Universal code equivalent of a yeast mitochondrial intron reading frame is expressed into E. coli as a specific double strand endonuclease.

Abstract

The intron of the mitochondrial 21S rRNA gene of Saccharomyces cerevisiae (r1 intron) possesses a 235 codon long internal open reading frame (r1 ORF) whose translation product determines the duplicative transposition of that intron during crosses between intron-plus strains (omega+) and intron-minus ones (omega-). Using site-directed mutagenesis, we have constructed a universal code equivalent of the r1 ORF that, under appropriate promoter control, allows the overexpression in E. coli of a protein identical to the mitochondrial intron encoded "transposase". This protein exhibits a double strand endonuclease activity specific for the omega- site. This finding demonstrates, for the first time, the enzymatic activity of an intron encoded protein whose function is to promote the spreading of that intron by generating double strand breaks at a specific sequence within a gene.

• Authors: L Colleaux, L d'Auriol, M Betermier, G Cottarel, A Jacquier, F Galibert, B Dujon
• Journal: Cell (Cell) Vol. 44 Issue 4 Pg. 521-33 (Feb 28 1986) ISSN: 0092-8674 [Print] United States
• PMID: 3004738 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• DNA Transposable Elements
• DNA, Mitochondrial
• RNA, Ribosomal
• Nucleotidyltransferases
• Transposases

Topics

• Amino Acid Sequence
• Base Sequence
• Cloning, Molecular
• DNA Transposable Elements
• DNA, Mitochondrial (genetics)
• Escherichia coli (genetics)
• Gene Expression Regulation
• Genetic Code
• Genetic Engineering
• Mutation
• Nucleotidyltransferases (genetics)
• Protein Biosynthesis
• RNA, Ribosomal (genetics)
• Substrate Specificity
• Transposases