| Literature DB >> 20861657 |
Lorenne Robert1, Audrey Sénéchal, Béatrice Bocquet, Laetitia Herbin, Gilles Chaudieu, Vasiliki Kalatzis, Catherine André, Christian P Hamel.
Abstract
Choroideremia is an X-linked, progressive photoreceptor degeneration disorder due to mutations in CHM. In addition to an atrophy of the outer retina, affected individuals present with a characteristic atrophy of the choroid. To search for a canine model, we screened the CHM gene of 37 dogs (22 breeds) with various forms of retinal dystrophies. We found 21 variations in 13 breeds (17 detected in only one breed and 4 shared by two or more) with 43% segregating in the same pedigree, a Great Dane female and a female offspring. Of particular interest were an exonic missense variation and a 3-bp intronic deletion near a splice acceptor site. However, although not detected in unrelated healthy Great Danes, these variants were nonpathogenic since they did not segregate with the disease phenotype in the pedigree. These results suggest that a CHM dog model may not be viable, as is the case for mouse and zebrafish.Entities:
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Year: 2010 PMID: 20861657 DOI: 10.1159/000313992
Source DB: PubMed Journal: Ophthalmic Res ISSN: 0030-3747 Impact factor: 2.892