Document Detail


COL10A1 nonsense and frame-shift mutations have a gain-of-function effect on the growth plate in human and mouse metaphyseal chondrodysplasia type Schmid.
MedLine Citation:
PMID:  17403716     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Missense, nonsense and frame-shift mutations in the collagen X gene (COL10A1) result in metaphyseal chondrodysplasia type Schmid (MCDS). Complete degradation of mutant COL10A1 mRNA by nonsense-mediated decay in human MCDS cartilage implicates haploinsufficiency in the pathogenesis for nonsense mutations in vivo. However, the mechanism is unclear in situations where the mutant mRNA persist. We show that nonsense/frame-shift mutations can elicit a gain-of-function effect, affecting chondrocyte differentiation in the growth plate. In an MCDS proband, heterozygous for a p.Y663X nonsense mutation, the growth plate cartilage contained 64% wild-type and 36% mutant mRNA and the hypertrophic zone was disorganized and expanded. The in vitro translated mutant collagen X chains, which are truncated, were misfolded, unable to assemble into trimers and interfered with the assembly of normal alpha1(X) chains into trimers. Unlike Col10a1 null mutants, transgenic mice (FCdel) bearing the mouse equivalent of a human MCDS p.P620fsX621 mutation, displayed typical characteristics of MCDS with disproportionate shortening of limbs and early onset coxa vara. In FCdel mice, the degree of expansion of the hypertrophic zones was transgene-dosage dependent, being most severe in mice homozygous for the transgene. Chondrocytes in the lower region of the expanded hypertrophic zone expressed markers uncharacteristic of hypertrophic chondrocytes, indicating that differentiation was disrupted. Misfolded FCdel alpha1(X) chains were retained within the endoplasmic reticulum of hypertrophic chondrocytes, activating the unfolded protein response. Our findings provide strong in vivo evidence for a gain-of-function effect that is linked to the activation of endoplasmic reticulum-stress response and altered chondrocyte differentiation, as a possible molecular pathogenesis for MCDS.
Authors:
Matthew S P Ho; Kwok Yeung Tsang; Rebecca L K Lo; Miki Susic; Outi Mäkitie; Tori W Y Chan; Vivian C W Ng; David O Sillence; Raymond P Boot-Handford; Gary Gibson; Kenneth M C Cheung; William G Cole; Kathryn S E Cheah; Danny Chan
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2007-04-02
Journal Detail:
Title:  Human molecular genetics     Volume:  16     ISSN:  0964-6906     ISO Abbreviation:  Hum. Mol. Genet.     Publication Date:  2007 May 
Date Detail:
Created Date:  2007-05-16     Completed Date:  2007-08-06     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9208958     Medline TA:  Hum Mol Genet     Country:  England    
Other Details:
Languages:  eng     Pagination:  1201-15     Citation Subset:  IM    
Affiliation:
Department of Biochemistry, The University of Hong Kong, Pokfulam, Hong Kong, China.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Amino Acid Sequence
Animals
Base Sequence
Chondrocytes / metabolism
Codon, Nonsense*
Collagen Type X / biosynthesis,  genetics*
DNA / genetics
Frameshift Mutation*
Growth Plate / pathology
Humans
Male
Mice
Mice, Mutant Strains
Mice, Transgenic
Osteochondrodysplasias / genetics*,  metabolism,  pathology
Phenotype
RNA, Messenger / genetics
Sequence Deletion
Chemical
Reg. No./Substance:
0/Codon, Nonsense; 0/Collagen Type X; 0/RNA, Messenger; 9007-49-2/DNA

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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