Molecular and General Genetics MGG

, Volume 163, Issue 3, pp 257–275

Restriction enzyme analysis of mitochondrial DNAs of petite mutants of yeast: Classification of petites, and deletion mapping of mitochondrial genes

Authors

  • Alfred Lewin
    • Department of MedicineThe University of Chicago Pritzker School of Medicine
    • Department of BiochemistryThe University of Chicago Pritzker School of Medicine
    • Department of BiologyThe University of Chicago Pritzker School of Medicine
    • Franklin McLean Memorial Research Institute
  • Richard Morimoto
    • Department of MedicineThe University of Chicago Pritzker School of Medicine
    • Department of BiochemistryThe University of Chicago Pritzker School of Medicine
    • Department of BiologyThe University of Chicago Pritzker School of Medicine
    • Franklin McLean Memorial Research Institute
  • Murray Rabinowitz
    • Department of MedicineThe University of Chicago Pritzker School of Medicine
    • Department of BiochemistryThe University of Chicago Pritzker School of Medicine
    • Department of BiologyThe University of Chicago Pritzker School of Medicine
    • Franklin McLean Memorial Research Institute
  • Hiroshi Fukuhara
    • Section de BiologieFoundation Curie Institut du Radium
Article

DOI: 10.1007/BF00271955

Cite this article as:
Lewin, A., Morimoto, R., Rabinowitz, M. et al. Molec. Gen. Genet. (1978) 163: 257. doi:10.1007/BF00271955

Summary

We have analyzed the restriction digest patterns of the mitochondrial DNA from 41 cytoplasmic petite strains of Saccharomyces cerevisiae, that have been extensively characterized with respect to genetic markers. Each mitochondrial DNA was digested with seven restriction endonucleases (EcoRI, HpaI, HindIII, BamHI, HhaI, SalI, and PstI) which together make 41 cuts in grande mitochondrial DNA and for which we have derived fragment maps. The petite mitochondrial DNAs were also analyzed with HpaII, HaeIII, and AluI, each of which makes more than 80 cleavages in grande mitochondrial DNA. On the basis of the restriction patterns observed (i.e., only one fragment migrating differently from grande for a single deletion, and more than one for multiple deletions) and by comparing petite and grande mitochondrial DNA restriction maps, the petite clones could be classified into two main groups: (1) petites representing a single deletion of grande mitochondrial DNA and (2) petites containing multiple deletions of the grande mitochondrial DNA resulting in rearranged sequences. Single deletion petites may retain a large portion of the grande mitochondrial genome or may be of low kinetic cimplexity. Many petites which are scored as single continuous deletions by genetic criteria were later demonstrated to be internally deleted by restriction endonuclease analysis. Heterogeneous sequences, manifested by the presence of sub-stoichiometric amounts of some restriction fragments, may accompany the single or multiple deletions. Single deletions with heterogeneous sequences remain useful for mapping if the low concentration sequences represent a subset of the stoichiometric bands. Using a group of petites which retain single continuous regions of the grande mitochondrial DNA, we have physically mapped antibiotic resistance and mit- markers to regions of the grande restriction map as follows: C (99.3-1.4 map units)-OXI-1 (2.5-15.7)-OXI-2 (18.5-25)-P (28.1-34.2)-OXI-3 (32.2-61.2)-OII (60-62)-COB (64.6-80.8)-OI (80.4-85.7)-E (95-98.9).

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Copyright information

© Springer-Verlag 1978