First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiency

Blood Coagul Fibrinolysis. 1994 Aug;5(4):593-600.

Abstract

The authors used a strategy combining the amplification-refractory mutations system (ARMS) and denaturing gradient gel electrophoresis (DGGE) to screen the active protein S (PS) gene in a family with PS deficiency, and found a frameshift mutation in exon V. The protein, if expressed, would have an aberrant amino acid sequence from positions 82 to 90 and a premature stop codon in position 91. The mutation co-segregated with the deficient phenotype and was not found in 120 normal chromosomes. It is proposed that the deletion of a T in the codon corresponding to Pro 82 described here is responsible for the deficient phenotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Base Sequence
  • Electrophoresis, Polyacrylamide Gel
  • Exons
  • Female
  • Frameshift Mutation*
  • Humans
  • Male
  • Molecular Sequence Data
  • Pedigree
  • Protein Denaturation
  • Protein S / genetics*
  • Protein S Deficiency / genetics*
  • Pulmonary Embolism
  • Sequence Deletion

Substances

  • Protein S

Associated data

  • GENBANK/S74438