Somatic Cell Genetics

, Volume 8, Issue 1, pp 67–81

Mitochondrial DNA analysis of mouse-rat hybrid cells: Effect of chloramphenicol selection on the relative amounts of parental mitochondrial DNAs

  • Jun -Ichi Hayashi
  • Osamu Gotoh
  • Yusaku Tagashira
  • Mariko Tosu
  • Toyozo Sekiguchi
  • Michihiro C. Yoshida
Article

DOI: 10.1007/BF01538651

Cite this article as:
Hayashi, J.I., Gotoh, O., Tagashira, Y. et al. Somat Cell Mol Genet (1982) 8: 67. doi:10.1007/BF01538651

Abstract

Several mouse-rat somatic hybrid cell lines were isolated by fusing chloramphenicol-resistant (CAPR) and CAP-sensitive (CAPS) parent cells, and propagation of the parent mitochondrial DNA (mtDNA) species in the hybrid cells was studied. The restriction endonucleases EcoRI, HpaII, and HaeIII were used for identification of mtDNA species. Both mouse and rat mtDNAs were propagated in all the hybrid cells examined and maintained during long-term cultivation and repeated cell division. Moreover, in CAPR mouse-rat hybrid cells, selection and successive cultivation in the presence of CAP did not increase the relative amount of mtDNA species of CAPR parent cell origin, and when CAP was removed from the culture medium, mtDNA species of CAPR parent cell origin did not decrease appreciably. The amount of mouse mtDNAs was consistently 1–4 times that of rat mtDNAs in the mouse-rat hybrid cells regardless of the species of parent cells from which the CAP resistance was derived. Thus mouse-rat hybrid cells have a stable mtDNA population in which the amount of mouse mtDNAs is larger than that of rat mtDNAs without any influence of CAP selection.

Copyright information

© Plenum Publishing Corporation 1982

Authors and Affiliations

  • Jun -Ichi Hayashi
    • 1
  • Osamu Gotoh
    • 1
  • Yusaku Tagashira
    • 1
  • Mariko Tosu
    • 2
  • Toyozo Sekiguchi
    • 2
  • Michihiro C. Yoshida
    • 3
  1. 1.Department of BiochemistrySaitama Cancer Center Research InstituteSaitamaJapan
  2. 2.Division of RadiobiologyNational Cancer Center Research InstituteTokyoJapan
  3. 3.Chromosome Research Unit, Facility of ScienceHokkaido UniversitySapporoJapan