Identification and analysis of 21 novel disease-causing amino acid substitutions in the conserved part of ATP7A

L.B. Moller, J.T. Bukrinsky, Anne Mølgaard, M. Paulsen, C. Lund, Z. Tumer, S. Larsen, N. Horn

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    ATP7A encodes a copper. translocating ATPase that belongs to the large family of P-type ATPases. Eight conserved regions define the core of the P-type ATPase superfamily. We report here the identification of 21 novel missense mutations in the conserved part of ATP7A that encodes the residues p.V842-p.S1404. Using the coordinates of X-ray crystal structures of the sarcoplasmic reticulum Ca2+-ATPase, as determined in the presence and absence of Ca2+, we created structural homology models of ATP7A. By mapping the substituted residues onto the models, we found that these residues are more clustered three-dimensionally than expected from the primary sequence. The location of the substituted residues in conserved regions supports the functional similarities between the two types of P-type ATPases. An immunofluorescence analysis of Menkes fibroblasts suggested that the localization of a large number of the mutated ATP7A protein variants was correct. In the absence of copper, they were located in perinuclear regions of the cells, just like the wild type. However, two of the mutated ATP7A variants showed only partly correct localization, and in five cultures no ATP7A protein could be detected. These findings suggest that although a disease-causing mutation may indicate a functional significance of the affected residue, this is not always the case.
    Original languageEnglish
    JournalHuman Mutation
    Issue number2
    Pages (from-to)84-93
    Publication statusPublished - 2005


    • ATP7A
    • structure
    • localization
    • P-type ATPases
    • copper transport
    • stability
    • missense mutations

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