Genes for thrombopoietin and c-mpl are not responsible for familial thrombocythaemia: a case study

Br J Haematol. 1998 Feb;100(2):383-6. doi: 10.1046/j.1365-2141.1998.00571.x.

Abstract

The underlying molecular basis for familial thrombocythaemia (FT). an extremely rare form of primary thrombocythaemia which occurs in an autosomal dominant manner, is currently unknown. We have investigated a family with FT and clarified whether we could detect alteration(s) in the genes coding for c-mpl and its ligand, thrombopoietin (TPO). There was no difference in platelet c-mpl mRNA expression levels between the affected and non-affected individuals in the family. Nucleotide sequence analysis of the c-mpl cDNA for the proband revealed no abnormality. We identified an intragenic tetranucleotide short tandem repeat system in the TPO gene and found non-linkage between the TPO locus and the FT phenotype. We conclude that genes for c-mpl and TPO are not responsible for thrombocythaemia in our FT family.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Blood Platelets / metabolism
  • DNA / metabolism
  • Humans
  • Male
  • Neoplasm Proteins*
  • Pedigree
  • Proto-Oncogene Proteins / genetics*
  • Receptors, Cytokine*
  • Receptors, Thrombopoietin
  • Thrombocytosis / genetics*
  • Thrombocytosis / metabolism
  • Thrombopoietin / genetics*
  • Thrombopoietin / metabolism

Substances

  • Neoplasm Proteins
  • Proto-Oncogene Proteins
  • Receptors, Cytokine
  • Receptors, Thrombopoietin
  • MPL protein, human
  • DNA
  • Thrombopoietin