Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy

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Serval ID
serval:BIB_1B7B96B25B4E
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
Journal
Human Molecular Genetics
Author(s)
Biswas  S., Munier  F. L., Yardley  J., Hart-Holden  N., Perveen  R., Cousin  P., Sutphin  J. E., Noble  B., Batterbury  M., Kielty  C., Hackett  A., Bonshek  R., Ridgway  A., McLeod  D., Sheffield  V. C., Stone  E. M., Schorderet  D. F., Black  G. C.
ISSN
0964-6906 (Print)
Publication state
Published
Issued date
10/2001
Volume
10
Number
21
Pages
2415-23
Notes
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S. --- Old month value: Oct 1
Abstract
Corneal clarity is maintained by its endothelium, which functions abnormally in the endothelial dystrophies, leading to corneal opacification. This group of conditions includes Fuchs' endothelial dystrophy of the cornea (FECD), one of the commonest indications for corneal transplantation performed in developed countries, posterior polymorphous dystrophy (PPCD) and the congenital hereditary endothelial dystrophies (CHED). A genome-wide search of a three-generation family with early-onset FECD demonstrated significant linkage with D1S2830 (Z(max) = 3.72, theta = 0.0). Refinement of the critical region defined a 6-7 cM interval of chromosome 1p34.3-p32 within which lies the COL8A2 gene. This encodes the 703 amino acid alpha2 chain of type VIII collagen, a short-chain collagen which is a component of endothelial basement membranes and which represented a strong candidate gene. Analysis of its coding sequence defined a missense mutation (gln455lys) within the triple helical domain of the protein in this family. Mutation analysis in patients with FECD and PPCD demonstrated further missense substitutions in familial and sporadic cases of FECD as well as in a single family with PPCD. This is the first description of the molecular basis of any of the corneal endothelial dystrophies or of mutations in type VIII collagen in association with human disease. This suggests that the underlying pathogenesis of FECD and PPCD may be related to disturbance of the role of type VIII collagen in influencing the terminal differentiation of the neural crest derived corneal endothelial cell.
Keywords
Amino Acid Sequence Base Sequence Chromosome Mapping Chromosomes, Human, Pair 1/genetics Collagen Type VIII/*genetics Corneal Dystrophies, Hereditary/*genetics/pathology DNA/chemistry/genetics Endothelium, Corneal/*pathology/ultrastructure Family Health Female Fuchs' Endothelial Dystrophy/*genetics/pathology Genes/genetics Haplotypes Humans Male Microsatellite Repeats Microscopy, Electron Molecular Sequence Data Mutation, Missense Pedigree Sequence Analysis, DNA
Pubmed
Web of science
Open Access
Yes
Create date
28/01/2008 13:58
Last modification date
25/09/2019 7:08
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