Lysine acetyltransferase Tip60 is required for hematopoietic stem cell maintenance

Author:

Numata Akihiko12ORCID,Kwok Hui Si1ORCID,Zhou Qi-Ling1ORCID,Li Jia1,Tirado-Magallanes Roberto1ORCID,Angarica Vladimir Espinosa1ORCID,Hannah Rebecca34ORCID,Park Jihye5,Wang Chelsia Qiuxia1,Krishnan Vaidehi1ORCID,Rajagopalan Deepa1ORCID,Zhang Yanzhou1ORCID,Zhou Siqin1,Welner Robert S.6,Osato Motomi1ORCID,Jha Sudhakar1ORCID,Bohlander Stefan K.7ORCID,Göttgens Berthold34ORCID,Yang Henry1,Benoukraf Touati18ORCID,Lough John W.9,Bararia Deepak110ORCID,Tenen Daniel G.110

Affiliation:

1. Cancer Science Institute of Singapore, National University of Singapore, Singapore;

2. Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan;

3. Department of Haematology, Wellcome and Medical Research Council Cambridge Stem Cell Institute, and

4. Cambridge Institute for Medical Research, Cambridge University, Cambridge, United Kingdom;

5. Department of Pathology, Beth Israel Deaconess Medical Center, Boston, MA;

6. Hematology Oncology, Department of Medicine, The University of Alabama at Birmingham Comprehensive Cancer Center, Birmingham, AL;

7. Leukaemia and Blood Cancer Research Unit, Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand;

8. Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St John’s, NL, Canada;

9. Department of Cell Biology, Neurobiology, and Anatomy, and the Cardiovascular Center, Medical College of Wisconsin, Milwaukee, WI; and

10. Harvard Stem Cell Institute, Harvard Medical School, Boston, MA

Abstract

Abstract Hematopoietic stem cells (HSCs) have the potential to replenish the blood system for the lifetime of the organism. Their 2 defining properties, self-renewal and differentiation, are tightly regulated by the epigenetic machineries. Using conditional gene-knockout models, we demonstrated a critical requirement of lysine acetyltransferase 5 (Kat5, also known as Tip60) for murine HSC maintenance in both the embryonic and adult stages, which depends on its acetyltransferase activity. Genome-wide chromatin and transcriptome profiling in murine hematopoietic stem and progenitor cells revealed that Tip60 colocalizes with c-Myc and that Tip60 deletion suppress the expression of Myc target genes, which are associated with critical biological processes for HSC maintenance, cell cycling, and DNA repair. Notably, acetylated H2A.Z (acH2A.Z) was enriched at the Tip60-bound active chromatin, and Tip60 deletion induced a robust reduction in the acH2A.Z/H2A.Z ratio. These results uncover a critical epigenetic regulatory layer for HSC maintenance, at least in part through Tip60-dependent H2A.Z acetylation to activate Myc target genes.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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