Association of the human papillomavirus type 16 E7 oncoprotein with the 600-kDa retinoblastoma protein-associated factor, p600

被引:142
作者
Huh, KW
DeMasi, J
Ogawa, H
Nakatani, Y
Howley, PM
Münger, K
机构
[1] Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
apoptosis; cervical carcinogensis; retinoblastoma tumor suppressor;
D O I
10.1073/pnas.0505337102
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 human papillomavirus type 16 (HPV-16) E7 gene encodes a multifunctional oncoprotein that can subvert multiple cellular regulatory pathways. The best-known cellular targets of the HPV-16 E7 oncoprotein are the retinoblastoma tumor suppressor protein pRB and the related pocket proteins p107 and p130. However, there is ample evidence that E7 has additional cellular targets that contribute to its transforming potential. We isolated HPV-16 E7 associated cellular protein complexes by tandem affinity purification and mass spectrometry and identified the 600-kDa retinoblastoma protein associated factor, p600, as a cellular target of E7. Association of E7 with p600 is independent of the pocket proteins and is mediated through the N terminal E7 domain, which is related to conserved region 1 of the adenovirus E1A protein and importantly contributes to cellular transformation independent of pRB binding. Depletion of p600 protein levels by RNA interference substantially decreased anchorage-independent growth in HPV-positive and -negative human cancer cells. Therefore, p600 is a cellular target of E7 that regulates cellular pathways that contribute to anchorage-independent growth and cellular transformation.
引用
收藏
页码:11492 / 11497
页数:6
相关论文
共 42 条
[1]   STRUCTURAL AND TRANSCRIPTIONAL ANALYSIS OF HUMAN PAPILLOMAVIRUS TYPE-16 SEQUENCES IN CERVICAL-CARCINOMA CELL-LINES [J].
BAKER, CC ;
PHELPS, WC ;
LINDGREN, V ;
BRAUN, MJ ;
GONDA, MA ;
HOWLEY, PM .
JOURNAL OF VIROLOGY, 1987, 61 (04) :962-971
[2]   Recapitulation of the effects of the human papillomavirus type 16 E7 oncogene on mouse epithelium by somatic Rb deletion and detection of pRb-independent effects of E7 in vivo [J].
Balsitis, SJ ;
Sage, J ;
Duensing, S ;
Münger, K ;
Jacks, T ;
Lambert, PF .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (24) :9094-9103
[3]  
BANKS L, 1990, ONCOGENE, V5, P1383
[4]  
Boyer SN, 1996, CANCER RES, V56, P4620
[5]   Stable suppression of tumorigenicity by virus-mediated RNA interference [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
CANCER CELL, 2002, 2 (03) :243-247
[6]   Bovine papillomavirus E7 transformation function correlates with cellular p600 protein binding [J].
DeMasi, J ;
Huh, KW ;
Nakatani, Y ;
Münger, K ;
Howley, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (32) :11486-11491
[7]   Mechanisms of genomic instability in human cancer:: Insights from studies with human papillomavirus oncoproteins [J].
Duensing, S ;
Münger, K .
INTERNATIONAL JOURNAL OF CANCER, 2004, 109 (02) :157-162
[8]   Human papillomavirus type 16 E7 oncoprotein can induce abnormal centrosome duplication through a mechanism independent of inactivation of retinoblastoma protein family members [J].
Duensing, S ;
Münger, K .
JOURNAL OF VIROLOGY, 2003, 77 (22) :12331-12335
[9]   A POINT MUTATIONAL ANALYSIS OF HUMAN PAPILLOMAVIRUS TYPE-16 E7-PROTEIN [J].
EDMONDS, C ;
VOUSDEN, KH .
JOURNAL OF VIROLOGY, 1989, 63 (06) :2650-2656
[10]   RING finger ubiquitin protein ligases: implications for tumorigenesis, metastasis and for molecular targets in cancer [J].
Fang, S ;
Lorick, KL ;
Jensen, JP ;
Weissman, AM .
SEMINARS IN CANCER BIOLOGY, 2003, 13 (01) :5-14