Mol Cell Biol, March 1998, p. 1181-1189, Vol. 18, No. 3
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Institute of Cell and Molecular Biology, University of Edinburgh, Edinburgh EH9 3JR, United Kingdom1; EMBL, Heidelberg, Germany2; and LBME-CNRS, 31062 Toulouse Cedex, France3
Received 20 August 1997/Returned for modification 14 October 1997/Accepted 5 December 1997
The genes encoding the small nucleolar RNA (snoRNA) species snR190
and U14 are located close together in the genome of Saccharomyces cerevisiae. Here we report that these two snoRNAs are synthesized by processing of a larger common transcript. In strains mutant for two
5'
3' exonucleases, Xrn1p and Rat1p, families of 5'-extended forms of
snR190 and U14 accumulate; these have 5' extensions of up to 42 and 55 nucleotides, respectively. We conclude that the 5' ends of both snR190
and U14 are generated by exonuclease digestion from upstream processing
sites. In contrast to snR190 and U14, the snoRNAs U18 and U24 are
excised from the introns of pre-mRNAs which encode proteins in their
exonic sequences. Analysis of RNA extracted from a dbr1-
strain, which lacks intron lariat-debranching activity, shows that U24
can be synthesized only from the debranched lariat. In contrast, a
substantial level of U18 can be synthesized in the absence of
debranching activity. The 5' ends of these snoRNAs are also generated
by Xrn1p and Rat1p. The same exonucleases are responsible for the
degradation of several excised fragments of the pre-rRNA spacer
regions, in addition to generating the 5' end of the 5.8S rRNA.
Processing of the pre-rRNA and both intronic and polycistronic snoRNAs
therefore involves common components.
This article has been cited by other articles:
| J. Bacteriol. | J. Virol. | Eukaryot. Cell |
|---|
| Microbiol. Mol. Biol. Rev. | Clin. Vaccine Immunol. | All ASM Journals |
|---|