The FANCA gene in Japanese Fanconi anemia: reports of eight novel mutations and analysis of sequence variability

Hum Mutat. 1999;13(3):237-44. doi: 10.1002/(SICI)1098-1004(1999)13:3<237::AID-HUMU8>3.0.CO;2-F.

Abstract

Fanconi anemia (FA), an autosomal recessive disorder characterized by a progressive pancytopenia associated with congenital anomalies and high predisposition to malignancies, is a genetically and clinically heterogeneous disease. At least eight complementation groups (FA-A to FA-H) have been identified with their relative prevalence varying among the ethnical backgrounds. Recently, responsible genes, FANCA and FANCC, have been cloned. This report describes mutations of the FANCA gene, which we studied by direct sequencing of cDNA with confirmation on genomic DNA in 15 unclassified Japanese FA patients. A total of 19 sequence alterations were identified, of which 10 (six missense and four silent alterations) were likely to be nonpathogenic polymorphism. The remaining nine alterations, of which eight were novel mutations, were assumed to be pathogenic and consisted of two missense mutations and seven mutations resulting in truncation of gene product, demonstrating a wide allelic heterogeneity. The pathogenic mutations were found in 12 patients (80%); they were either homozygous or compound heterozygous in 10 patients, apparently heterozygous in two patients and none in three patients. We conclude that the sequence variability is intrinsic to the FANCA gene and that the relative prevalence of the FA-A subtype is unusually high in Japanese FA patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Mutational Analysis
  • DNA Primers
  • Databases, Factual
  • Exons
  • Fanconi Anemia / genetics*
  • Female
  • Gene Deletion
  • Genetic Testing
  • Humans
  • Introns
  • Japan
  • Male
  • Models, Genetic
  • Mutation*
  • Mutation, Missense
  • Point Mutation
  • Polymorphism, Genetic
  • Polymorphism, Restriction Fragment Length
  • RNA Splicing
  • Reverse Transcriptase Polymerase Chain Reaction
  • Trinucleotide Repeat Expansion

Substances

  • DNA Primers