Yeast is unable to excise foreign intervening sequences from hybrid gene transcripts.
- 1 March 1983
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 80 (6) , 1496-1500
- https://doi.org/10.1073/pnas.80.6.1496
Abstract
To investigate whether transcripts from foreign split genes are correctly processed in yeast cells we have constructed two hybrid genes by inserting into the split yeast actin gene an intron-containing fragment from either the Acanthamoeba actin I gene or the duck alpha D-globin gene. The hybrid genes were inserted into the autonomously replicating yeast plasmid YRp7, which was then used to transform yeast cells. It was found that the yeast but not the foreign intervening sequences were excised from the chimeric transcripts. This indicates that the recognition of intervening sequences or the splicing mechanism of RNA polymerase II transcripts is not universal.This publication has 36 references indexed in Scilit:
- Actin genes and actin messenger RNA in Acanthamoeba castellaniiJournal of Molecular Biology, 1982
- The isolation and partial characterization of linked αA- and αD-globin genes from a duck DNA recombinant libraryGene, 1982
- Organization and Expression of Eucaryotic Split Genes Coding for ProteinsAnnual Review of Biochemistry, 1981
- The effect of temperature-sensitive RNA mutants on the transcription products from cloned ribosomal protein genes of yeastCell, 1981
- A gene chimaera of SV40 and mouse β-globin is transcribed and properly splicedNature, 1981
- Abnormal expression of chromosomal rabbit β-globin gene in Saccharomyces cerevisiaeNature, 1980
- Rabbit β-globin mRNA production in mouse L cells transformed with cloned rabbit β-globin chromosomal DNANature, 1979
- SV40 recombinants carrying a functional RNA splice junction and polyadenylation site from the chromosomal mouse βmaj globin geneCell, 1979
- The use of thin acrylamide gels for DNA sequencingFEBS Letters, 1978
- Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybridsCell, 1977