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Science 16 April 1999: Vol. 284. no. 5413, pp. 455 - 461 DOI: 10.1126/science.284.5413.455
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Research Articles
Structure of the VHL-ElonginC-ElonginB Complex: Implications for VHL Tumor Suppressor Function
Charles E. Stebbins,
1
William G. Kaelin Jr.,
2
Nikola P. Pavletich
3*
Mutation of the VHL tumor suppressor is associated with the
inherited von Hippel-Lindau (VHL) cancer syndrome and the
majority of kidney cancers. VHL binds the ElonginC-ElonginB complex and regulates levels of hypoxia-inducible proteins. The structure of the
ternary complex at 2.7 angstrom resolution shows two interfaces, one
between VHL and ElonginC and another between ElonginC and ElonginB.
Tumorigenic mutations frequently occur in a 35-residue domain of VHL
responsible for ElonginC binding. A mutational patch on a separate
domain of VHL indicates a second macromolecular binding site. The
structure extends the similarities to the SCF (Skp1-Cul1-F-box
protein) complex that targets proteins for degradation, supporting the
hypothesis that VHL may function in an analogous pathway.
1 Department of Biochemistry and Structural
Biology, Joan and Sanford I. Weill Graduate School of Medical Sciences,
Cornell University, New York, NY 10021, USA.
2 Dana-Farber Cancer Institute and Howard Hughes
Medical Institute, Harvard Medical School, Boston, MA 02115, USA.
3 Cellular Biochemistry and Biophysics Program and
Howard Hughes Medical Institute, Memorial Sloan-Kettering Cancer
Center, New York, NY 10021, USA.
*
To whom correspondence should be addressed.
Read the Full Text
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- Carboxyl-Terminal Transactivation Activity of Hypoxia-Inducible Factor 1{alpha} Is Governed by a von Hippel-Lindau Protein-Independent, Hydroxylation-Regulated Association with p300/CBP.
- N. Sang, J. Fang, V. Srinivas, I. Leshchinsky, and J. Caro (2002)
Mol. Cell. Biol.
22, 2984-2992
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- Low mitochondrial respiratory chain content correlates with tumor aggressiveness in renal cell carcinoma.
- H. Simonnet, N. Alazard, K. Pfeiffer, C. Gallou, C. Beroud, J. Demont, R. Bouvier, H. Schagger, and C. Godinot (2002)
Carcinogenesis
23, 759-768
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- Role of the von Hippel-Lindau Tumor Suppressor Gene in the Formation of {beta}1-Integrin Fibrillar Adhesions.
- M. A. Esteban-Barragan, P. Avila, M. Alvarez-Tejado, M. D. Gutierrez, A. Garcia-Pardo, F. Sanchez-Madrid, and M. O. Landazuri (2002)
Cancer Res.
62, 2929-2936
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- Diverse Effects of Mutations in Exon II of the von Hippel-Lindau (VHL) Tumor Suppressor Gene on the Interaction of pVHL with the Cytosolic Chaperonin and pVHL-Dependent Ubiquitin Ligase Activity.
- W. J. Hansen, M. Ohh, J. Moslehi, K. Kondo, W. G. Kaelin, and W. J. Welch (2002)
Mol. Cell. Biol.
22, 1947-1960
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- Erythropoietin, tumours and the von Hippel-Lindau gene: towards identification of mechanisms and dysfunction of oxygen sensing.
- M. S. Wiesener and K.-U. Eckardt (2002)
Nephrol. Dial. Transplant.
17, 356-359
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- Degradation of p53 by adenovirus E4orf6 and E1B55K proteins occurs via a novel mechanism involving a Cullin-containing complex.
- E. Querido, P. Blanchette, Q. Yan, T. Kamura, M. Morrison, D. Boivin, W. G. Kaelin, R. C. Conaway, J. W. Conaway, and P. E. Branton (2001)
Genes & Dev.
15, 3104-3117
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- The von Hippel-Lindau Tumor Suppressor Protein Mediates Ubiquitination of Activated Atypical Protein Kinase C.
- H. Okuda, K. Saitoh, S.-i. Hirai, K. Iwai, Y. Takaki, M. Baba, N. Minato, S. Ohno, and T. Shuin (2001)
J. Biol. Chem.
276, 43611-43617
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- The Von Hippel-Lindau Protein Interacts with Heteronuclear Ribonucleoprotein A2 and Regulates Its Expression.
- P. A. Pioli and W. F. C. Rigby (2001)
J. Biol. Chem.
276, 40346-40352
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- Endoplasmic Reticulum Stress Prolongs GH-Induced Janus Kinase (JAK2)/Signal Transducer and Activator of Transcription (STAT5) Signaling Pathway.
- A. Flores-Morales, L. Fernandez, E. Rico-Bautista, A. Umana, C. Negrin, J.-G. Zhang, and G. Norstedt (2001)
Mol. Endocrinol.
15, 1471-1483
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- Molecular Pathogenesis of the Von Hippel-Lindau Hereditary Cancer Syndrome: Implications for Oxygen Sensing.
- H. Yang and W. G. Kaelin Jr. (2001)
Cell Growth Differ.
12, 447-455
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