A previously uncharacterized gene, PML, is fused to the retinoic acid receptor alpha gene in acute promyelocytic leukaemia

Leukemia. 1992:6 Suppl 3:117S-119S.

Abstract

It has become apparent that a number of genes disrupted by chromosomal rearrangements during leukaemogenesis encode protein factors involved in transcriptional regulation (20-25) and PML may be another such gene. The replacement of the NH2-terminal transactivation domain in RAR alpha by the PML putative DNA binding and transactivation domains in the PML/RARA fusion produces a novel chimeric protein which may act to block normal myeloid differentiation through disregulation of the genes normally regulated by either or both of the normal proteins.

Publication types

  • Review

MeSH terms

  • Carrier Proteins / genetics*
  • Chromosomes, Human, Pair 15*
  • Chromosomes, Human, Pair 17*
  • Gene Rearrangement
  • Humans
  • Leukemia, Promyelocytic, Acute / genetics*
  • Neoplasm Proteins / genetics*
  • Receptors, Retinoic Acid
  • Transcription Factors / genetics
  • Translocation, Genetic / genetics*
  • Zinc Fingers / genetics

Substances

  • Carrier Proteins
  • Neoplasm Proteins
  • Receptors, Retinoic Acid
  • Transcription Factors