Nonsense and missense mutations in hemophilia A: estimate of the relative mutation rate at CG dinucleotides

Am J Hum Genet. 1988 May;42(5):718-25.

Abstract

Hemophilia A is an X-linked disease of coagulation caused by deficiency of factor VIII. Using cloned cDNA and synthetic oligonucleotide probes, we have now screened 240 patients and found CG-to-TG transitions in an exon in nine. We have previously reported four of these patients; and here we report the remaining five, all of whom were severely affected. In one patient a TaqI site was lost in exon 23, and in the other four it was lost in exon 24. The novel exon 23 mutation is a CG-to-TG substitution at the codon for amino acid residue 2166, producing a nonsense codon in place of the normal codon for arginine. Similarly, the exon 24 mutations are also generated by CG-to-TG transitions, either on the sense strand producing nonsense mutations or on the antisense strand producing missense mutations (Arg to Gln) at position 2228. The novel missense mutations are the first such mutations observed in association with severe hemophilia A. These results provide further evidence that recurrent mutations are not uncommon in hemophilia A, and they also allow us to estimate that the extent of hypermutability of CG dinucleotides is 10-20 times greater than the average mutation rate for hemophilia A.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Antigens / genetics
  • Base Sequence
  • Cytosine
  • DNA / blood
  • DNA / genetics
  • DNA Restriction Enzymes
  • Dinucleoside Phosphates
  • Factor VIII / genetics*
  • Female
  • Genes*
  • Guanine
  • Hemophilia A / genetics*
  • Humans
  • Leukocytes / metabolism
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Mutation*
  • Oligonucleotides / genetics*
  • Pedigree
  • Polymorphism, Genetic

Substances

  • Antigens
  • Dinucleoside Phosphates
  • Oligonucleotides
  • Guanine
  • Cytosine
  • Factor VIII
  • DNA
  • DNA Restriction Enzymes