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PMID: 17823307 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Runx1-mediated hematopoietic stem-cell emergence is controlled by a Gata/Ets/SCL-regulated enhancer.

Blood ·Vol. 110 ·No. 13 ·2007-12-15 ·Pages 4188-97

Nottingham WT, Jarratt A, Burgess M, Speck CL, Cheng JF, Prabhakar S, Rubin EM, Li PS, Sloane-Stanley J, Kong-A-San J, de Bruijn MF

Abstract

The transcription factor Runx1/AML1 is an important regulator of hematopoiesis and is critically required for the generation of the first definitive hematopoietic stem cells (HSCs) in the major vasculature of the mouse embryo. As a pivotal factor in HSC ontogeny, its transcriptional regulation is of high interest but is largely undefined. In this study, we used a combination of comparative genomics and chromatin analysis to identify a highly conserved 531-bp enhancer located at position + 23.5 in the first intron of the 224-kb mouse Runx1 gene. We show that this enhancer contributes to the early hematopoietic expression of Runx1. Transcription factor binding in vivo and analysis of the mutated enhancer in transient transgenic mouse embryos implicate Gata2 and Ets proteins as critical factors for its function. We also show that the SCL/Lmo2/Ldb-1 complex is recruited to the enhancer in vivo. Importantly, transplantation experiments demonstrate that the intronic Runx1 enhancer targets all definitive HSCs in the mouse embryo, suggesting that it functions as a crucial cis-regulatory element that integrates the Gata, Ets, and SCL transcriptional networks to initiate HSC generation.

MeSH Terms
Adaptor Proteins, Signal Transducing Animals Basic Helix-Loop-Helix Transcription Factors/metabolism,physiology Core Binding Factor Alpha 2 Subunit/genetics,physiology DNA-Binding Proteins/metabolism Embryo, Mammalian Enhancer Elements, Genetic/physiology GATA2 Transcription Factor/metabolism,physiology Hematopoietic Stem Cells/cytology LIM Domain Proteins Metalloproteins/metabolism Mice Multiprotein Complexes/metabolism Proto-Oncogene Protein c-ets-1/metabolism,physiology Proto-Oncogene Proteins/metabolism,physiology T-Cell Acute Lymphocytic Leukemia Protein 1 Transcription, Genetic
Chemicals
Adaptor Proteins, Signal Transducing Basic Helix-Loop-Helix Transcription Factors Core Binding Factor Alpha 2 Subunit DNA-Binding Proteins GATA2 Transcription Factor LIM Domain Proteins Ldb1 protein, mouse Lmo2 protein, mouse Metalloproteins Multiprotein Complexes Proto-Oncogene Protein c-ets-1 Proto-Oncogene Proteins Runx1 protein, mouse T-Cell Acute Lymphocytic Leukemia Protein 1 Tal1 protein, mouse
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Nottingham Wade T
Medical Research Council (MRC) Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, UK.
Jarratt Andrew
Burgess Matthew
Speck Caroline L
Cheng Jan-Fang
Prabhakar Shyam
Rubin Eddy M
Li Pik-Shan
Sloane-Stanley Jackie
Kong-A-San John
de Bruijn Marella F T R
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Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2007-12-15
Epub
2007-00-06
Pages
4188-97
Language
English
Region
United States
NLM ID
7603509
PMCID
PMC2234795
Subset
IM
Grants
Medical Research Council · MC_U137970202 · United Kingdom
NHLBI NIH HHS · U01 HL066681 · United States
NHLBI NIH HHS · HL066681 · United States
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