Skip to main content
Genetics logoLink to Genetics
. 1974 Dec;78(4):1063–1100. doi: 10.1093/genetics/78.4.1063

Mitochondrial Genetics VII. Allelism and Mapping Studies of Ribosomal Mutants Resistant to Chloramphenicol, Erythromycin and Spiramycin in S. CEREVISIAE

Pierre Netter 1, Eric Petrochilo 1, Piotr P Slonimski 1, Monique Bolotin-Fukuhara 1, Dario Coen 1, Jean Deutsch 1, Bernard Dujon 1
PMCID: PMC1213239  PMID: 4281750

Abstract

We have isolated 15 spontaneous mutants resistant to one or several antibiotics like chloramphenicol, erythromycin and spiramycin. We have shown by several criteria that all of them result from mutations localized in the mitochondrial DNA. The mutations have been mapped by allelism tests and by two- and three-factor crosses involving various configurations of resistant and sensitive alleles associated in cis or in trans with the mitochondrial locus ω which governs the polarity of genetic recombination. A general mapping procedure based on results of heterosexual (ω+ x ω-) crosses and applicable to mutations localized in the polar segment is described and shown to be more resolving than that based on results of homosexual crosses. Mutations fall into three loci which are all linked and map in the following order: ω–RI–RII–RIII. The first locus is very tightly linked with ω while the second is less linked to the first. Mutations of similar resistance phenotype can belong to different loci and different phenotypes to the same locus. Mutations confer antibiotic resistance on isolated mitochondrial ribosomes and delineate a ribosomal segment of the mitochondrial DNA. Homo- and hetero-sexual crosses between mutants of the ribosomal segment and those belonging to the genetically unlinked ATPase locus, OI, have been performed in various allele configurations. The polarity of recombination between RI, RII, RIII and OI decreases as a function of the distance of the R locus from the ω locus rather than as a function of the distance of the R locus from the OI locus.

Full Text

The Full Text of this article is available as a PDF (2.0 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Avner P. R., Coen D., Dujon B., Slonimski P. P. Mitochondrial genetics. IV. Allelism and mapping studies of oligomycin resistant mutants in S. cerevisiae. Mol Gen Genet. 1973 Sep 5;125(1):9–52. doi: 10.1007/BF00292982. [DOI] [PubMed] [Google Scholar]
  2. Deutsch J., Dujon B., Netter P., Petrochilo E., Slonimski P. P., Bolotin-Fukuhara M., Coen D. Mitochondrial genetics. VI. The petite mutation in Saccharomyces cerevisiae: interrelations between the loss of the p+ factor and the loss of the drug resistance mitochondrial genetic markers. Genetics. 1974 Feb;76(2):195–219. doi: 10.1093/genetics/76.2.195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Faye G., Fukuhara H., Grandchamp C., Lazowska J., Michel F., Casey J., Getz G. S., Locker J., Rabinowitz M., Bolotin-Fukuhara M. Mitochondrial nucleic acids in the petite colonie mutants: deletions and repetition of genes. Biochimie. 1973;55(6):779–792. doi: 10.1016/s0300-9084(73)80030-6. [DOI] [PubMed] [Google Scholar]
  4. Fukuhara H., Faye G., Michel F., Lazowska J., Deutsch J., Bolotin-Fukuhara M., slonimski P. P. Physical and genetic organization of petite and grande yeast mitochondrial DNA.I. Studies by RNA-DNA hybridization. Mol Gen Genet. 1974 May 31;130(3):215–238. doi: 10.1007/BF00268801. [DOI] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES