Conjugation of the ubiquitin-like protein NEDD8 to cullin-2 is linked to von Hippel-Lindau tumor suppressor function

被引:101
作者
Liakopoulos, D
Büsgen, T
Brychzy, A
Jentsch, S
Pause, A
机构
[1] Univ Heidelberg, Zentrum Mol Biol, D-69120 Heidelberg, Germany
[2] Max Planck Inst Biochem, Mol Oncol Grp, D-82152 Martinsried, Germany
[3] Max Planck Inst Biochem, Dept Mol Cell Biol, D-82152 Martinsried, Germany
关键词
D O I
10.1073/pnas.96.10.5510
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 tumor suppressor protein pVHL assembles with cullin-2 (hCUL-2) and elongin B/C forming a protein complex, CBCVHL, that resembles SKP1-CDC53-F-box protein ubiquitin ligases. Here, we show that hCUL-2 is modified by the conserved ubiquitin-like protein NEDD8 and that NEDD8-hCUL-2 conjugates are part of CBCVHL complexes in vivo. Remarkably, the formation of these conjugates is stimulated by the pVHL tumor suppressor. A tumorigenic PVHL variant, however, is essentially deficient in this activity. Thus, Ligation of NEDD8 to hCUL-2 is linked to pVHL activity and may be important for pVHL tumor suppressor function.
引用
收藏
页码:5510 / 5515
页数:6
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