Covalent modification of all members of human cullin family proteins by NEDD8

被引:249
作者
Hori, T
Osaka, F
Chiba, T
Miyamoto, C
Okabayashi, K
Shimbara, N
Kato, S
Tanaka, K
机构
[1] Tokyo Metropolitan Inst Med Sci, Bunkyo Ku, Tokyo 1130021, Japan
[2] Hoffmann La Roche Inc, Nutley, NJ 07110 USA
[3] Japan Sci & Technol Corp, Sagami Chem Res Ctr, ERATO, Kato Cytoprot Network Project, Kanagawa 2290012, Japan
[4] Sumitomo Elect Ind Ltd, Biomed R&D Dept, Sakae Ku, Yokohama, Kanagawa 2448588, Japan
关键词
cullin; NEDD8; SCF; ubiquitin; ubiquitin-like protein;
D O I
10.1038/sj.onc.1203093
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
Recently we found that NEDD8, a ubiquitin-like protein, was linked covalently to human cullin-4A (abbreviated Cul-4A) by a new ubiquitin-related pathway that is analogous to but distinct from the ligating system for SUMO1, another ubiquitin-like protein. However, it remained unknown whether the other five members of the family of human cullin/Cdc53 proteins are modified by NEDD8, Here we report that all Hs-Cul family proteins, such as Cul-1, Cul-2, Cul-3, Cul-4B, and Cul-5, in addition to Cul-4A, were modified by covalent attachment of NEDD8 in rabbit reticulocyte lysates, Moreover, by comprehensive Northern-blot analyses, we examined multiple tissue distributions of the messages for all Cul-family proteins, NEDD8, and the NEDD8-ligating system consisting of APP-BP1/hUba3, and hUbc12, which function as E1- and E2-like enzymes, respectively, The expressions of Cul-1, Cul-2, and Cul-3 resembled each other and were apparently correlated to those of NEDD8 and the NEDD8-ligating system in various human cells and tissues. However, the mRNA levels of Cul-4A, Cul-4B, and Cul-5 differed considerably from each other as well as from other Cul-family proteins. The enhanced expression of all Cul-family proteins except Cul-5 was observed in a variety of tumor cell lines.
引用
收藏
页码:6829 / 6834
页数:6
相关论文
共 40 条
  • [1] Chen LC, 1998, CANCER RES, V58, P3677
  • [2] SUMO-1 modification of IκBα inhibits NF-κB activation
    Desterro, JMP
    Rodriguez, MS
    Hay, RT
    [J]. MOLECULAR CELL, 1998, 2 (02) : 233 - 239
  • [3] The Cdc4/34/53 pathway targets Cdc6p for proteolysis in budding yeast
    Drury, LS
    Perkins, G
    Diffley, JFX
    [J]. EMBO JOURNAL, 1997, 16 (19) : 5966 - 5976
  • [4] Cloning and expression analysis of a novel salicylate suppressible gene, Hs-CUL-3, a member of cullin/Cdc53 family
    Du, M
    Sansores-Garcia, L
    Zu, ZF
    Wu, KKY
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (38) : 24289 - 24292
  • [5] The role of protein stability in the cell cycle and cancer
    Elledge, SJ
    Harper, JW
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1998, 1377 (02): : M61 - M70
  • [6] A complex of Cdc4p, Skp1p, and Cdc53p/cullin catalyzes ubiquitination of the phosphorylated CDK inhibitor Sic1p
    Feldman, RMR
    Correll, CC
    Kaplan, KB
    Deshaies, RJ
    [J]. CELL, 1997, 91 (02) : 221 - 230
  • [7] THE TS41 MUTATION IN CHINESE-HAMSTER CELLS LEADS TO SUCCESSIVE S PHASES IN THE ABSENCE OF INTERVENING G2, M, AND G1
    HANDELI, S
    WEINTRAUB, H
    [J]. CELL, 1992, 71 (04) : 599 - 611
  • [8] Skipping into the E2F1-destruction pathway
    Harper, JW
    Elledge, SJ
    [J]. NATURE CELL BIOLOGY, 1999, 1 (01) : E5 - E7
  • [9] The F-box protein β-TrCP associates with phosphorylated β-catenin and regulates its activity in the cell
    Hart, M
    Concordet, JP
    Lassot, I
    Albert, I
    del los Santos, R
    Durand, H
    Perret, C
    Rubinfeld, B
    Margottin, F
    Benarous, R
    Polakis, P
    [J]. CURRENT BIOLOGY, 1999, 9 (04) : 207 - 210
  • [10] Ubiquitin-dependent degradation of IκBα is mediated by a ubiquitin ligase Skp1/Cul 1/F-box protein FWD1
    Hatakeyama, S
    Kitagawa, M
    Nakayama, K
    Shirane, M
    Matsumoto, M
    Hattori, K
    Higashi, H
    Nakano, H
    Okumura, K
    Onoé, K
    Good, RA
    Nakayama, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) : 3859 - 3863