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Cellular versus viral microRNAs in host-virus interaction
被引:155
作者:
Ghosh, Zhumur
[1
]
Mallick, Bibekanand
[1
]
Chakrabarti, Jayprokas
[1
,2
]
机构:
[1] Indian Assoc Cultivat Sci, Computat Biol Grp, Kolkata 700032, W Bengal, India
[2] Gyanxet, Kolkata 700064, W Bengal, India
关键词:
ENCODED MICRORNAS;
GENE-EXPRESSION;
PROTEIN-SYNTHESIS;
TARGET GENES;
RNA;
IDENTIFICATION;
INFECTION;
LATENCY;
HIV-1;
MODULATION;
D O I:
10.1093/nar/gkn1004
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
MicroRNAs (miRNAs) mark a new paradigm of RNA-directed gene expression regulation in a wide spectrum of biological systems. These small non-coding RNAs can contribute to the repertoire of host-pathogen interactions during viral infection. This interplay has important consequences, both for the virus and the host. There have been reported evidences of host-cellular miRNAs modulating the expression of various viral genes, thereby playing a pivotal role in the host-pathogen interaction network. In the hide-and-seek game between the pathogens and the infected host, viruses have evolved highly sophisticated gene-silencing mechanisms to evade host-immune response. Recent reports indicate that virus too encode miRNAs that protect them against cellular antiviral response. Furthermore, they may exploit the cellular miRNA pathway to their own advantage. Nevertheless, our increasing knowledge of the host-virus interaction at the molecular level should lead us toward possible explanations to viral tropism, latency and oncogenesis along with the development of an effective, durable and nontoxic antiviral therapy. Here, we summarize the recent updates on miRNA-induced gene-silencing mechanism, modulating host-virus interactions with a glimpse of the miRNA-based antiviral therapy for near future.
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页码:1035 / 1048
页数:14
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