Detection of monoclonal hematopoiesis using restriction fragment length polymorphism (RFLP) of phosphoglycerokinase (PGK) gene in a patient with hypoplastic myelodysplastic syndrome (MDS)

Intern Med. 1993 Mar;32(3):255-6. doi: 10.2169/internalmedicine.32.255.

Abstract

A clonal analysis of hematopoiesis in a hypoplastic MDS patient was performed. Monoclonal utilization of PGK gene on her two X chromosomes was detected by Southern blot analysis of the bone marrow cells using a PGK probe after methylation-sensitive restriction enzyme treatment. This is compatible with monoclonal construction of her hematopoiesis, confirming MDS nature with a progression of her morphological dysplasia in bone marrow cells. RFLP of PGK gene on X chromosome is thus useful to detect a monoclonality in hematopoietic diseases.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Bone Marrow / pathology
  • Female
  • Hematopoiesis / genetics*
  • Humans
  • Myelodysplastic Syndromes / physiopathology*
  • Phosphoglycerate Kinase / genetics*
  • Polymorphism, Restriction Fragment Length

Substances

  • Phosphoglycerate Kinase