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Molecular cloning and complete nucleotide sequence of carnation Italian ringspot tombusvirus genomic and defective interfering RNAs
Authors:L. Rubino  J. Burgyan  M. Russo
Affiliation:(1) Dipartimento di Protezione delle Piante, Università degli Studi, Bari, Italy;(2) Centro di Studio del CNR sui Virus e le Virosi delle Colture Mediterranee, Bari, Italy;(3) Present address: Agricultural Biotechnology Center, H-2101 Gödöllo, Hungary
Abstract:Summary The complete sequences of genomic and defective interfering (DI) RNAs of carnation Italian ringspot tombusvirus (CIRV) were determined. The genome (4760 nt) has an organization identical to that reported for other tombusviruses except that the pre-readthrough domain of the viral replicase encoded by the 5prime-proximal open reading frame (ORF) is larger. In particular, the N-terminal region of this protein differs from the corresponding region of the other members of the genusTombusvirus andCarmovirus. Two DI RNAs were found in infected tissues whose sequences were completely derived from genomic RNA. The smaller molecule (474 nt) is contained completely within the larger molecule (656 nt), which suggests that it is derived from the larger one.The nucleotide sequence data reported in this paper will appear in the EMBL, GenBank and DDBJ Nucleotide Database under the accession number X85215.
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