CHARACTERIZATION AND DETECTION OF SC4 - A 6TH GENE ENCODED BY SONCHUSYELLOW NET VIRUS

Citation
Kbg. Scholthof et al., CHARACTERIZATION AND DETECTION OF SC4 - A 6TH GENE ENCODED BY SONCHUSYELLOW NET VIRUS, Virology, 204(1), 1994, pp. 279-288
Citations number
50
Categorie Soggetti
Virology
Journal title
ISSN journal
00426822
Volume
204
Issue
1
Year of publication
1994
Pages
279 - 288
Database
ISI
SICI code
0042-6822(1994)204:1<279:CADOS->2.0.ZU;2-3
Abstract
The nucleotide sequence of a sixth gene (sc4) of the plant rhabdovirus sonchus yellow net virus (SYNV) was determined from viral genomic and poly(A)C cDNA clones. The sc4 gene is 1196 nucleotides (nt) and has a n open reading frame of 972 nt that is capable of encoding a protein o f 324 amino acids. Primer extension analyses of poly(A)(+) RNA isolate d from infected plants indicate that the 5' end of the sc4 mRNA corres ponds to nucleotide 2840, relative to the 3' end of the minus-sense ge nomic RNA and extends to nucleotide 4035. A 43-nt untranslated leader sequence precedes the predicted first AUG codon and a 181-nt untransla ted sequence follows the translational stop codon. This gene is simila r to the other SYNV genes in that it is flanked on each side by a cons erved gene junction sequence. Polyclonal antibodies raised to an sc4 f usion protein react with a 37-kDa protein in virus-infected plants tha t is close to the predicted size of the sc4 protein. Western blot anal yses of cellular fractionations from infected plants show that sc4 is membrane associated and sucrose density gradient analyses demonstrate that sc4 sediments in the same fractions as SYNV virions. Analysis of the sc4 open reading frame reveals that 16% of the amino acids are ser ine or threonine residues and that the protein has four potential cons ensus casein kinase II phosphorylation sites. The deduced amino acid s equence of sc4 also contains a motif related to alpha amylases and asp artic proteases. This completes the sequence determination of the 13,7 20-nt SYNV genome. (C) 1994 Academic Press, Inc.