H. Barbhaiya et al., PROCESSING OF U14 SMALL NUCLEOLAR RNA FROM 3 DIFFERENT INTRONS OF THEMOUSE 70-KDA-COGNATE-HEAT-SHOCK-PROTEIN PREMESSENGER RNA, European journal of biochemistry, 226(3), 1994, pp. 765-771
U14 is a small nucleolar RNA required for the processing of eukaryotic
rRNA precusors. The U14 genes of mouse as well as rat, hamster, human
, Xenopus and trout are encoded within introns of the constitutively e
xpressed 70-kDa-cognate-heat-shock protein gene (hsc70). We demonstrat
e here that U14.6 and U14.8 snRNAs, in addition to the previously char
acterized U14.5, are processed from their respective introns when hsc7
0 pre-mRNA transcripts containing these intronic snRNAs are injected i
nto Xenopus oocyte nuclei. Identical intermediates are observed in the
processing of all three mouse U14 snRNAs indicating similar processin
g pathways. The production of U14 snRNA processing intermediates posse
ssing either mature 5' or 3' termini demonstrated that processing can
occur at either end independent of maturation at the other terminus. P
rocessing of U14.6 from hsc70 intron 6 is not dependent upon the base
pairing of intron sequences flanking the 5' and 3' termini of the enco
ded U14 snRNA molecule. Therefore, excision of an intronic snRNA does
not require extending the 5',3' terminal helix of U14 snRNA secondary
structure into flanking intron regions as originally suggested. Microi
njection of the plasmid vector containing the mouse hsc70/U14.5 snRNA
coding region revealed that undetermined plasmid sequences can serve a
s non-specific promoters to generate spurious RNA transcripts. The pro
cessing of these transcripts and examination of the plasmid-initiated
transcriptional-start sites indicated that a U14-specific promoter is
not present in or around the intron-encoded U14.5 gene. These results
strongly suggest that biosynthesis of mouse U14 snRNA results from an
intron-processing pathway.