NONDEFECTIVE ROTAVIRUS MUTANTS WITH AN NSP1 GENE WHICH HAS A DELETIONOF 500 NUCLEOTIDES, INCLUDING A CYSTEINE-RICH ZINC-FINGER MOTIF-ENCODING REGION (NUCLEOTIDE-156 TO NUCLEOTIDE-248), OR WHICH HAS A NONSENSECODON AT NUCLEOTIDE-153 TO NUCLEOTIDE-155

Citation
K. Taniguchi et al., NONDEFECTIVE ROTAVIRUS MUTANTS WITH AN NSP1 GENE WHICH HAS A DELETIONOF 500 NUCLEOTIDES, INCLUDING A CYSTEINE-RICH ZINC-FINGER MOTIF-ENCODING REGION (NUCLEOTIDE-156 TO NUCLEOTIDE-248), OR WHICH HAS A NONSENSECODON AT NUCLEOTIDE-153 TO NUCLEOTIDE-155, Journal of virology, 70(6), 1996, pp. 4125-4130
Citations number
33
Categorie Soggetti
Virology
Journal title
ISSN journal
0022538X
Volume
70
Issue
6
Year of publication
1996
Pages
4125 - 4130
Database
ISI
SICI code
0022-538X(1996)70:6<4125:NRMWAN>2.0.ZU;2-K
Abstract
We isolated two nondefective bovine rotavirus mutants (A5-10 and A5-16 clones) which have nonsense mutations in the early portion of the ope n reading frame of the NSP1 gene. In the NSP1 gene (1,587 bases long) of A5-10, a nonsense codon is present at nucleotides 153 to 155 just u pstream of the coding region (nucleotides 156 to 230) of a cysteine-ri ch Zn finger motif. A5-16 gene 5 (1,087 bases long) was found to have a large deletion of 500 bases corresponding to nucleotides 142 to 641 of a parent A5-10 NSP1 gene and to have a nonsense codon at nucleotide s 183 to 185, which resulted from the deletion. Expression of gene 5-s pecific NSP1 could not be detected in MA-104 cells infected with the A 5-10 or A5-16 clone or in an in vitro translation system using the pla smids with gene 5 cDNA from A5-10 or A5-16. Nevertheless, both A5-10 a nd A5-16 replicated well in cultured cells, although the plaque size o f A5-16 was extremely small.