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The human polyoma JC virus agnoprotein acts as a viroporin
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نویسنده
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suzuki t. ,orba y. ,okada y. ,sunden y. ,kimura t. ,tanaka s. ,nagashima k. ,hall w.w. ,sawa h.
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منبع
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plos pathogens - 2010 - دوره : 6 - شماره : 3
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چکیده
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Virus infections can result in a range of cellular injuries and commonly this involves both the plasma and intracellular membranes,resulting in enhanced permeability. viroporins are a group of proteins that interact with plasma membranes modifying permeability and can promote the release of viral particles. while these proteins are not essential for virus replication,their activity certainly promotes virus growth. progressive multifocal leukoencephalopathy (pml) is a fatal demyelinating disease resulting from lytic infection of oligodendrocytes by the polyomavirus jc virus (jcv). the genome of jcv encodes six major proteins including a small auxiliary protein known as agnoprotein. studies on other polyomavirus agnoproteins have suggested that the protein may contribute to viral propagation at various stages in the replication cycle,including transcription,translation,processing of late viral proteins,assembly of virions,and viral propagation. previous studies from our and other laboratories have indicated that jcv agnoprotein plays an important,although as yet incompletely understood role in the propagation of jcv. here,we demonstrate that agnoprotein possesses properties commonly associated with viroporins. our findings demonstrate that: (i) a deletion mutant of agnoprotein is defective in virion release and viral propagation; (ii) agnoprotein localizes to the er early in infection,but is also found at the plasma membrane late in infection; (iii) agnoprotein is an integral membrane protein and forms homo-oligomers; (iv) agnoprotein enhances permeability of cells to the translation inhibitor hygromycin b; (v) agnoprotein induces the influx of extracellular ca2+; (vi) the basic residues at amino acid positions 8 and 9 of agnoprotein key are determinants of the viroporin activity. the viroporin-like properties of agnoprotein result in increased membrane permeability and alterations in intracellular ca2+ homeostasis leading to membrane dysfunction and enhancement of virus release. © 2010 suzuki et al.
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آدرس
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department of molecular pathobiology,hokkaido university research center for zoonosis control,sapporo,japan,department of pathology,national institute of infectious diseases,musashimurayama,tokyo, Japan, department of molecular pathobiology,hokkaido university research center for zoonosis control,sapporo,japan,global coe program for zoonosis control,hokkaido university,sapporo, Japan, career-path promotion unit for young life scientists,icdo,kyoto university,kyoto, Japan, laboratory of comparative pathology,hokkaido university school of veterinary medicine,sapporo, Japan, department of molecular pathobiology,hokkaido university research center for zoonosis control,sapporo, Japan, laboratory of cancer research,department of pathology,hokkaido university school of medicine,sapporo, Japan, laboratory of cancer research,department of pathology,hokkaido university school of medicine,sapporo, Japan, centre for research in infectious diseases,university college dublin,dublin, Ireland, department of molecular pathobiology,hokkaido university research center for zoonosis control,sapporo,japan,global coe program for zoonosis control,hokkaido university,sapporo, Japan
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Authors
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