The Nedd4 family of E3 ubiquitin ligases: functional diversity within a common modular architecture

被引:416
作者
Ingham, RJ
Gish, G
Pawson, T
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5S 1A8, Canada
关键词
ubiquitination; Nedd4; E3 ubiquitin ligase; HECT; WW; C2;
D O I
10.1038/sj.onc.1207436
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
Neuronal precursor cell-expressed developmentally downregulated 4 (Nedd4) is the prototypical protein in a family of E3 ubiquitin ligases that have a common domain architecture. They are comprised of a catalytic C-terminal HECT domain and N-terminal C2 domain and WW domains responsible for cellular localization and substrate recognition. These proteins are found throughout eukaryotes and regulate diverse biological processes through the targeted degradation of proteins that generally have a PPxY motif for WW domain recognition, and are found in the nucleus and at the plasma membrane. Whereas the yeast Saccharomyces cerevisiae uses a single protein, Rsp5p, to carry out these functions, evolution has provided higher eukaryotes with several related Nedd4 proteins that appear to have specialized roles. In this review we discuss how knowledge of individual domain function has provided insight into the physiological roles of the Nedd4 proteins and describe recent results that suggest discrete functions for individual family members.
引用
收藏
页码:1972 / 1984
页数:13
相关论文
共 197 条
  • [1] Defective regulation of the epithelial Na+ channel by Nedd4 in Liddle's syndrome
    Abriel, H
    Loffing, J
    Rebhun, JF
    Pratt, JH
    Schild, L
    Horisberger, JD
    Rotin, D
    Staub, O
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (05) : 667 - 673
  • [2] c-Ski acts as a transcriptional co-repressor in transforming growth factor-β signaling through interaction with Smads
    Akiyoshi, S
    Inoue, H
    Hanai, J
    Kusanagi, K
    Nemoto, N
    Miyazono, K
    Kawabata, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (49) : 35269 - 35277
  • [3] Characterization of the interactions between Nedd4-2, ENaC, and sgk-1 using surface plasmon resonance
    Asher, C
    Sinha, I
    Garty, H
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1612 (01): : 59 - 64
  • [4] Characterization of interactions between Nedd4 and β and γENaC using surface plasmon resonance
    Asher, C
    Chigaev, A
    Garty, H
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 286 (05) : 1228 - 1231
  • [5] Smads as transcriptional co-modulators
    Attisano, L
    Wrana, JL
    [J]. CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (02) : 235 - 243
  • [6] A novel Pro-Arg motif recognized by WW domains
    Bedford, MT
    Sarbassova, D
    Xu, J
    Leder, P
    Yaffe, MB
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (14) : 10359 - 10369
  • [7] WW domain-mediated interactions reveal a spliceosome-associated protein that binds a third class of proline-rich motif: The proline glycine and methionine-rich motif
    Bedford, MT
    Reed, R
    Leder, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) : 10602 - 10607
  • [8] FBP WW domains and the Abl SH3 domain bind to a specific class of proline-rich ligands
    Bedford, MT
    Chan, DC
    Leder, P
    [J]. EMBO JOURNAL, 1997, 16 (09) : 2376 - 2383
  • [9] Properties and regulation of glutamine transporter SN1 by protein kinases SGK and PKB
    Boehmer, C
    Okur, F
    Setiawan, I
    Bröer, S
    Lang, F
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 306 (01) : 156 - 162
  • [10] MHC class I ubiquitination by a viral PHD/LAP finger protein
    Boname, JM
    Stevenson, PG
    [J]. IMMUNITY, 2001, 15 (04) : 627 - 636