Single base substitution in an intron of oxidase gene compensates splicing defects of the cytochrome b gene View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1982-08

AUTHORS

Geneviève Dujardin, Claude Jacq, Piotr P. Slonimski

ABSTRACT

An extragenic suppressor mutation, mim2-1, which compensates yeast mitochondrial mutants deficient in splicing of the cytochrome b gene, has been mapped and sequenced. The mutation is due to a single G leads to A transition in the long open reading frame of the fourth intron of the oxidase subunit one gene. It causes the replacement of a glutamic codon by a lysine codon and the expression of a novel mRNA maturase active in splicing. Evolution and regulatory connections between homologous introns of nonhomologous genes are discussed. More... »

PAGES

628

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/298628a0

DOI

http://dx.doi.org/10.1038/298628a0

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1036478387

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/6285204


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