חיפוש מתקדם
Phytopathologia Mediterranea
Rosner, A., Virology Department, ARO, The Volcani Center, Bet Dagan 50250, Israel
Maslenin, L., Virology Department, ARO, The Volcani Center, Bet Dagan 50250, Israel
Potato isolates of Potato virus Y (PVY) were divided into two major groups based on nucleotide sequence homology in the 5'-end region of their genomes. Several characteristic nucleotide modifications differentiated the two virus groups. Sequence similarity within members of each group was 89-100%, whereas between members of the respective groups there was sequence divergence of up to 33%. The two groups were distinguished by restriction cleavage of the virus PCR products elicited by group-specific restriction endonucleases: Xho II and Nsp I (group I) and Mbo II, Fok I and Nco I (group II). The sites of the first three enzymes (group I-specific) were sequentially positioned so that a sequence of 16 nucleotides preceding the ATG codon could be determined in this way. Group I included members of the tobacco necrotic (N) and non-necrotic (O) strains of PVY, whereas the potato tuber necrotic isolate NTN-H belonged to the second group, which included also non-tuber and tobacco leaf necrotic members. It seems therefore that the biological characteristics of the tuber or tobacco leaf necrosis are not related to nucleotide modifications at the 5'-UTR but rather to group-specific differences.
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תנאי שימוש
Grouping of potato isolates of PVY based on the 5'-UTR nucleotide sequence
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Rosner, A., Virology Department, ARO, The Volcani Center, Bet Dagan 50250, Israel
Maslenin, L., Virology Department, ARO, The Volcani Center, Bet Dagan 50250, Israel
Grouping of potato isolates of PVY based on the 5'-UTR nucleotide sequence
Potato isolates of Potato virus Y (PVY) were divided into two major groups based on nucleotide sequence homology in the 5'-end region of their genomes. Several characteristic nucleotide modifications differentiated the two virus groups. Sequence similarity within members of each group was 89-100%, whereas between members of the respective groups there was sequence divergence of up to 33%. The two groups were distinguished by restriction cleavage of the virus PCR products elicited by group-specific restriction endonucleases: Xho II and Nsp I (group I) and Mbo II, Fok I and Nco I (group II). The sites of the first three enzymes (group I-specific) were sequentially positioned so that a sequence of 16 nucleotides preceding the ATG codon could be determined in this way. Group I included members of the tobacco necrotic (N) and non-necrotic (O) strains of PVY, whereas the potato tuber necrotic isolate NTN-H belonged to the second group, which included also non-tuber and tobacco leaf necrotic members. It seems therefore that the biological characteristics of the tuber or tobacco leaf necrosis are not related to nucleotide modifications at the 5'-UTR but rather to group-specific differences.
Scientific Publication
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