A polymorphic marker for the human cathepsin B gene

Mol Cell Probes. 2001 Aug;15(4):235-7. doi: 10.1006/mcpr.2001.0362.

Abstract

Human cathepsin B (CTSB) is a proteolytic enzyme implicated in tumor invasion and metastasis. We describe a PCR-based polymorphic marker for this gene comprising two amplimers differing in length by 19 consecutive nucleotides in intron 7, near the exon 8 splice acceptor site, identifying two gene alleles (A and B). Allele frequencies were 0.614 for A and 0.386 for the B allele, with an observed heterozygosity of 0.457 in a cohort of 70 non-related Australian blood donors. One additional nucleotide difference was also revealed through sequencing. The human CTSB gene is located on chromosome 8 and the alleles described here can potentially be used as markers in linkage and association studies of cancers and other diseases.

MeSH terms

  • Alleles
  • Australia
  • Base Sequence
  • Cathepsin B / genetics*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 8 / genetics
  • Exons
  • Gene Frequency / genetics
  • Genetic Markers / genetics
  • Genotype
  • Humans
  • Introns
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Polymorphism, Genetic / genetics*

Substances

  • Genetic Markers
  • Cathepsin B