Viral subversion of nucleocytoplasmic trafficking.
Identifieur interne : 001533 ( Main/Exploration ); précédent : 001532; suivant : 001534Viral subversion of nucleocytoplasmic trafficking.
Auteurs : Melanie L. Yarbrough [États-Unis] ; Miguel A. Mata ; Ramanavelan Sakthivel ; Beatriz M A. FontouraSource :
- Traffic (Copenhagen, Denmark) [ 1600-0854 ] ; 2014.
Descripteurs français
- KwdFr :
- MESH :
- métabolisme : Cytoplasme, Noyau de la cellule, Virus.
- pathogénicité : Virus.
- virologie : Cytoplasme, Noyau de la cellule.
- Animaux, Humains, Transport des ARN, Transport nucléaire actif.
English descriptors
- KwdEn :
- MESH :
- metabolism : Cell Nucleus, Cytoplasm, Viruses.
- pathogenicity : Viruses.
- virology : Cell Nucleus, Cytoplasm.
- Active Transport, Cell Nucleus, Animals, Humans, RNA Transport.
Abstract
Trafficking of proteins and RNA into and out of the nucleus occurs through the nuclear pore complex (NPC). Because of its critical function in many cellular processes, the NPC and transport factors are common targets of several viruses that disrupt key constituents of the machinery to facilitate viral replication. Many viruses such as poliovirus and severe acute respiratory syndrome (SARS) virus inhibit protein import into the nucleus, whereas viruses such as influenza A virus target and disrupt host mRNA nuclear export. Current evidence indicates that these viruses may employ such strategies to avert the host immune response. Conversely, many viruses co-opt nucleocytoplasmic trafficking to facilitate transport of viral RNAs. As viral proteins interact with key regulators of the host nuclear transport machinery, viruses have served as invaluable tools of discovery that led to the identification of novel constituents of nuclear transport pathways. This review explores the importance of nucleocytoplasmic trafficking to viral pathogenesis as these studies revealed new antiviral therapeutic strategies and exposed previously unknown cellular mechanisms. Further understanding of nuclear transport pathways will determine whether such therapeutics will be useful treatments for important human pathogens.
DOI: 10.1111/tra.12137
PubMed: 24289861
Affiliations:
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Le document en format XML
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<term>Cytoplasm (metabolism)</term>
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<term>Humans</term>
<term>RNA Transport</term>
<term>Viruses (metabolism)</term>
<term>Viruses (pathogenicity)</term>
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<term>Cytoplasme (virologie)</term>
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<term>Noyau de la cellule (métabolisme)</term>
<term>Noyau de la cellule (virologie)</term>
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<term>Transport nucléaire actif</term>
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<term>Virus (pathogénicité)</term>
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<term>Cytoplasm</term>
<term>Viruses</term>
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<front><div type="abstract" xml:lang="en">Trafficking of proteins and RNA into and out of the nucleus occurs through the nuclear pore complex (NPC). Because of its critical function in many cellular processes, the NPC and transport factors are common targets of several viruses that disrupt key constituents of the machinery to facilitate viral replication. Many viruses such as poliovirus and severe acute respiratory syndrome (SARS) virus inhibit protein import into the nucleus, whereas viruses such as influenza A virus target and disrupt host mRNA nuclear export. Current evidence indicates that these viruses may employ such strategies to avert the host immune response. Conversely, many viruses co-opt nucleocytoplasmic trafficking to facilitate transport of viral RNAs. As viral proteins interact with key regulators of the host nuclear transport machinery, viruses have served as invaluable tools of discovery that led to the identification of novel constituents of nuclear transport pathways. This review explores the importance of nucleocytoplasmic trafficking to viral pathogenesis as these studies revealed new antiviral therapeutic strategies and exposed previously unknown cellular mechanisms. Further understanding of nuclear transport pathways will determine whether such therapeutics will be useful treatments for important human pathogens. </div>
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<name sortKey="Sakthivel, Ramanavelan" sort="Sakthivel, Ramanavelan" uniqKey="Sakthivel R" first="Ramanavelan" last="Sakthivel">Ramanavelan Sakthivel</name>
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