The Red clover necrotic mosaic virus origin of assembly is delimited to the RNA-2 trans-activator

被引:28
作者
Basnayake, Veronica R. [1 ]
Sit, Tim L. [1 ]
Lommel, Steven A. [1 ]
机构
[1] N Carolina State Univ, Dept Plant Pathol, Plant Virol Grp, Raleigh, NC 27695 USA
关键词
Red clover necrotic mosaic virus; Virion assembly; Origin of assembly; trans-activator; Dianthovirus; Tombusviridae; TURNIP CRINKLE VIRUS; DIRECTED MUTAGENESIS; NUCLEOTIDE-SEQUENCE; BARLEY PROTOPLASTS; PACKAGING SIGNAL; SUBGENOMIC RNA; TYPE-1; GENOME; PLANT-VIRUS; IN-VITRO; ENCAPSIDATION;
D O I
10.1016/j.virol.2008.11.005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The bipartite RNA genome of Red clover necrotic mosaic virus (RCNMV) is encapsidated into icosahedral virions that exist as two populations: i) virions that co-package both genomic RNAs and ii) virions packaging multiple copies of RNA-2. To elucidate the packaging mechanism, we sought to identify the RCNMV origin of assembly sequence (OAS). RCNMV RNA-1 cannot package in the absence of RNA-2 suggesting that it does not contain an independent packaging signal. A 209 nt RNA-2 element expressed from the Tomato bushy stunt virus CP subgenomic promoter is co-assembled with genomic RNA-1 into virions. Deletion mutagenesis delimited the previously characterized 34 nt trans-activator (TA) as the minimal RCNMV OAS. From this study we hypothesize that RNA-1 must be base-paired with RNA-2 at the TA to initiate co-packaging. The addition of viral assembly illustrates the critical importance of the multifunctional TA element as a key regulatory switch in the RCNMV life cycle. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:169 / 178
页数:10
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