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

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...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 1999-04, Vol.284 (5414), p.658-661
Hauptverfasser: Kamura, T, Koepp, D M, Conrad, M N, Skowyra, D, Moreland, R J, Iliopoulos, O, Lane, W S, Kaelin, WG Jr, Elledge, S J, Conaway, R C, Harper, J W, Conaway, J W
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Sprache:eng
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Zusammenfassung: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 SCF super(Cdc4) ubiquitin ligase required for ubiquitination of the cyclin-dependent kinase inhibitor Sic1 and for the G sub(1) to S cell cycle transition. These findings provide a further link between VHL and the cellular ubiquitination machinery.
ISSN:0036-8075