2001
DOI: 10.1016/s0168-1702(01)00235-0
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Complete nucleotide sequences of the RNAS 2 of German isolates of Grapevine fanleaf and Arabis mosaic nepoviruses

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Cited by 54 publications
(39 citation statements)
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“…On the other hand, the X1 and VPg of the RNA1, and the 2A of the RNA 2 were the most variable genes on the ArMV genome, confirming previous reports (Wetzel et al, 2001;Ghanem-Sabanadzovic et al, 2005). Interestingly, while only 78% of identity was found between the VPg of ArMV-DU13 and -Lv, 100% identity was found between the VPg of the two ArMV isolates from grapevine (NW and DU13).…”
supporting
confidence: 87%
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“…On the other hand, the X1 and VPg of the RNA1, and the 2A of the RNA 2 were the most variable genes on the ArMV genome, confirming previous reports (Wetzel et al, 2001;Ghanem-Sabanadzovic et al, 2005). Interestingly, while only 78% of identity was found between the VPg of ArMV-DU13 and -Lv, 100% identity was found between the VPg of the two ArMV isolates from grapevine (NW and DU13).…”
supporting
confidence: 87%
“…In addition, in the 5' non-coding region, two nucleotide motifs (5'-GAGUUUAAGAAACUC-3') and (5'-TCCGTTAAGAGCGGA-3'), able to form stemloops structures, were found repeated twice before the insertion. This differed from that observed for the nepoviruses Grapevine deformation virus and Grapevine fanleaf virus (GFLV) (Wetzel et al, 2001;Ghanem-Sabanadzovic et al, 2005), in which only the f irst motif was found repeated three times. The signif icance of these insertions and/or deletions is however unknown.…”
contrasting
confidence: 84%
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“…RNA2 codes for a protein (2A HP ) which is required for RNA2 replication and could act as homing protein [10], the movement protein (2B MP ) which is the constituent protein of tubules observed in plasmodesmata [27], and the coat protein (2C CP ) [32]. The complete RNA 1 (7,342 nt) for strain F13 [27], the RNA2 (3,774 nt) for strain F13 [32] and the German isolates, NW [40] have been sequenced.…”
mentioning
confidence: 99%
“…In PCR reactions, two combinations of primers, 5 0 NC/G0 or 5 0 NC/GMPR1, were used. 5 0 NC (5 0 CCAAGAGTTT(A/G)(A/G)GAAACTCA3 0 ) and G0 (5 0 CAGAATTCCCTTACCCTCTC3 0 ) corresponding to nucleotides (nts) 109-128 and 881-900 of GFLV-F13 [32] were designed by [40] as the forward and reverse primers, respectively. Amplification by these primers was expected to produce a 792 bp fragment encompassing 126 nts of 5 0 UTR and 668 nts of 5 0 proximity of 2A HP gene located on the virus RNA2 segment.…”
mentioning
confidence: 99%