Gene mapping by chromosome spot hybridization

Cytometry. 1985 May;6(3):179-85. doi: 10.1002/cyto.990060302.

Abstract

A method is described for the localization of cloned single-copy genes to flow-sorted chromosomes. Chromosomes were sorted directly onto nitrocellulose filters and the chromosomal DNA was subsequently hybridized with gene-specific radioactively labeled DNA probes. Mild aspiration of the filters during sorting was applied to collect the deflected chromosomes in a small spot. Sorting of 10,000-30,000 chromosomes was sufficient to detect gene-specific hybridization with single-copy DNA probes. Using this technique, we have sublocalized the human c-myb oncogene to 6q21-q23 by sorting translocated chromosomes with breakpoints in the q21 and q23 region of chromosome 6. Chromosome spot hybridization appears to be a rapid and simple method to assign cloned genes to chromosomes. Hybridization of an unlocalized gene probe to spots of chromosomes pre-enriched by velocity sedimentation can quickly narrow the choice of chromosomes which need to be sorted. Conversely, individual chromosomes in a flow karyotype can be identified by hybridizing sorted chromosomal DNA with chromosome-specific DNA probes.

MeSH terms

  • Cell Fractionation
  • Cells, Cultured
  • Chromosome Mapping*
  • Cloning, Molecular
  • DNA / genetics
  • Fibroblasts
  • Flow Cytometry
  • Genes*
  • Humans
  • Nucleic Acid Hybridization*
  • Oncogenes

Substances

  • DNA