Histone acetyltransferase activity of MOF is required for adult but not early fetal hematopoiesis in mice Journal Article


Authors: Valerio, D. G.; Xu, H.; Eisold, M. E.; Woolthuis, C. M.; Pandita, T. K.; Armstrong, S. A.
Article Title: Histone acetyltransferase activity of MOF is required for adult but not early fetal hematopoiesis in mice
Abstract: K(lysine) acetyltransferase 8 (KAT8, also known as MOF) mediates the acetylation of histone H4 at lysine 16 (H4K16ac) and is crucial for murine embryogenesis. Lysine acetyltransferases have been shown to regulate various stages of normal hematopoiesis. However, the function of MOF in hematopoietic stem cell (HSC) development has not yet been elucidated. We set out to study the role of MOF in general hematopoiesis by using a Vav1-cre-induced conditional murine Mof knockout system and found that MOF is critical for hematopoietic cell maintenance and HSC engraftment capacity in adult hematopoiesis. Rescue experiments with a MOF histone acetyltransferase domain mutant illustrated the requirement for MOF acetyltransferase activity in the clonogenic capacity of HSCs and progenitors. In stark contrast, fetal steady-state hematopoiesis at embryonic day (E) 14.5 was not affected by homozygous Mof deletion despite dramatic loss of global H4K16ac. Hematopoietic defects start manifesting in late gestation at E17.5. The discovery that MOF and its H4K16ac activity are required for adult but not early and midgestational hematopoiesis supports the notion that multiple chromatin regulators may be crucial for hematopoiesis at varying stages of development. MOF is therefore a developmental-stage-specific chromatin regulator found to be essential for adult but not early fetal hematopoiesis. © 2017 by The American Society of Hematology.
Journal Title: Blood
Volume: 129
Issue: 1
ISSN: 0006-4971
Publisher: American Society of Hematology  
Date Published: 2017-01-05
Start Page: 48
End Page: 59
Language: English
DOI: 10.1182/blood-2016-05-714568
PROVIDER: scopus
PMCID: PMC5216264
PUBMED: 27827827
DOI/URL:
Notes: Article -- Export Date: 3 April 2017 -- Source: Scopus
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MSK Authors
  1. Haiming Xu
    18 Xu
  2. Scott Allen Armstrong
    108 Armstrong
  3. Meghan Elizabeth Eisold
    3 Eisold