Analysis of chromosome 6 deletions in lymphoid malignancies provides evidence for a region of minimal deletion within a 2-megabase segment of 6q21

Chromosome Res. 1997 Apr;5(2):118-24. doi: 10.1023/a:1018418224660.

Abstract

Fluorescence in situ hybridization has been used to define deletion breakpoints within chromosome bands 6q16-21 in cases of lymphoid malignancy. Previous evidence suggested that the region might contain a tumour-suppressor gene. Six yeast artificial chromosome probes, each selected using a single marker, were localized to 6q16-21 and the following order was confirmed; D6S330-D6S283-D6S301-D6S447-D6S246-FYN+ ++. Of 32 cases of lymphoid malignancy, 30 showed deletion of D6S246 and, in the two cases in which D6S246 was retained, the adjacent marker, D6S447, was deleted. These observations imply that a region of minimal deletion is located within a 2-megabase segment of 6q21, between D6S447 and D6S246, providing a candidate region for the location of a tumour-suppressor gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor
  • Chromosome Deletion*
  • Chromosome Mapping
  • Chromosomes, Artificial, Yeast
  • Chromosomes, Human, Pair 6 / genetics*
  • DNA Probes
  • Genes, Tumor Suppressor / genetics
  • Humans
  • In Situ Hybridization, Fluorescence / methods
  • Karyotyping
  • Lymphoma, Non-Hodgkin / genetics*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Sequence Tagged Sites

Substances

  • Biomarkers, Tumor
  • DNA Probes