Characterization of a large chromosomal deletion in the PROS1 gene of a patient with protein S deficiency type I using long PCR

Br J Haematol. 1996 Mar;92(4):986-91. doi: 10.1046/j.1365-2141.1996.403943.x.

Abstract

A long-PCR-based technique was developed to investigate a possible deletion in the protein S gene, PROS1, in a family with type I protein S (PS) deficiency (pedigree PS62). Long-PCR across introns produced an unexpected 2kb PCR product between exon VII and XII not seen in control individuals, in addition to the expected 2.5 kb exon VII-VIII product. This result suggested that a deletion had occurred between exons VII and XII in the PS-deficient family members. All were heterozygous for the deletion, Sequencing of the cloned 2 kb fragment gave the precise location of the breakpoints within introns 7 and 11. Significant similarity existed in both introns to repetitive sequences, e.g. Alu and Mer12, but no significant similarity was evident between the two introns themselves. The technique of long-PCR is simple and more informative than Southern blotting in detecting and characterizing large intragenic deletions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Chromosome Deletion*
  • Chromosome Mapping / methods
  • Exons / genetics
  • Humans
  • Introns / genetics
  • Molecular Sequence Data
  • Mutation
  • Polymerase Chain Reaction
  • Protein S / genetics*
  • Protein S Deficiency / genetics*
  • Sequence Analysis, DNA

Substances

  • Protein S

Associated data

  • GENBANK/S81766
  • GENBANK/S81775
  • GENBANK/S81777