Accumulation of specific RNAs encoding transcriptional factors and stress response proteins against a background of severe depletion of cellular RNAs in cells infected with herpes simplex virus 1

被引:51
作者
Khodarev, NN
Advani, SJ
Gupta, N
Roizman, B
Weichselbaum, RR
机构
[1] Univ Chicago, Dept Radiat & Cellular Oncol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Surg, Chicago, IL 60637 USA
[3] Univ Chicago, Marjorie B Kovler Viral Oncol Labs, Chicago, IL 60637 USA
关键词
D O I
10.1073/pnas.96.21.12062
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
Herpes simplex virus 1 encodes several functions to preclude the shutoff of host response to infection, including degradation of mRNA immediately after infection. To determine whether any cellular mRNAs accumulate in infected cells against a background of severe loss of host RNA, we hybridized cDNAs derived from three different cell lines infected with wild type and a mutant virus to a DNA array containing probes for 588 human genes representing different functional groups. The results were that (i) infected cells accumulated at levels above those of mock-infected cells, a small number of transcripts representing transcriptional factors that could regulate gene expression both positively and negatively, and one stress response protein (GADD45), (ii) the amount and nature of the accumulated transcripts showed limited variability depending on the cell and virus, and (iii) at least some of the proteins encoded by the accumulated transcripts could benefit either the virus or the host.
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页码:12062 / 12067
页数:6
相关论文
共 45 条
[1]   THE PROTEIN ID - A NEGATIVE REGULATOR OF HELIX-LOOP-HELIX DNA-BINDING PROTEINS [J].
BENEZRA, R ;
DAVIS, RL ;
LOCKSHON, D ;
TURNER, DL ;
WEINTRAUB, H .
CELL, 1990, 61 (01) :49-59
[2]  
CAO XM, 1993, J BIOL CHEM, V268, P16949
[3]   Feedback inhibition of macrophage tumor necrosis factor-α production by tristetraprolin [J].
Carballo, E ;
Lai, WS ;
Blackshear, PJ .
SCIENCE, 1998, 281 (5379) :1001-1005
[4]   MAPPING OF HERPES-SIMPLEX VIRUS-1 NEUROVIRULENCE TO GAMMA-134.5, A GENE NONESSENTIAL FOR GROWTH IN CULTURE [J].
CHOU, J ;
KERN, ER ;
WHITLEY, RJ ;
ROIZMAN, B .
SCIENCE, 1990, 250 (4985) :1262-1266
[5]   ASSOCIATION OF A M(R)-90,000 PHOSPHOPROTEIN WITH PROTEIN-KINASE PKR IN CELLS EXHIBITING ENHANCED PHOSPHORYLATION OF TRANSLATION INITIATION-FACTOR EIF-2-ALPHA AND PREMATURE SHUTOFF OF PROTEIN-SYNTHESIS AFTER INFECTION WITH GAMMA(1)34.5(-) MUTANTS OF HERPES-SIMPLEX-VIRUS-1 [J].
CHOU, J ;
CHEN, JJ ;
GROSS, M ;
ROIZMAN, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (23) :10516-10520
[6]   AN ID-RELATED HELIX LOOP HELIX PROTEIN ENCODED BY A GROWTH FACTOR-INDUCIBLE GENE [J].
CHRISTY, BA ;
SANDERS, LK ;
LAU, LF ;
COPELAND, NG ;
JENKINS, NA ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (05) :1815-1819
[7]   Regulation of Id3 cell cycle function by Cdk-2-dependent phosphorylation [J].
Deed, RW ;
Hara, E ;
Atherton, GT ;
Peters, G ;
Norton, JD .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (12) :6815-6821
[8]   MAMMALIAN GENES COORDINATELY REGULATED BY GROWTH ARREST SIGNALS AND DNA-DAMAGING AGENTS [J].
FORNACE, AJ ;
NEBERT, DW ;
HOLLANDER, MC ;
LUETHY, JD ;
PAPATHANASIOU, M ;
FARGNOLI, J ;
HOLBROOK, NJ .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (10) :4196-4203
[9]   Herpes simplex virus 1 blocks caspase-3-independent and caspase-dependent pathways to cell death [J].
Galvan, V ;
Brandimarti, R ;
Roizman, B .
JOURNAL OF VIROLOGY, 1999, 73 (04) :3219-3226
[10]   Herpes simplex virus 1 induces and blocks apoptosis at multiple steps during infection and protects cells from exogenous inducers in a cell-type-dependent manner [J].
Galvan, V ;
Roizman, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3931-3936