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J Gen Virol 72 (1991), 2325-2331; DOI 10.1099/0022-1317-72-10-2325
© 1991 Society for General Microbiology

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The nucleotide sequence and genome structure of the geminivirus miscanthus streak virus

Masaaki Chatani1,3, Yoshinori Matsumoto1, Haruyoshi Mizuta1,3, Masato Ikegami2, Margaret I. Boulton3 and Jeffrey W. Davies3

1 Nippon Oil Company Ltd, 766 Higashitoyoi, Kudamatsu-shi, Yamaguchi 744
2 Nodai Research Institute, Tokyo University of Agriculture, 1-1 Sakuragaoka, Setagaya-ku, Tokyo 156, Japan
and3 John Innes Institute, John Innes Centre for Plant Science Research, Colney Lane, Norwich NR4 7UH, U.K.

A tandem dimer of miscanthus streak virus (MiSV) DNA was inserted into the T-DNA of the binary plasmid vector pBIN19 and agroinoculated into several monocotyledonous plants (monocots) using Agrobacterium tumefaciens or A. rhizogenes. Disease symptoms and geminate particles were produced in maize and Panicum milaceum plants, and MiSV-specific double-stranded and single-stranded DNAs were found in these plants. The nucleotide sequence of the infectious MiSV clone, consisting of 2672 nucleotides, was determined. Four open reading frames (ORFs) for proteins of Mr greater than 10K were identified, two (V0 and V2) in the virus (+) sense and two (C1 and C2) in the complementary (-) sense, although C2 did not have an ATG start codon. Unlike other geminiviruses infecting monocots, complementary-sense ORFs did not overlap. Potential splicing donor and acceptor sites were identified in the sequence of the border region between the C terminus of ORF C1 and the N terminus of ORF C2. Amino acid sequences predicted from three (V2, C1 and C2) of these ORFs showed significant homology with the corresponding ORFs of other geminiviruses infecting monocots. A fifth ORF (V1), which showed some homology with ORF V1 of other monocot-infecting geminiviruses despite having a coding capacity for a product of Mr 8.8K, was found just upstream of ORF V2 as observed in those geminiviruses. ORF V0 showed no significant homology with ORFs present in any other geminiviruses. A mutation of V0 indicated that the C-terminal 30% of this ORF was not necessary for infection in maize, but that sequences around the mutated LspI site might have some regulatory role.

Received 18 February 1991; accepted 10 June 1991.





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Copyright © 1991 by the Society for General Microbiology.