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Journal of General Virology (2002), 83, 1791-1798.
© 2002 Society for General Microbiology


Plant

Nucleotide sequence shows that Bean leafroll virus has a Luteovirus-like genome organization

Leslie L. Domier1,2, Nancy K. McCoppin1, Richard C. Larsen3 and Cleora J. D’Arcy2

United States Department of Agriculture, Agricultural Research Service1, and Department of Crop Sciences2, 1102 S. Goodwin Ave, University of Illinois at Urbana/Champaign, Urbana, IL 61801, USA
United States Department of Agriculture, Agricultural Research Service, 24106 N Bunn Rd, Prosser, WA 99350-8694, USA3

Author for correspondence: Leslie Domier. Fax +1 217 333 5251. e-mail l-domier{at}uiuc.edu

The complete nucleotide sequence of the Bean leafroll virus (BLRV) genomic RNA and the termini of its smallest subgenomic RNAs were determined to better understand its mechanisms of gene expression and replication and its phylogenetic position within the Luteoviridae. The number and placement of open reading frames (ORFs) within the BLRV genome was Luteovirus-like. The nucleotide and predicted amino acid sequences of BLRV were most similar to those of Soybean dwarf virus (SbDV). Phylogenetic analyses employing the neighbour-joining method and sister-scanning analysis indicated that the BLRV nonstructural proteins were closely related to those of Barley yellow dwarf virus-PAV (BYDV-PAV), a Luteovirus. The region surrounding the frameshift at the junction between ORFs 1 and 2 also contained sequences very similar to those of BYDV-PAV and a Dianthovirus, Red clover necrotic mosaic virus. Similar analyses showed that the structural proteins were most similar to those of the Polerovirus genus. The 3'-noncoding regions downstream of ORF5 contained sequences similar to translational control elements identified in the BYDV-PAV genome. These data suggest that BLRV, like SbDV, is derived either through selection from a common ancestor with BYDV-PAV or that BLRV is the product of two recombination events between luteovirus-like and polerovirus-like ancestors where the 5' 2900 nt and 3' 700 nt of the BLRV genome are from a Luteovirus and the intervening sequences are derived from a Polerovirus.




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R. Shen, A. M. Rakotondrafara, and W. A. Miller
trans Regulation of Cap-Independent Translation by a Viral Subgenomic RNA.
J. Virol., October 1, 2006; 80(20): 10045 - 10054.
[Abstract] [Full Text] [PDF]




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