Rbx1, a component of the VHL tumor suppressor complex and SCF ubiquitin ligase

被引:660
作者
Kamura, T
Koepp, DM
Conrad, MN
Skowyra, D
Moreland, RJ
Iliopoulos, O
Lane, WS
Kaelin, WG
Elledge, SJ
Conaway, RC
Harper, JW
Conway, JW
机构
[1] Oklahoma Med Res Fdn, Howard Hughes Med Inst, Oklahoma City, OK 73104 USA
[2] Oklahoma Med Res Fdn, Howard Hughes Med Inst, Oklahoma City, OK 73104 USA
[3] Oklahoma Med Res Fdn, Program Mol & Cell Biol, Oklahoma City, OK 73104 USA
[4] Baylor Coll Med, Verna & Marrs McLean Dept Biochem, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[6] Harvard Univ, Brigham & Womens Hosp, Sch Med, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
[8] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[9] Harvard Univ, Harvard Microchem Facil, Cambridge, MA 02138 USA
[10] Univ Oklahoma, Hlth Sci Ctr, Dept Biochem & Mol Biol, Oklahoma City, OK 73190 USA
关键词
D O I
10.1126/science.284.5414.657
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The von Hippel-Lindau (VHL) tumor suppressor gene is mutated in most human kidney cancers. The VHL protein is part of a complex that includes Elongin B, Elongin C, and Cullin-2, proteins associated with transcriptional elongation and ubiquitination. Here it is shown that the endogenous VHL complex in rat liver also includes Rbx1, an evolutionarily conserved protein that contains a RING-H2 fingerlike motif and that interacts with Cullins. The yeast homolog of Rbx1 is a subunit and potent activator of the Cdc53-containing SCFCdc4 ubiquitin ligase required for ubiquitination of the cyclin-dependent kinase inhibitor Sic1 and for the G(1) to S cell cycle transition. These findings provide a further Link between VHL and the cellular ubiquitination machinery.
引用
收藏
页码:657 / 661
页数:5
相关论文
共 31 条
  • [21] A WORKBENCH FOR MULTIPLE ALIGNMENT CONSTRUCTION AND ANALYSIS
    SCHULER, GD
    ALTSCHUL, SF
    LIPMAN, DJ
    [J]. PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1991, 9 (03): : 180 - 190
  • [22] THE B-TYPE CYCLIN KINASE INHIBITOR P40(SIC1) CONTROLS THE G1 TO S TRANSITION IN SACCHAROMYCES-CEREVISIAE
    SCHWOB, E
    BOHM, T
    MENDENHALL, MD
    NASMYTH, K
    [J]. CELL, 1994, 79 (02) : 233 - 244
  • [23] Siemeister G, 1996, CANCER RES, V56, P2299
  • [24] F-box proteins are receptors that recruit phosphorylated substrates to the SCF ubiquitin-ligase complex
    Skowyra, D
    Craig, KL
    Tyers, M
    Elledge, SJ
    Harper, JW
    [J]. CELL, 1997, 91 (02) : 209 - 219
  • [25] Reconstitution of G1 cyclin ubiquitination with complexes containing SCFGrr1 and Rbx1
    Skowyra, D
    Koepp, DM
    Kamura, T
    Conrad, MN
    Conaway, RC
    Conaway, JW
    Elledge, SJ
    Harper, JW
    [J]. SCIENCE, 1999, 284 (5414) : 662 - 665
  • [26] Signal-induced ubiquitination of IκBα by the F-box protein Slimb/β-TrCP
    Spencer, E
    Jiang, J
    Chen, ZJJ
    [J]. GENES & DEVELOPMENT, 1999, 13 (03) : 284 - 294
  • [27] SIC1 is ubiquitinated in vitro by a pathway that requires CDC4, CDC34, and cyclin/CDK activities
    Verma, R
    Feldman, RMR
    Deshaies, RJ
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1997, 8 (08) : 1427 - 1437
  • [28] Cdc53 targets phosphorylated G1 cyclins for degradation by the ubiquitin proteolytic pathway
    Willems, AR
    Lanker, S
    Patton, EE
    Craig, KL
    Nason, TF
    Mathias, N
    Kobayashi, R
    Wittenberg, C
    Tyers, M
    [J]. CELL, 1996, 86 (03) : 453 - 463
  • [29] The SCFβ-TRCP-ubiquitin ligase complex associates specifically with phosphorylated destruction motifs in IκBα and β-catenin and stimulates IκBα ubiquitination in vitro
    Winston, JT
    Strack, P
    Beer-Romero, P
    Chu, CY
    Elledge, SJ
    Harper, JW
    [J]. GENES & DEVELOPMENT, 1999, 13 (03) : 270 - 283
  • [30] Identification of the receptor component of the IκBα-ubiquitin ligase
    Yaron, A
    Hatzubai, A
    Davis, M
    Lavon, I
    Amit, S
    Manning, AM
    Andersen, JS
    Mann, M
    Mercurio, F
    Ben-Neriah, Y
    [J]. NATURE, 1998, 396 (6711) : 590 - 594