The E5 proteins

被引:199
作者
DiMaio, Daniel [1 ,2 ,3 ]
Petti, Lisa M. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Genet, POB 208005, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Therapeut Radiol, New Haven, CT 06520 USA
[3] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
关键词
Papillomaviruses; Cervical cancer; Transmembrane proteins; PDGF receptor; Vacuolar ATPase; EGF receptor; HPV; HUMAN-PAPILLOMAVIRUS TYPE-16; GROWTH-FACTOR RECEPTOR; FACTOR-BETA RECEPTOR; MHC CLASS-I; VACUOLAR H+-ATPASE; OPEN READING FRAME; HUMAN FORESKIN KERATINOCYTES; MORTAL HUMAN FIBROBLASTS; FASL-MEDIATED APOPTOSIS; CELL-CYCLE PROGRESSION;
D O I
10.1016/j.virol.2013.05.006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The E5 proteins are short transmembrane proteins encoded by many animal and human papillomaviruses. These proteins display transforming activity in cultured cells and animals, and they presumably also play a role in the productive virus life cycle. The E5 proteins are thought to act by modulating the activity of cellular proteins. Here, we describe the biological activities of the best-studied E5 proteins and discuss the evidence implicating specific protein targets and pathways in mediating these activities. The primary target of the 44-amino acid BPV1 E5 protein is the PDGF beta receptor, whereas the EGF receptor appears to be an important target of the 83-amino acid HPV16 E5 protein. Both E5 proteins also bind to the vacuolar ATPase and affect MHC class I expression and cell-cell communication. Continued studies of the E5 proteins will elucidate important aspects of transmembrane protein- protein interactions, cellular signal transduction, cell biology, virus replication, and tumorigenesis. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:99 / 114
页数:16
相关论文
共 180 条
[21]   Mucosal human papillomaviruses encode four different E5 proteins whose chemistry and phylogeny correlate with malignant or benign growth [J].
Bravo, IG ;
Alonso, A .
JOURNAL OF VIROLOGY, 2004, 78 (24) :13613-13626
[22]   The human papillomavirus type 16 E5 protein alters vacuolar H+-ATPase function and stability in Saccharomyces cerevisiae [J].
Briggs, MW ;
Adam, JL ;
McCance, DJ .
VIROLOGY, 2001, 280 (02) :169-175
[23]   DNA-SEQUENCE OF THE HPV-16 E5 ORF AND THE STRUCTURAL CONSERVATION OF ITS ENCODED PROTEIN [J].
BUBB, V ;
MCCANCE, DJ ;
SCHLEGEL, R .
VIROLOGY, 1988, 163 (01) :243-246
[24]   GENETIC AND BIOCHEMICAL DEFINITION OF THE BOVINE PAPILLOMAVIRUS E5 TRANSFORMING PROTEIN [J].
BURKHARDT, A ;
DIMAIO, D ;
SCHLEGEL, R .
EMBO JOURNAL, 1987, 6 (08) :2381-2385
[25]   THE E5-ONCOPROTEIN OF BOVINE PAPILLOMAVIRUS IS ORIENTED ASYMMETRICALLY IN GOLGI AND PLASMA-MEMBRANES [J].
BURKHARDT, A ;
WILLINGHAM, M ;
GAY, C ;
JEANG, KT ;
SCHLEGEL, R .
VIROLOGY, 1989, 170 (01) :334-339
[26]   LOCALIZATION OF BOVINE PAPILLOMAVIRUS TYPE-1 E5 PROTEIN TO TRANSFORMED BASAL KERATINOCYTES AND PERMISSIVE DIFFERENTIATED CELLS IN FIBROPAPILLOMA TISSUE [J].
BURNETT, S ;
JAREBORG, N ;
DIMAIO, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) :5665-5669
[27]   Construction and genetic selection of small transmembrane proteins that activate the human erythropoietin receptor [J].
Cammett, Tobin J. ;
Jun, Susan J. ;
Cohen, Emily B. ;
Barrera, Francisco N. ;
Engelman, Donald M. ;
DiMaio, Daniel .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (08) :3447-3452
[28]   HPV-16 E5 down-regulates expression of surface HLA class I by CD8 T cells [J].
Campo, M. S. ;
Graham, S. V. ;
Cortese, M. S. ;
Ashrafi, G. H. ;
Araibi, E. H. ;
Dornan, E. S. ;
Miners, K. ;
Nunes, C. ;
Man, S. .
VIROLOGY, 2010, 407 (01) :137-142
[29]   Expression of a transforming gene (E5) of bovine papillomavirus in sarcoids obtained from horses [J].
Carr, EA ;
Théon, AP ;
Madewell, BR ;
Hitchcock, ME ;
Schlegel, R ;
Schiller, JT .
AMERICAN JOURNAL OF VETERINARY RESEARCH, 2001, 62 (08) :1212-1217
[30]   The expression of HPV-16 E5 protein in squamous neoplastic changes in the uterine cervix [J].
Chang, JL ;
Tsao, YP ;
Liu, DW ;
Huang, SJ ;
Lee, WH ;
Chen, SL .
JOURNAL OF BIOMEDICAL SCIENCE, 2001, 8 (02) :206-213