More than 80 group I introns were detected and characterized in Chlore
lla viruses isolated from various locations in Japan; the overall aver
age frequency of viruses containing the group I intron was 8.0%. Altho
ugh most of these introns were inserted in the gene for either transcr
iptional elongation factor TFIIS (similar to 60%) or URF14.2 (unidenti
fied open reading frame coding for a 14.2-kDa polypeptide) (similar to
40%), in a few cases, the gene for the major capsid protein Vp52 cont
ained an intron. These introns were biologically active (self-splicing
) both in vivo and in vitro. Viruses that contained introns almost usu
ally contained only one, but more than two introns coexisted in severa
l virus isolates. Nucleotide sequence analysis showed that the intron
sequences have diverged under strong constraint of the exon genes: int
rons in the same gene showed more than 99% sequence identity, whereas
introns in different genes were only 72-78% identical. Phylogenetic an
alysis suggested relatedness of these introns to those found in the rR
NA genes of a variety of organisms including green algae, red algae, y
easts, fungi, and protozoa. (C) 1998 Academic Press.