Deletion of the 3q26 region including the EVI1 and MDS1 genes in a neonate with congenital thrombocytopenia and subsequent aplastic anaemia

J Med Genet. 2012 Sep;49(9):598-600. doi: 10.1136/jmedgenet-2012-100990.

Abstract

Background: Gene-targeting studies in mice have revealed a key role for EVI1 protein in the maintenance of haematopoiesis, and argue in favour of a gene dosage requirement for EVI1 in the regulation of haematopoietic stem cells. Furthermore, a fusion transcript of MDS1 and EVI1 has been shown to play a critical role in maintaining long-term haematopoietic stem cell function. Inappropriate activation of EVI1, usually due to a translocation, is a well known and unfavourable change in several myeloid malignancies. It is not known whether haploinsufficiency of any of these genes leads to disease in humans.

Methods: SNP array analysis in a patient with in a neonate with congenital thrombocytopenia and subsequent aplastic anaemia

Results and conclusions: We report for the first time a constitutional deletion encompassing the EVI1 and MDS1 genes in a human, and argue that the deletion causes congenital bone marrow failure in this patient.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Anemia, Aplastic / complications
  • Anemia, Aplastic / genetics*
  • Chromosomes, Human, Pair 3 / genetics*
  • DNA-Binding Proteins / genetics*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • MDS1 and EVI1 Complex Locus Protein
  • Male
  • Polymorphism, Single Nucleotide / genetics
  • Pregnancy
  • Proto-Oncogenes / genetics*
  • Sequence Deletion / genetics*
  • Thrombocytopenia / congenital*
  • Thrombocytopenia / genetics*
  • Transcription Factors / genetics*

Substances

  • DNA-Binding Proteins
  • MDS1 and EVI1 Complex Locus Protein
  • MECOM protein, human
  • Transcription Factors