The S phase of the cell cycle and its perturbation by human cytomegalovirus

被引:24
作者
Bain, Mark [1 ]
Sinclair, John [1 ]
机构
[1] Univ Cambridge, Addenbrookes Hosp, Sch Clin, Dept Med, Cambridge CB2 2QQ, England
基金
英国医学研究理事会;
关键词
D O I
10.1002/rmv.551
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human cytomegalovirus (HCMV) is a complex human herpesvirus that is known to productively infect a wide range of cell types. In addition, it has been suggested to contribute to some proliferative disorders, particularly atherosclerosis. Consistent with this, a number of studies have shown that HCMV profoundly affects normal cell cycle control. Specifically, the virus can stimulate early entry into S phase thus ensuring adequate resources for viral DNA replication. Importantly, however, the virus concomitantly inhibits potentially competing cellular DNA synthesis allowing cellular precursors to be used for viral but not cellular DNA replication. The mechanisms by which HCMV perturbs S phase entry involve interactions between the virus and the cellular replication machinery such that formation of competent pre-replication complexes (Pre-RC) at cellular origins of replication is restricted in infected cells. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:423 / 434
页数:12
相关论文
共 100 条
[1]   Structure, expression, and chromosomal localization of the human gene encoding a germinal center-associated nuclear protein (GANP) that associates with MCM3 involved in the initiation of DNA replication [J].
Abe, E ;
Kuwahara, K ;
Yoshida, M ;
Suzuki, M ;
Terasaki, H ;
Matsuo, Y ;
Takahashi, E ;
Sakaguchi, N .
GENE, 2000, 255 (02) :219-227
[2]  
ADAM E, 1987, LANCET, V2, P291
[3]   MALIGNANT TRANSFORMATION OF HAMSTER EMBRYO FIBROBLASTS FOLLOWING EXPOSURE TO ULTRAVIOLET-IRRADIATED HUMAN CYTOMEGALOVIRUS [J].
ALBRECHT, T ;
RAPP, F .
VIROLOGY, 1973, 55 (01) :53-61
[4]   Insights into the mechanisms of CMV-mediated interference with cellular apoptosis [J].
Andoniou, CE ;
Degli-Esposti, MA .
IMMUNOLOGY AND CELL BIOLOGY, 2006, 84 (01) :99-106
[5]   Cell cycle-regulated proteolysis of mitotic target proteins [J].
Bastians, H ;
Topper, LM ;
Gorbsky, GL ;
Ruderman, JV .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (11) :3927-3941
[6]   Human cytomegalovirus infection leads to accumulation of geminin and inhibition of the licensing of cellular DNA replication [J].
Biswas, N ;
Sanchez, V ;
Spector, DH .
JOURNAL OF VIROLOGY, 2003, 77 (04) :2369-2376
[7]   TRANSCRIPTION FACTOR E2F IS REQUIRED FOR EFFICIENT EXPRESSION OF THE HAMSTER DIHYDROFOLATE-REDUCTASE GENE INVITRO AND INVIVO [J].
BLAKE, MC ;
AZIZKHAN, JC .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :4994-5002
[8]  
BOLDOGH I, 1978, ACTA MICROBIOL HUNG, V25, P269
[9]   Retinoblastoma protein recruits histone deacetylase to repress transcription [J].
Brehm, A ;
Miska, EA ;
McCance, DJ ;
Reid, JL ;
Bannister, AJ ;
Kouzarides, T .
NATURE, 1998, 391 (6667) :597-601
[10]   The cyclin E promoter is activated by human cytomegalovirus 86-kDa immediate early protein [J].
Bresnahan, WA ;
Albrecht, T ;
Thompson, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (34) :22075-22082