Recurrence of OTT-MAL fusion in t(1;22) of infant AML-M7

Genes Chromosomes Cancer. 2002 Jan;33(1):22-8. doi: 10.1002/gcc.1208.

Abstract

Translocation t(1;22)(p13;q13) is associated with a peculiar subtype of acute megakaryocytic leukemia (M7) occurring in infants. We have recently characterized a fusion gene, OTT-MAL, resulting from this translocation. We now report three additional cases and show that this gene fusion is present in all five t(1;22) cases studied to date. Nucleotide sequence analysis of two translocation breakpoints suggests a nonhomologous end joining mechanism in the genesis of this translocation and reveals a noncanonical topoisomerase II-like consensus sequence within the OTT gene. FISH and PCR techniques described in this work are useful for identifying t(1;22) associated with M7.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Chromosome Painting
  • Chromosomes, Human, Pair 1 / genetics*
  • Chromosomes, Human, Pair 22 / genetics*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Infant, Newborn
  • Leukemia, Megakaryoblastic, Acute / diagnosis
  • Leukemia, Megakaryoblastic, Acute / genetics*
  • Male
  • Molecular Sequence Data
  • Oncogene Proteins, Fusion / genetics
  • Proteins / genetics*
  • RNA-Binding Proteins*
  • Translocation, Genetic / genetics*

Substances

  • Oncogene Proteins, Fusion
  • Proteins
  • RBM15 protein, human
  • RNA-Binding Proteins