Identification of the genome-linked protein in virions of Potato virus A, with comparison to other members in genus Potyvirus

被引:39
作者
Oruetxebarria, I
Guo, DY
Merits, A
Mäkinen, K
Saarma, M
Valkonen, JPT
机构
[1] SLU, Dept Plant Biol, Genet Ctr, S-75007 Uppsala, Sweden
[2] Univ Helsinki, Vikki Bioctr, Inst Biotechnol, FIN-00014 Helsinki, Finland
关键词
Potato virus A; Potyvirus; tobacco vein mottling virus;
D O I
10.1016/S0168-1702(00)00216-1
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Viruses of the genus Potyvirus. the largest genus of plant-infecting viruses, have a messenger-polarity ssRNA genome encapsidated by approximately 2000 units of the viral coat protein (CP), resulting in filamentous virions. Only few studies have examined potyvirus virions for the presence of other structural proteins. A protein linked covalently to the 5'-end of the genome has been identified in Tobacco vein mottling virus (TVMV) and Tobacco etch virus (TEV). In TEV, it is either the viral NIa protein or only its N-terminal domain (VPg) separated autocatalytically From the C-terminal proteinase domain (NIa-Pro). Virions of TVMV carry only the VPg. We examined virions of Potato virus A (PVA) for the genome-linked protein using immunoblotting or iodination and immunoprecipitation. The VPg ( similar to 25 kDa) only, and not the unprocessed NIa, was detected. Another signal corresponding to similar to 49 kDa was detected in disrupted, RNase-treated virions with anti-VPg antibodies but not with antibodies to NIa-Pro. Since it possibly represented a dimeric form of the VPg, self-interaction of the VPg was tested using the yeast two-hybrid system, which showed that the VPg self-interacts in the absence of viral RNA. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
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页码:103 / 112
页数:10
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