Skip Navigation

This Article
Right arrow Print PDF (574K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (105)
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Visvader, J. E.
Right arrow Articles by Symons, R. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Visvader, J. E.
Right arrow Articles by Symons, R. H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1985, Vol. 13, No. 8 2907-2920
© 1985


Articles

Eleven new sequence variants of citrus exocortis viroid and the correlation of sequence with pathogenicity

Jane E. Visvader and Robert H. Symons

Adelaide University Centre for Gene Technology, Department of Biochemistry, University of Adelaide Adelaide, South Australia 5000, Australia

Received March 4, 1985. Accepted March 22, 1985.

Full-length double-stranded cDNA was prepared from purified circular RNA of two new Australian field isolates of citrus exocortis viroid (CEV) using two synthetic oligodeoxynucleotide primers. The cDNA was then cloned into the phage vector M13mp9 for sequence analysis. Sequencing of nine cDNA clones of isolate CEV-DE30 and eleven cDNA clones of isolate CEV-J indicated that both isolates consisted of a mixture of viroid species and led to the discovery of eleven new sequence variants of CEV. These new variants, together with the six reported previously, form two classes of sequence which differ by a minimum of 26 nucleotides in a total of 370 to 315 residues. These two classes correlate with two biologically distinct groups when propagated on tomato plants where one produces severe symptoms and the other gives rise to mild symptoms. Two regions of the native structure of CEV, comprising 18% of the total residues, differ between the sequence variants of mild and severe isolates. Whether or not both of these regions are essential for the variation in pathogenicity has yet to be determined.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Virol.Home page
X. Zhong, N. Leontis, S. Qian, A. Itaya, Y. Qi, K. Boris-Lawrie, and B. Ding
Tertiary structural and functional analyses of a viroid RNA motif by isostericity matrix and mutagenesis reveal its essential role in replication.
J. Virol., September 1, 2006; 80(17): 8566 - 8581.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
R. P. Singh, X. Nie, and M. Singh
Tomato chlorotic dwarf viroid: an evolutionary link in the origin of pospiviroids
J. Gen. Virol., November 1, 1999; 80(11): 2823 - 2828.
[Abstract] [Full Text]


Home page
J. Gen. Virol.Home page
S. Ambrós, C. Hernández, and R. Flores
Rapid generation of genetic heterogeneity in progenies from individual cDNA clones of peach latent mosaic viroid in its natural host
J. Gen. Virol., August 1, 1999; 80(8): 2239 - 2252.
[Abstract] [Full Text]


Home page
J. Virol.Home page
S. Ambros, C. Hernandez, J. C. Desvignes, and R. Flores
Genomic Structure of Three Phenotypically Different Isolates of Peach Latent Mosaic Viroid: Implications of the Existence of Constraints Limiting the Heterogeneity of Viroid Quasispecies
J. Virol., September 1, 1998; 72(9): 7397 - 7406.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.