| First Author | Reed V | Year | 1997 |
| Journal | Hum Mol Genet | Volume | 6 |
| Issue | 3 | Pages | 417-23 |
| PubMed ID | 9147645 | Mgi Jnum | J:38978 |
| Mgi Id | MGI:86364 | Doi | 10.1093/hmg/6.3.417 |
| Citation | Reed V, et al. (1997) Mutation analysis provides additional proof that mottled is the mouse homologue of Menkes' disease. Hum Mol Genet 6(3):417-23 |
| abstractText | Menkes' disease (MD) and occipital horn syndrome (OHS) are allelic X-linked disorders caused by mutations in the copper ion transporting ATPase, ATP7A, Genetic, phenotypic and biochemical data suggest that mottled mutants in the mouse, which range in severity and phenotype, are caused by mutations in Atp7a, the mouse homologue of ATP7A, As the only causal mutation in Atp7a has been reported in one very mild allele thought to be a model for OHS, Atp7a(Mo- blo) (mottled blotchy), we sequenced the entire 4.5 kb coding region of three other mottled mutants, two of which are thought to be models for classical MD (Atpa(Mo-br), Atpa(Mo-13H)) and one with a slightly milder phenotype (Atp7a(Mo-vbr). Although no causal mutation was found in Atp7a(Mo-13H), mutations which can be predicted to affect Atp7a function were identified in Atp7a(Mo-br) and Atp7a(Mo-vbr). A 6 bp deletion of nucleotides 2478-2483, which can be predicted to affect the correct processing of the protein, was found in Atp7a(Mo-br) and an A(3189)-->C nucleotide change, which results in lysine-->threonine amino acid substitution in the phosphorylation domain, was found in Atp7a(Mo-vbr), Thus we provide further proof that mottled mutants will provide excellent models for MD as well as OHS. |
