Autoregulation of Parkin activity through its ubiquitin-like domain

被引:261
作者
Chaugule, Viduth K. [1 ]
Burchell, Lynn [1 ]
Barber, Kathryn R. [2 ]
Sidhu, Ateesh [1 ]
Leslie, Simon J. [1 ]
Shaw, Gary S. [2 ]
Walden, Helen [1 ]
机构
[1] Canc Res UK, London Res Inst, Prot Struct & Funct Lab, London WC2A 3LY, England
[2] Univ Western Ontario, Dept Biochem, London, ON, Canada
关键词
ligase; Parkinson's disease; RING; ubiquitin; DISEASE GENE-PRODUCT; PROTEIN LIGASE; PATHOGENIC MUTATIONS; PROTECTIVE FUNCTION; INDEPENDENT UBIQUITINATION; CELL-DEATH; DEGRADATION; COMPLEX; PINK1; AGGREGATION;
D O I
10.1038/emboj.2011.204
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
Parkin is an E3-ubiquitin ligase belonging to the RBR (RING-InBetweenRING-RING family), and is involved in the neurodegenerative disorder Parkinson's disease. Autosomal recessive juvenile Parkinsonism, which is one of the most common familial forms of the disease, is directly linked to mutations in the parkin gene. However, the molecular mechanisms of Parkin dysfunction in the disease state remain to be established. We now demonstrate that the ubiquitin-like domain of Parkin functions to inhibit its autoubiquitination. Moreover pathogenic Parkin mutations disrupt this autoinhibition, resulting in a constitutively active molecule. In addition, we show that the mechanism of autoregulation involves ubiquitin binding by a C-terminal region of Parkin. Our observations provide important molecular insights into the underlying basis of Parkinson's disease, and in the regulation of RBR E3-ligase activity. The EMBO Journal ( 2011) 30, 2853-2867. doi:10.1038/emboj.2011.204; Published online 21 June 2011
引用
收藏
页码:2853 / 2867
页数:15
相关论文
共 76 条
  • [1] [Anonymous], DRUG DISCOVERY TODAY
  • [2] Proteasome inhibition and aggregation in Parkinson's disease: a comparative study in untransfected and transfected cells
    Biasini, E
    Fioriti, L
    Ceglia, I
    Invernizzi, R
    Bertoli, A
    Chiesa, R
    Forloni, G
    [J]. JOURNAL OF NEUROCHEMISTRY, 2004, 88 (03) : 545 - 553
  • [3] Regulation of E2F through ubiquitin-proteasome-dependent degradation: Stabilization by the pRB tumor suppressor protein
    Campanero, MR
    Flemington, EK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) : 2221 - 2226
  • [4] A MULTIUBIQUITIN CHAIN IS CONFINED TO SPECIFIC LYSINE IN A TARGETED SHORT-LIVED PROTEIN
    CHAU, V
    TOBIAS, JW
    BACHMAIR, A
    MARRIOTT, D
    ECKER, DJ
    GONDA, DK
    VARSHAVSKY, A
    [J]. SCIENCE, 1989, 243 (4898) : 1576 - 1583
  • [5] S-nitrosylation of Parkin regulates ubiquitination and compromises Parkin's protective function
    Chung, KKK
    Thomas, B
    Li, XJ
    Pletnikova, O
    Troncoso, JC
    Marsh, L
    Dawson, VL
    Dawson, TM
    [J]. SCIENCE, 2004, 304 (5675) : 1328 - 1331
  • [6] Identification of sites of ubiquitination in proteins: A Fourier transform ion cyclotron resonance mass spectrometry approach
    Cooper, HJ
    Heath, JK
    Jaffray, E
    Hay, RT
    Lam, TT
    Marshall, AG
    [J]. ANALYTICAL CHEMISTRY, 2004, 76 (23) : 6982 - 6988
  • [7] The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration
    Corti, O
    Hampe, C
    Koutnikova, H
    Darios, F
    Jacquier, S
    Prigent, A
    Robinson, JC
    Pradier, L
    Ruberg, M
    Mirande, M
    Hirsch, E
    Rooney, T
    Fournier, A
    Brice, A
    [J]. HUMAN MOLECULAR GENETICS, 2003, 12 (12) : 1427 - 1437
  • [8] The Role of Parkin in Familial and Sporadic Parkinson's Disease
    Dawson, Ted M.
    Dawson, Valina L.
    [J]. MOVEMENT DISORDERS, 2010, 25 (03) : S32 - S39
  • [9] Deleglio F., 1995, J BIOMOL NMR, V6, P277
  • [10] α-Synuclein and Parkin contribute to the assembly of ubiquitin lysine 63-linked multiubiquitin chains
    Doss-Pepe, EW
    Chen, L
    Madura, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (17) : 16619 - 16624