Signals Sufficient for 3′-End Formation of Yeast mRNA
Open Access
- 1 June 1996
- journal article
- research article
- Published by Taylor & Francis in Molecular and Cellular Biology
- Vol. 16 (6) , 2772-2776
- https://doi.org/10.1128/mcb.16.6.2772
Abstract
The following three elements were previously shown to be required for 39-end formation of mRNA in the yeast Saccharomyces cerevisiae: (i) the efficiency element TATATA or related sequences, which function by enhancing the efficiency of downstream positioning elements; (ii) the positioning element AATAAA or related sequences, which position the poly(A) site; and (iii) the actual poly(A) site, which is usually Py(A)n. In this study, we synthesized a 39-pb poly(A) signal that contained the optimum sequences of these three elements. By inserting the synthetic 39-end-forming signal into various positions of a CYC1-lacZ fusion gene, we showed that truncated transcripts of the expected sizes were generated. Furthermore, the poly(A) sites of the truncated transcripts were mapped to the expected poly(A) site within the synthetic signal. Our findings establish that the three elements are not only necessary but also sufficient for mRNA 39-end formation in S. cerevisiae.Keywords
This publication has 26 references indexed in Scilit:
- Redundant 3' end-forming signals for the yeast CYC1 mRNA.Proceedings of the National Academy of Sciences, 1995
- Saturation mutagenesis of a polyadenylation signal reveals a hexanucleotide element essential for mRNA 3' end formation in Saccharomyces cerevisiae.Proceedings of the National Academy of Sciences, 1994
- THE BIOCHEMISTRY OF 3′-END CLEAVAGE AND POLYADENYLATION OF MESSENGER RNA PRECURSORSAnnual Review of Biochemistry, 1992
- RNA Processing Generates the Mature 3′ End of Yeast CYC1 Messenger RNA in VitroScience, 1988
- Transcription by RNA polymerase II induces changes of DNA topology in yeast.Genes & Development, 1988
- Transcription terminates in yeast distal to a control sequenceCell, 1983
- Heme regulates transcription of the CYC1 gene of S. cerevisiae via an upstream activation siteCell, 1983
- DNA sequence required for efficient transcription termination in yeastCell, 1982
- Complete Nucleotide Sequence of the Escherichia coli Plasmid pBR322Published by Cold Spring Harbor Laboratory ,1979
- DNA sequencing with chain-terminating inhibitorsProceedings of the National Academy of Sciences, 1977