Sequence analysis of mitochondrial chloramphenicol resistance mutations in Chinese hamster cells

Mamm Genome. 1993;4(5):271-5. doi: 10.1007/BF00417434.


A series of mitochondrially inherited chloramphenicol-resistant (CAP-R) mutants were isolated in Chinese hamster cells. To determine whether the Chinese hamster CAP-R mutations were homologous to those isolated in mouse and human cell culture systems, we determined the nucleotide sequence of the region of the mitochondrial 16S rRNA gene spanning the peptidyl transferase-encoding region for eight CAP-R mutant lines in addition to the parental wild-type line. Three main conclusions are drawn from these studies. (1) Although the region of the gene encoding the peptidyl transferase domain is highly conserved relative to that of mice and rats, the contiguous sequences show less conservation. This sequence divergence not only includes the accumulation of single base pair replacements, but also the presence of small insertions or deletions. (2) For six of the CAP-R mutants, heteroplasmic single base pair changes were detected. These mapped to the same sites within the peptidyl transferase domain as the mutations found previously in mouse and human CAP-R mutants. (3) Two Chinese hamster CAP-R mutants, both with an unusual drug resistance phenotype, did not carry any mutations within the CAP-R peptidyl transferase domain. However, both carried a heteroplasmic mutation at the position corresponding to nucleotide 2505 of the mouse 16S rRNA gene, a site predicted to map within a stem/loop structure attached to this key domain of the ribosome. This is the first evidence for mitochondrial CAP-R mutations that map outside the peptidyl transferase region.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Chloramphenicol Resistance / genetics*
  • Conserved Sequence
  • Cricetinae
  • Cricetulus
  • DNA / genetics
  • Humans
  • Mice
  • Mitochondria / metabolism
  • Molecular Sequence Data
  • Mutation
  • Peptidyl Transferases / genetics
  • Phenotype
  • RNA, Ribosomal, 16S / genetics
  • Rats
  • Sequence Homology, Nucleic Acid


  • RNA, Ribosomal, 16S
  • DNA
  • Peptidyl Transferases