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3'-End formation of transcripts from the yeast rRNA operon
The EMBO Journal
|October 1, 1986
Summary
A specific DNA fragment is essential for correct 3'-end formation in ribosomal RNA (rRNA) transcripts in yeast. This finding suggests a shared processing factor for 37S and 5S pre-rRNA maturation.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- Ribosomal RNA (rRNA) synthesis and processing are fundamental to cellular function.
- Understanding the precise mechanisms of rRNA maturation is crucial for comprehending gene expression regulation.
Purpose of the Study:
- To identify the DNA sequences responsible for the 3'-end formation of Saccharomyces cerevisiae 26S rRNA.
- To investigate the relationship between the processing of different pre-rRNA molecules.
Main Methods:
- Deletion analysis of artificial rRNA minigenes in Saccharomyces cerevisiae.
- Analysis of rRNA transcripts in wild-type and rna 82.1 mutant yeast strains.
- Comparative sequence analysis of rRNA genes from different yeast species.
Main Results:
- A 110 bp fragment (-36 to +74) is necessary and sufficient for correct 3'-end processing of 26S rRNA and 37S pre-rRNA.
- The rna 82.1 mutation affects rRNA processing, indicating a common factor for 37S and 5S pre-rRNA maturation.
- Conserved sequence blocks in intergenic regions suggest roles in processing factor interaction.
Conclusions:
- A common endonuclease likely processes both 37S and 5S pre-rRNAs.
- Specific DNA sequences within the rRNA gene are critical for accurate transcript termination and processing.
- A potential RNA polymerase I terminator site was identified downstream of the rRNA coding region.