A Line 1 insertion in the Factor IX gene segregates with mild hemophilia B in dogs

Mamm Genome. 2003 Nov;14(11):788-95. doi: 10.1007/s00335-003-2290-z.

Abstract

We undertook the biochemical and molecular characterization of hemophilia in a large pedigree of German wirehaired pointers. Males affected with hemophilia B had approximately 5% normal Factor IX coagulant activity and a proportional reduction of Factor IX protein concentration, indicative of a mild hemophilia B phenotype. Using Southern blot analyses and PCR amplification of genomic DNA, we discovered a large, 1.5-kb insertion in intron 5 of the Factor IX gene of an affected male. The insert consists of a 5' truncated canine Line-1 followed by an approximately 200-bp 3' poly (A) tract, flanked by a 15-bp direct repeat. The insert can be traced through at least five generations and segregates with the hemophilia B phenotype in this breed. This is the first description of a Factor IX mutation associated with mild hemophilia B in a non-human species and provides evidence for a recent Line-1 insertion event in the canine genome.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Blotting, Southern
  • DNA Primers
  • Dog Diseases / genetics*
  • Dogs
  • Factor IX / genetics*
  • Factor IX / metabolism
  • Female
  • Hemophilia B / genetics
  • Hemophilia B / veterinary*
  • Introns / genetics
  • Long Interspersed Nucleotide Elements / genetics*
  • Male
  • Molecular Sequence Data
  • Mutation / genetics
  • Pedigree
  • Polymerase Chain Reaction
  • Sequence Analysis, DNA

Substances

  • DNA Primers
  • Factor IX