Chromosome aberrations associated with CAD gene amplification in Chinese hamster cultured cells

Mutat Res. 1988 May;199(1):111-21. doi: 10.1016/0027-5107(88)90236-9.

Abstract

Eleven sublines with increasing resistance to N-phosphonacetyl-L-aspartate (PALA) were isolated from the V79,B7 Chinese hamster cell line. Aspartate transcarbamylase activity and CAD gene copy number increased with increasing resistance of sublines. In situ hybridization with a DNA probe for the CAD gene showed that the amplified sequences resided in the terminal region of a marker chromosome with elongated q arms. This region stained homogeneously after G-banding. A high incidence of both numerical and structural chromosome aberrations was found in PALA-resistant cells. In hyperdiploid and polyploid cells, containing 2 copies of the marker chromosome, dicentrics were found at a very high frequency. As indicated by in situ hybridization and G-banding, they originated from a rearrangement involving 2 homologous marker chromosomes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aspartate Carbamoyltransferase / genetics
  • Aspartic Acid / analogs & derivatives
  • Aspartic Acid / pharmacology
  • Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing) / genetics
  • Cell Line
  • Chromosome Aberrations*
  • Chromosome Banding
  • Cricetinae
  • Cricetulus
  • Dihydroorotase / genetics
  • Drug Resistance
  • Gene Amplification*
  • Genes
  • Multienzyme Complexes / genetics*
  • Neoplasm Proteins / genetics*
  • Phosphonoacetic Acid / analogs & derivatives
  • Phosphonoacetic Acid / pharmacology

Substances

  • CAD trifunctional enzyme
  • Multienzyme Complexes
  • Neoplasm Proteins
  • Aspartic Acid
  • sparfosic acid
  • Aspartate Carbamoyltransferase
  • Dihydroorotase
  • Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing)
  • Phosphonoacetic Acid