Human Papillomavirus Type 16 E7 Oncoprotein Associates with the Cullin 2 Ubiquitin Ligase Complex, Which Contributes to Degradation of the Retinoblastoma Tumor Suppressor

• DOI: 10.1128/jvi.00881-07
• Publication Date: 2007-07-04T00:41:06Z
• Authors: KyungWon Huh; Xiaobo Zhou; Hiroyuki Hayakawa; Je-Yoel Cho; Towia A. Libermann; Jianping Jin; J. Wade Harper; Karl Munger
• Keywords: 0301 basic medicine; 570; Human papillomavirus 16; Proteasome Endopeptidase Complex; Ubiquitin; Papillomavirus E7 Proteins; 610; Gene Expression; Uterine Cervical Neoplasms; Oncogene Proteins, Viral; Cell Transformation, Viral; Cullin Proteins; Retinoblastoma Protein; Cell Line; 3. Good health; 03 medical and health sciences; Humans; Female; Mouth Neoplasms; RNA Interference

ABSTRACT Human papillomavirus type 16 (HPV16) and other high-risk HPVs are etiologically linked to the development of cervical carcinomas and contribute to a number of other tumors of the anogenital tract, as well as oral cancers. The high-risk HPV E6 and E7 oncoproteins are consistently expressed in cervical cancer cells and are necessary for the induction and maintenance of the transformed phenotype. An important aspect of HPV16 E7's oncogenic activities is destabilization of the retinoblastoma tumor suppressor (pRB) through a ubiquitin/proteasome-dependent mechanism, although the exact molecular mechanism is unknown. Here, we report that HPV16 E7 is associated with an enzymatically active cullin 2 ubiquitin ligase complex and that the HPV16 E7/pRB complex contains cullin 2. Depletion of cullin 2 by RNA interference causes increased steady-state levels and stability of pRB in HPV16 E7-expressing cells, and ectopic expression of HPV16 E7 and the cullin 2 complex leads to pRB ubiquitination in vivo. Hence, we propose that the HPV16 E7-associated cullin 2 ubiquitin ligase complex contributes to aberrant degradation of the pRB tumor suppressor in HPV16 E7-expressing cells.