The human cytomegalovirus UL82 gene product (pp71) accelerates progression through the G1 phase of the cell cycle

被引:50
作者
Kalejta, RF [1 ]
Shenk, T [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
关键词
D O I
10.1128/JVI.77.6.3451-3459.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
As viruses are reliant upon their host cell to serve as proper environments for their replication, many have evolved mechanisms to alter intracellular conditions to suit their own needs. For example, human cytomegalovirus induces quiescent cells to enter the cell cycle and then arrests them in late G(1), before they enter the S phase, a cell cycle compartment that is presumably favorable for viral replication. Here we show that the protein product of the human cytomegalovirus UL82 gene, pp71, can accelerate the movement of cells through the G(1) phase of the cell cycle. This activity would help infected cells reach the late G(1) arrest point sooner and thus may stimulate the infectious cycle. pp71 also induces DNA synthesis in quiescent cells, but a pp71 mutant protein that is unable to induce quiescent cells to enter the cell cycle still retains the ability to accelerate the G(1) phase. Thus, the mechanism through which pp71 accelerates G(1) cell cycle progression appears to be distinct from the one that it employs to induce quiescent cells to exit G(0) and subsequently enter the S phase.
引用
收藏
页码:3451 / 3459
页数:9
相关论文
共 83 条
[1]   REGULATION OF G(1)/S TRANSITION BY CYCLIN-D2 AND CYCLIN-D3 IN HEMATOPOIETIC-CELLS [J].
ANDO, K ;
AJCHENBAUMCYMBALISTA, F ;
GRIFFIN, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (20) :9571-9575
[2]   Human cytomegalovirus tegument protein pp71 (ppUL82) enhances the infectivity of viral DNA and accelerates the infectious cycle [J].
Baldick, CJ ;
Marchini, A ;
Patterson, CE ;
Shenk, T .
JOURNAL OF VIROLOGY, 1997, 71 (06) :4400-4408
[3]   THE ORNITHINE DECARBOXYLASE GENE IS A TRANSCRIPTIONAL TARGET OF C-MYC [J].
BELLOFERNANDEZ, C ;
PACKHAM, G ;
CLEVELAND, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) :7804-7808
[4]   ACTIVATION OF PROTO-ONCOGENES - AN IMMEDIATE EARLY EVENT IN HUMAN CYTOMEGALOVIRUS-INFECTION [J].
BOLDOGH, I ;
ABUBAKAR, S ;
ALBRECHT, T .
SCIENCE, 1990, 247 (4942) :561-564
[5]   Human cytomegalovirus inhibits cellular DNA synthesis and arrests productively infected cells in late G1 [J].
Bresnahan, WA ;
Boldogh, I ;
Thompson, EA ;
Albrecht, T .
VIROLOGY, 1996, 224 (01) :150-160
[6]   UL82 virion protein activates expression of immediate early viral genes in human cytomegalovirus-infected cells [J].
Bresnahan, WA ;
Shenk, TE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) :14506-14511
[7]   The Us9 gene product of pseudorabies virus, an alphaherpesvirus, is a phosphorylated, tail-anchored type II membrane protein [J].
Brideau, AD ;
Banfield, BW ;
Enquist, LW .
JOURNAL OF VIROLOGY, 1998, 72 (06) :4560-4570
[8]   Altered cellular mRNA levels in human cytomegalovirus-infected fibroblasts: Viral block to the accumulation of antiviral mRNAs [J].
Browne, EP ;
Wing, B ;
Coleman, D ;
Shenk, T .
JOURNAL OF VIROLOGY, 2001, 75 (24) :12319-12330
[9]   Role of human cytomegalovirus immediate-early proteins in cell growth control [J].
Castillo, JP ;
Yurochko, AD ;
Kowalik, TF .
JOURNAL OF VIROLOGY, 2000, 74 (17) :8028-8037
[10]   Human cytomegalovirus immediate early proteins and cell growth control [J].
Castillo, JP ;
Kowalik, TF .
GENE, 2002, 290 (1-2) :19-34