PROCESSING OF U14 SMALL NUCLEOLAR RNA FROM 3 DIFFERENT INTRONS OF THEMOUSE 70-KDA-COGNATE-HEAT-SHOCK-PROTEIN PREMESSENGER RNA

Citation
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
Citations number
30
Categorie Soggetti
Biology
ISSN journal
00142956
Volume
226
Issue
3
Year of publication
1994
Pages
765 - 771
Database
ISI
SICI code
0014-2956(1994)226:3<765:POUSNR>2.0.ZU;2-A
Abstract
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.