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

Authors :
Kamura T
Koepp DM
Conrad MN
Skowyra D
Moreland RJ
Iliopoulos O
Lane WS
Kaelin WG Jr
Elledge SJ
Conaway RC
Harper JW
Conaway JW
Source :
Science (New York, N.Y.) [Science] 1999 Apr 23; Vol. 284 (5414), pp. 657-61.
Publication Year :
1999

Abstract

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 G1 to S cell cycle transition. These findings provide a further link between VHL and the cellular ubiquitination machinery.

Details

Language :
English
ISSN :
0036-8075
Volume :
284
Issue :
5414
Database :
MEDLINE
Journal :
Science (New York, N.Y.)
Publication Type :
Academic Journal
Accession number :
10213691
Full Text :
https://doi.org/10.1126/science.284.5414.657