Size and position of intervening sequences are critical for the splicing efficiency of pre-mRNA in the yeastSaccharomyces cerevisiae
Open Access
- 11 June 1985
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 13 (11) , 3791-3804
- https://doi.org/10.1093/nar/13.11.3791
Abstract
The size of the 309 bp actin gene Intron of the yeast Saccharomyces cerevisiae was enlarged by inserting DNA fragments of different lengths and sequence. Enlarging the intron above 551 bp, the largest known yeast intron, led to a decrease in splicing efficiency. The effect on transcript splicing was dependent on the length of the inserted fragments rather then their sequence. It was also observed that insertion of the actin gene intron into different regions of the normally unsplit yeast YP2 gene, significantly influenced the efficiency of splicing of the resulting transcripts. The splicing efficiency decreased with the increase of the distance between the mRNA cap site and the intervening sequenceKeywords
This publication has 40 references indexed in Scilit:
- In vivo splicing products of the rabbit β-globin pre-mRNACell, 1984
- Lariat structures are in vivo intermediates in yeast pre-mRNA splicingCell, 1984
- Characterization of the human factor VIII geneNature, 1984
- Identification of the pleiotropic cell division cycle gene NDA2 as one of two different α-tubulin genes in schizosaccharomyces pombeCell, 1984
- Point mutations identify the conserved, intron-contained TACTAAC box as an essential splicing signal sequence in yeastCell, 1984
- A yeast gene encoding a protein homologous to the human c-has/bas proto-oncogene productNature, 1983
- Evidence for an intron-contained sequence required for the splicing of yeast RNA polymerase II transcriptsCell, 1983
- Isolation of the β-tubulin gene from yeast and demonstration of its essential function in vivoCell, 1983
- Organization and Expression of Eucaryotic Split Genes Coding for ProteinsAnnual Review of Biochemistry, 1981
- Comparison of Total Sequence of a Cloned Rabbit β-Globin Gene and Its Flanking Regions with a Homologous Mouse SequenceScience, 1979