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 |
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Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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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. |
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ISSN: | 0036-8075 |