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GFI1 proteins orchestrate the emergence of haematopoietic stem cells through recruitment of LSD1

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posted on 2019-02-21, 09:42 authored by R Thambyrajah, M Mazan, R Patel, V Moignard, M Stefanska, E Marinopoulou, Y Li, C Lancrin, T Clapes, T Möröy, C Robin, C Miller, S Cowley, B Göttgens, V Kouskoff, G Lacaud
In vertebrates, the first haematopoietic stem cells (HSCs) with multi-lineage and long-term repopulating potential arise in the AGM (aorta-gonad-mesonephros) region. These HSCs are generated from a rare and transient subset of endothelial cells, called haemogenic endothelium (HE), through an endothelial-to-haematopoietic transition (EHT). Here, we establish the absolute requirement of the transcriptional repressors GFI1 and GFI1B (growth factor independence 1 and 1B) in this unique trans-differentiation process. We first demonstrate that Gfi1 expression specifically defines the rare population of HE that generates emerging HSCs. We further establish that in the absence of GFI1 proteins, HSCs and haematopoietic progenitor cells are not produced in the AGM, revealing the critical requirement for GFI1 proteins in intra-embryonic EHT. Finally, we demonstrate that GFI1 proteins recruit the chromatin-modifying protein LSD1, a member of the CoREST repressive complex, to epigenetically silence the endothelial program in HE and allow the emergence of blood cells.

Funding

Work in the laboratory is supported by the Leukaemia and Lymphoma Research Foundation (LLR), Cancer Research UK (CRUK) and the Biotechnology and Biological Sciences Research Council (BBSRC). S.C. is the recipient of an MRC senior fellowship (MR/J009202/1).

History

Citation

Nat Cell Biol, 2016, 18 (1), pp. 21-32

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/Biological Sciences/Molecular & Cell Biology

Version

  • AM (Accepted Manuscript)

Published in

Nat Cell Biol

Publisher

Nature Research

eissn

1476-4679

Acceptance date

2015-10-26

Copyright date

2015

Available date

2019-02-21

Publisher version

https://www.nature.com/articles/ncb3276

Language

en

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