Desmosomal protein structure and function and the impact of disease-causing mutations

被引:11
|
作者
Mohammed, Fiyaz [1 ]
Chidgey, Martyn [2 ]
机构
[1] Univ Birmingham, Inst Immunol & Immunotherapy, Birmingham B15 27T, W Midlands, England
[2] Univ Birmingham, Inst Clin Sci, Birmingham B15 2TT, W Midlands, England
基金
英国惠康基金;
关键词
Desmosome; Cell-cell adhesion; Desmosomal  proteins; Disease-related missense mutations; Arrhythmogenic  right ventricular; cardiomyopathy; DESMOPLAKIN; BINDING; DOMAIN; ROLES;
D O I
10.1016/j.jsb.2021.107749
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this graphical review we focus on the structural characteristics of desmosomal proteins, their interactions with each other and with the intermediate filament cytoskeleton. The wealth of structural information that is now available allows predictions to be made about the pathogenic effect of disease-causing mutations. We have selected representative examples of missense mutations that are buried, semi-buried or surface exposed, and demonstrate how such variants could affect the structural fold of desmosomal proteins that are expressed in the heart. We explain how such alterations could compromise desmosomal adhesion, resulting in life threatening diseases including arrhythmogenic right ventricular cardiomyopathy.
引用
收藏
页数:7
相关论文
共 50 条
  • [41] Functional analysis of disease-causing mutations in human galactokinase
    Timson, DJ
    Reece, RJ
    EUROPEAN JOURNAL OF BIOCHEMISTRY, 2003, 270 (08): : 1767 - 1774
  • [42] Disease-Causing Mutations in the G Protein Gαs Subvert the Roles of GDP and GTP
    Hu, Qi
    Shokat, Kevan M.
    CELL, 2018, 173 (05) : 1254 - +
  • [43] Disease-causing mutations in the cellular retinaldehyde binding protein tighten and abolish ligand interactions
    Golovleva, I
    Bhattacharya, S
    Wu, ZP
    Shaw, N
    Yang, YW
    Andrabi, H
    West, KA
    Burstedt, MSI
    Forsman, K
    Holmgren, G
    Sandgren, O
    Noy, N
    Qin, J
    Crabb, JW
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (14) : 12397 - 12402
  • [44] Functional analysis of the neurofibromatosis type 2 protein by means of disease-causing point mutations
    Stokowski, RP
    Cox, DR
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (03) : 873 - 891
  • [45] Disease-causing missense mutations in the PHEX gene interfere with membrane targeting of the recombinant protein
    Sabbagh, Y
    Boileau, G
    DesGroseillers, L
    Tenenhouse, HS
    HUMAN MOLECULAR GENETICS, 2001, 10 (15) : 1539 - 1546
  • [46] Crystal structure of glycogen debranching enzyme and insights into its catalysis and disease-causing mutations
    Zhai, Liting
    Feng, Lingling
    Xia, Lin
    Yin, Huiyong
    Xiang, Song
    NATURE COMMUNICATIONS, 2016, 7
  • [47] Crystal structure of glycogen debranching enzyme and insights into its catalysis and disease-causing mutations
    Liting Zhai
    Lingling Feng
    Lin Xia
    Huiyong Yin
    Song Xiang
    Nature Communications, 7
  • [48] Crystal structure of glycogen debranching enzyme and insights into its catalysis and disease-causing mutations
    Zhai, Liting
    Feng, Lingling
    Xia, Lin
    Yin, Huiyong
    Xiang, Song
    NATURE COMMUNICATIONS, 2016, 7
  • [49] Effects of disease-causing mutations on catalytic activity of the Wilson disease protein ATP7B
    Huster, D
    Kuhne, A
    Lutsenko, S
    Mossner, J
    Caca, K
    HEPATOLOGY, 2005, 42 (04) : 457A - 457A
  • [50] Phosphorylation of ABCB4 Impacts Its Function: Insights From Disease-Causing Mutations
    Gautherot, Julien
    Delautier, Daniele
    Maubert, Marie-Anne
    Ait-Slimane, Tounsia
    Bolbach, Gerard
    Delaunay, Jean-Louis
    Durand-Schneider, Anne-Marie
    Firrincieli, Delphine
    Barbu, Veronique
    Chignard, Nicolas
    Housset, Chantal
    Maurice, Michele
    Falguieres, Thomas
    HEPATOLOGY, 2014, 60 (02) : 610 - 621