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
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
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.