Aberrant histone modifications induced by mutant ASXL1 in myeloid neoplasms

Int J Hematol. 2019 Aug;110(2):179-186. doi: 10.1007/s12185-018-2563-7. Epub 2018 Dec 5.

Abstract

An epigenetic modulator Additional sex combs-like 1 (ASXL1) is recurrently mutated in myeloid neoplasms such as myelodysplastic syndromes (MDS), acute myeloid leukemia (AML) and myeloproliferative neoplasms (MPNs). ASXL1 mutations are also frequently detected in clonal hematopoiesis with indeterminate potential (CHIP), which is the clonal expansion of premalignant hematopoietic cells without any evidence of hematological malignancies. Thus, understanding the roles of ASXL1 in hematopoiesis and myeloid neoplasms is a clinically crucial issue. ASXL1 mutations in hematological neoplasms are typically frameshift or nonsense mutations and occur near the 5' end of the last exon, thereby the transcripts would escape from nonsense-mediated decay, Indeed, we identified the C-terminally truncated mutant protein of ASXL1 in several cell lines derived from patients with myeloid leukemia. In mouse models, expression of the mutant ASXL1 results in impaired hematopoiesis and promotes development of myeloid neoplasms. In addition, recent findings from biochemical analysis have demonstrated that the mutant ASXL1 protein gains new functions including enhancing catalytic activity of BRCA1-associated protein 1 (BAP1), resulting in reduction of H2AK119ub and aberrant gene expression essential for myeloid transformation. In this review, we will focus on the pivotal roles of the mutant ASXL1 on histone modifications and myeloid transformation.

Keywords: ASXL1; BAP1; H2AK119ub; Histone modifications; Myeloid neoplasms.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Transformation, Neoplastic / genetics
  • Codon, Nonsense
  • Frameshift Mutation
  • Gain of Function Mutation
  • Gene Expression Regulation, Leukemic
  • Hematopoiesis / genetics
  • Histone Code*
  • Homeodomain Proteins / metabolism
  • Humans
  • Leukemia, Experimental / genetics
  • Leukemia, Experimental / physiopathology
  • Leukemia, Myeloid, Acute / genetics*
  • Mice
  • Molecular Targeted Therapy
  • Multiprotein Complexes / physiology
  • Myelodysplastic Syndromes / genetics*
  • Myeloproliferative Disorders / genetics*
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / physiology
  • Protein Processing, Post-Translational
  • Repressor Proteins / deficiency
  • Repressor Proteins / genetics*
  • Repressor Proteins / physiology
  • Structure-Activity Relationship
  • Tumor Suppressor Proteins / physiology
  • Ubiquitin Thiolesterase / physiology
  • Ubiquitination

Substances

  • ASXL1 protein, human
  • BAP1 protein, human
  • Codon, Nonsense
  • Homeodomain Proteins
  • Multiprotein Complexes
  • Neoplasm Proteins
  • Repressor Proteins
  • Tumor Suppressor Proteins
  • HoxA protein
  • Ubiquitin Thiolesterase