nature Publishing Group (U.S.A.)
Item Type:Article

Repository Staff Only: item control page

Open Access
MDC Library