共 112 条
Parvoviruses: Small Does Not Mean Simple
被引:130
作者:
Cotmore, Susan F.
[1
]
Tattersall, Peter
[1
,2
]
机构:
[1] Yale Univ, Sch Med, Dept Lab Med, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Genet Lab, New Haven, CT 06510 USA
来源:
ANNUAL REVIEW OF VIROLOGY, VOL 1
|
2014年
/
1卷
基金:
美国国家卫生研究院;
关键词:
viral diversity;
limited coding capacity;
dynamic protein cylinder;
capsid portals;
rolling hairpin replication;
early virion release;
ADENOASSOCIATED VIRUS TYPE-2;
NONSTRUCTURAL PROTEINS NS2;
BOCAVIRUS;
INFECTION;
DNA-DAMAGE RESPONSE;
MINK DISEASE VIRUS;
EXPORT FACTOR CRM1;
N-TERMINAL DOMAIN;
CELL-CYCLE ARREST;
LEFT-END HAIRPIN;
MINUTE VIRUS;
D O I:
10.1146/annurev-virology-031413-085444
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Parvoviruses are small, rugged, nonenveloped protein particles containing a linear, nonpermuted, single-stranded DNA genome of similar to 5 kb. Their limited coding potential requires optimal adaptation to the environment of particular host cells, where entry is mediated by a variable program of capsid dynamics, ultimately leading to genome ejection from intact particles within the host nucleus. Genomes are amplified by a continuous unidirectional strand-displacement mechanism, a linear adaptation of rolling circle replication that relies on the repeated folding and unfolding of small hairpin telomeres to reorient the advancing fork. Progeny genomes are propelled by the viral helicase into the preformed capsid via a pore at one of its icosahedral fivefold axes. Here we explore how the fine-tuning of this unique replication system and the mechanics that regulate opening and closing of the capsid fivefold portals have evolved in different viral lineages to create a remarkably complex spectrum of phenotypes.
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页码:517 / +
页数:28
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