Activation of AML1-mediated transcription by MOZ and inhibition by the MOZ-CBP fusion protein

Issay Kitabayashi, Yukiko Aikawa, Lan Anh Nguyen, Akihiko Yokoyama, Misao Ohki

Research output: Contribution to journalArticlepeer-review

201 Citations (Scopus)

Abstract

The AML1-CBFβ transcription factor complex is the most frequent target of specific chromosome translocations in human leukemia. The MOZ gene, which encodes a histone acetyltransferase (HAT), is also involved in some leukemia-associated translocations. We report here that MOZ is part of the AML1 complex and strongly stimulates AML1-mediated transcription. The stimulation of AML1-mediated transcription is independent of the inherent HAT activity of MOZ. Rather, a potent transactivation domain within MOZ appears to be essential for stimulation of AML1-mediated transcription. MOZ, as well as CBP and MOZ - CBP, can acetylate AML1 in vitro. The amount of AML1 - MOZ complex increases during the differentiation of M1 myeloid cells into monocytes/macrophages, suggesting that the AML1 - MOZ complex might play a role in cell differentiation. On the other hand, the MOZ - CBP fusion protein, which is created by the t(8;16) translocation associated with acute monocytic leukemia, inhibits AML1-mediated transcription and differentiation of M1 cells. These results suggest that MOZ - CBP might induce leukemia by antagonizing the function of the AML1 complex.

Original languageEnglish
Pages (from-to)7184-7196
Number of pages13
JournalEMBO Journal
Volume20
Issue number24
DOIs
Publication statusPublished - 17-12-2001
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General Neuroscience
  • Molecular Biology
  • General Biochemistry,Genetics and Molecular Biology
  • General Immunology and Microbiology

Fingerprint

Dive into the research topics of 'Activation of AML1-mediated transcription by MOZ and inhibition by the MOZ-CBP fusion protein'. Together they form a unique fingerprint.

Cite this