Components of Adenovirus Genome Packaging

被引:59
作者
Ahi, Yadvinder S. [1 ,2 ]
Mittal, Suresh K. [1 ,2 ,3 ]
机构
[1] Purdue Univ, Dept Comparat Pathobiol, W Lafayette, IN 47907 USA
[2] Purdue Univ, Ctr Canc Res, W Lafayette, IN 47907 USA
[3] Purdue Univ, Purdue Inst Immunol Inflammat & Infect Dis, W Lafayette, IN 47907 USA
来源
FRONTIERS IN MICROBIOLOGY | 2016年 / 7卷
关键词
adenovirus; genome packaging; IVa2; L4; 33K; 22K; ATPase; packaging domain; portal vertex; DNA-BINDING PROTEIN; TEMPERATURE-SENSITIVE MUTANT; IVA2; GENE-PRODUCT; L1 52/55-KILODALTON PROTEIN; MAJOR CAPSID PROTEIN; VIRAL-DNA; INCOMPLETE PARTICLES; IN-VITRO; 33K PROTEIN; SUBGROUP-C;
D O I
10.3389/fmicb.2016.01503
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adenoviruses (AdVs) are icosahedral viruses with double-stranded DNA (dsDNA) genomes. Genome packaging in AdV is thought to be similar to that seen in dsDNA containing icosahedral bacteriophages and herpesviruses. Specific recognition of the AdV genome is mediated by a packaging domain located close to the left end of the viral genome and is mediated by the viral packaging machinery. Our understanding of the role of various components of the viral packaging machinery in AdV genome packaging has greatly advanced in recent years. Characterization of empty capsids assembled in the absence of one or more components involved in packaging, identification of the unique vertex, and demonstration of the role of IVa2, the putative packaging ATPase, in genome packaging have provided compelling evidence that AdVs follow a sequential assembly pathway. This review provides a detailed discussion on the functions of the various viral and cellular factors involved in AdV genome packaging. We conclude by briefly discussing the roles of the empty capsids, assembly intermediates, scaffolding proteins, portal vertex and DNA encapsidating enzymes in AdV assembly and packaging.
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页数:15
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共 128 条
  • [1] Adenoviral L4 33K forms ring-like oligomers and stimulates ATPase activity of IVa2: implications in viral genome packaging
    Ahi, Yadvinder S.
    Vemula, Sai V.
    Hassan, Ahmed O.
    Costakes, Greg
    Stauffacher, Cynthia
    Mittal, Suresh K.
    [J]. FRONTIERS IN MICROBIOLOGY, 2015, 6
  • [2] Adenoviral E2 IVa2 protein interacts with L4 33K protein and E2 DNA-binding protein
    Ahi, Yadvinder S.
    Vemula, Sai V.
    Mittal, Suresh K.
    [J]. JOURNAL OF GENERAL VIROLOGY, 2013, 94 : 1325 - 1334
  • [3] The adenovirus L4 33-kilodalton protein binds to intragenic sequences of the major late promoter required for late phase-specific stimulation of transcription
    Ali, Humayra
    Leroy, Gary
    Bridge, Gernma
    Flint, S. J.
    [J]. JOURNAL OF VIROLOGY, 2007, 81 (03) : 1327 - 1338
  • [4] Granzyme H destroys the function of critical adenoviral proteins required for viral DNA replication and granzyme B inhibition
    Andrade, Felipe
    Fellows, Edward
    Jenne, Dieter E.
    Rosen, Antony
    Young, C. S. H.
    [J]. EMBO JOURNAL, 2007, 26 (08) : 2148 - 2157
  • [5] CLEAVAGE PRODUCT OF THE ADENOVIRUS DNA-BINDING PROTEIN IS ACTIVE IN DNA-REPLICATION INVITRO
    ARIGA, H
    KLEIN, H
    LEVINE, AJ
    HORWITZ, MS
    [J]. VIROLOGY, 1980, 101 (01) : 307 - 310
  • [6] Adenovirus Composition, Proteolysis, and Disassembly Studied by In-depth Qualitative and Quantitative Proteomics
    Benevento, Marco
    Di Palma, Serena
    Snijder, Joost
    Moyer, Crystal L.
    Reddy, Vijay S.
    Nemerow, Glen R.
    Heck, Albert J. R.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (16) : 11421 - 11430
  • [7] Does common architecture reveal a viral lineage spanning all three domains of life?
    Benson, SD
    Bamford, JKH
    Bamford, DH
    Burnett, RM
    [J]. MOLECULAR CELL, 2004, 16 (05) : 673 - 685
  • [8] ACCUMULATION OF EARLY AND INTERMEDIATE MESSENGER-RNA SPECIES DURING SUBGROUP-C ADENOVIRUS PRODUCTIVE INFECTIONS
    BINGER, MH
    FLINT, SJ
    [J]. VIROLOGY, 1984, 136 (02) : 387 - 403
  • [9] TRANSFORMATION OF SENSORY ORGANS BY MUTATIONS OF THE CUT LOCUS OF DROSOPHILA-MELANOGASTER
    BODMER, R
    BARBEL, S
    SHEPERD, S
    JACK, JW
    JAN, LY
    JAN, YN
    [J]. CELL, 1987, 51 (02) : 293 - 307
  • [10] DIFFERENT BINDING-SITE REQUIREMENTS FOR BINDING AND ACTIVATION FOR THE BIPARTITE ENHANCER FACTOR EF-1A
    BOLWIG, GM
    BRUDER, JT
    HEARING, P
    [J]. NUCLEIC ACIDS RESEARCH, 1992, 20 (24) : 6555 - 6564