Genetic analysis of a vital mammalian housekeeping locus using CHO cells that express a transfected mutant allele

Somat Cell Mol Genet. 1990 Nov;16(6):517-28. doi: 10.1007/BF01233092.

Abstract

We describe a novel approach for the isolation of null mutations in a vital Chinese hamster ovary (CHO) cell housekeeping gene. Our experimental strategy required introduction of an expressible DNA clone encoding a recessive emetine-resistance allele of ribosomal protein S14 into wild-type CHO cells. Transgene heterozygote (TGH) cell lines, which harbor multiple emetine-resistance S14 transgenes, survive mutations that inactivate the CHO RPS14 locus by virtue of the transgenes' biological function. Null mutations in RPS14 yield TGH clones that display the transgene's drug-resistance phenotype. A large collection of emetine-resistant clones was isolated from one TGH cell line and shown to consist of three types of S14 mutations: (1) nonsense null mutations in the RPS14 protein coding sequence; (2) missense null mutations that affect S14 amino acid residues that have been conserved stringently during eukaryotic evolution; and (3) a recurrent missense mutation that results in a new, functional RPS14 emetine-resistance allele.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Line
  • Cloning, Molecular
  • Cricetinae
  • Cricetulus
  • Electrophoresis, Gel, Two-Dimensional
  • Molecular Sequence Data
  • Mutation
  • Protein Biosynthesis
  • RNA, Messenger / genetics
  • Restriction Mapping
  • Ribosomal Proteins / genetics*
  • Transcription, Genetic
  • Transfection

Substances

  • RNA, Messenger
  • Ribosomal Proteins
  • ribosomal protein S14