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Identification of a novel enhancer of CEBPE essential for granulocytic differentiation

Authors :
Shyamsunder, Pavithra
Shanmugasundaram, Mahalakshmi
Mayakonda, Anand
Dakle, Pushkar
Teoh, Weoi Woon
Han, Lin
Kanojia, Deepika
Lim, Mei Chee
Fullwood, Melissa
An, Omer
Yang, Henry
Shi, Jizhong
Hossain, Mohammad Zakir
Madan, Vikas
Koeffler, H. Phillip
Source :
Blood; June 2019, Vol. 133 Issue: 23 p2507-2517, 11p
Publication Year :
2019

Abstract

CCAAT/enhancer binding protein ε (CEBPE) is an essential transcription factor for granulocytic differentiation. Mutations of CEBPEoccur in individuals with neutrophil-specific granule deficiency (SGD), which is characterized by defects in neutrophil maturation. Cebpe-knockout mice also exhibit defects in terminal differentiation of granulocytes, a phenotype reminiscent of SGD. Analysis of DNase I hypersensitive sites sequencing data revealed an open chromatin region 6 kb downstream of the transcriptional start site of Cebpein murine myeloid cells. We identified an interaction between this +6-kb region and the core promoter of Cebpeusing circular chromosome conformation capture sequencing (4C-seq). To understand the role of this putative enhancer in transcriptional regulation of Cebpe, we targeted it using catalytically inactive Cas9 fused to Krüppel-associated box (KRAB) domain and observed a significant downregulation of transcript and protein levels of CEBPE in cells expressing guide RNA targeting the +6-kb region. To further investigate the role of this novel enhancer further in myelopoiesis, we generated mice with deletion of this region using CRISPR/Cas9 technology. Germline deletion of the +6-kb enhancer resulted in reduced levels of CEBPE and its target genes and caused a severe block in granulocytic differentiation. We also identified binding of CEBPA and CEBPE to the +6-kb enhancer, which suggests their role in regulating the expression of Cebpe. In summary, we have identified a novel enhancer crucial for regulating expression of Cebpeand required for normal granulocytic differentiation.

Details

Language :
English
ISSN :
00064971 and 15280020
Volume :
133
Issue :
23
Database :
Supplemental Index
Journal :
Blood
Publication Type :
Periodical
Accession number :
ejs57039534
Full Text :
https://doi.org/10.1182/blood.2018886077