Translational control of viral gene expression in eukaryotes

被引:266
作者
Gale, M
Tan, SL
Katze, MG
机构
[1] Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA
[2] Univ Washington, Seattle, WA 98195 USA
关键词
D O I
10.1128/MMBR.64.2.239-280.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
As obligate intracellular parasites, viruses rely exclusively on the translational machinery of the host cell for the synthesis of viral proteins. This relationship has imposed numerous challenges on both the infecting virus and the host cell. Importantly, viruses must compete with the endogenous transcripts of the host cell for the translation of viral mRNA. Eukaryotic viruses have thus evolved diverse mechanisms to ensure translational efficiency of viral mRNA above and beyond that of cellular mRNA. Mechanisms that facilitate the efficient and selective translation of viral mRNA may be inherent in the structure of the viral nucleic acid itself and can involve the recruitment and/or modification of specific host factors. These processes serve to redirect the translation apparatus to favor viral transcripts and they often come at the expense of the host cell. Accordingly, eukaryotic cells have developed antiviral countermeasures to target the translational machinery and disrupt protein synthesis during the course of virus infection. Not to be outdone many viruses have answered these countermeasures with their own mechanisms to disrupt cellular antiviral pathways, thereby ensuring the uncompromised translation of virion proteins Here we review the varied and complex translational programs employed by eukaryotic viruses. We discuss how these translational strategies have been incorporated into the virus life cycle and examine how such programming contributes to the pathogenesis of the host cell.
引用
收藏
页码:239 / +
页数:43
相关论文
共 502 条
  • [1] Agol VI, 1998, MOL BIOL+, V32, P44
  • [2] Antisense oligonucleotides as therapeutic agents
    Alama, A
    Barbieri, F
    Cagnoli, M
    Schettini, G
    [J]. PHARMACOLOGICAL RESEARCH, 1997, 36 (03) : 171 - 178
  • [3] INTERACTION OF POLYPYRIMIDINE TRACT-BINDING PROTEIN WITH THE 5'-NONCODING REGION OF THE HEPATITIS-C VIRUS-RNA GENOME AND ITS FUNCTIONAL REQUIREMENT IN INTERNAL INITIATION OF TRANSLATION
    ALI, N
    SIDDIQUI, A
    [J]. JOURNAL OF VIROLOGY, 1995, 69 (10) : 6367 - 6375
  • [4] Ali N, 1995, Princess Takamatsu Symp, V25, P99
  • [5] EFFICIENT TRANSCRIPTION, NOT TRANSLATION, IS DEPENDENT ON ADENOVIRUS TRIPARTITE LEADER SEQUENCES AT LATE TIMES OF INFECTION
    ALONSOCAPLEN, FV
    KATZE, MG
    KRUG, RM
    [J]. JOURNAL OF VIROLOGY, 1988, 62 (05) : 1606 - 1616
  • [6] Epidemiology of hepatitis C
    Alter, MJ
    [J]. HEPATOLOGY, 1997, 26 (03) : S62 - S65
  • [7] Correlation between virus genotype and chronicity rate in acute hepatitis C
    Amoroso, P
    Rapicetta, M
    Tosti, ME
    Mele, A
    Spada, E
    Buonocore, S
    Lettieri, G
    Pierri, P
    Chionne, P
    Ciccaglione, AR
    Sagliocca, L
    [J]. JOURNAL OF HEPATOLOGY, 1998, 28 (06) : 939 - 944
  • [8] Andreansky S, 1997, CANCER RES, V57, P1502
  • [9] [Anonymous], 1990, Virology
  • [10] Virus-induced host gene shutoff in animals and plants
    Aranda, M
    Maule, A
    [J]. VIROLOGY, 1998, 243 (02) : 261 - 267