TY - JOUR
T1 - Identification of a novel enhancer of CEBPE essential for granulocytic differentiation
AU - Shyamsunder, Pavithra
AU - Shanmugasundaram, Mahalakshmi
AU - Mayakonda, Anand
AU - Dakle, Pushkar
AU - Teoh, Weoi Woon
AU - Han, Lin
AU - Kanojia, Deepika
AU - Lim, Mei Chee
AU - Fullwood, Melissa
AU - An, Omer
AU - Yang, Henry
AU - Shi, Jizhong
AU - Hossain, Mohammad Zakir
AU - Madan, Vikas
AU - Koeffler, H. Phillip
N1 - Funding Information:
This work was supported by the Leukemia Lymphoma Society of America, the Singapore Ministry of Health’s National Medical Research Council (NMRC) under its Singapore Translational Research (STaR) Investigator Award (NMRC/STaR/0021/2014, H.P.K.), Singapore Ministry of Education Academic Research Fund Tier 2 (MOE2013-T2-2-150), an NMRC Centre Grant awarded to National University Cancer Institute of Singapore (NMRC/CG/012/2013), and the National Research Foundation Singapore and the Singapore Ministry of Education under its Research Centres of Excellence initiatives. This work was also supported by the RNA Biology Centre at the Cancer Science Institute of Singapore, NUS, as part of funding under the Singapore Ministry of Education’s Tier 3 grants (grant MOE2014-T3-1-006).
PY - 2019/6/6
Y1 - 2019/6/6
N2 - CCAAT/enhancer binding protein (CEBPE) is an essential transcription factor for granulocytic differentiation. Mutations of CEBPE occur 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 Cebpe in murine myeloid cells.We identified an interaction between this 16-kb region and the core promoter of Cebpe using 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 16-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 the16-kb enhancer resulted in reduced levels of CEBPE and its target genes and caused a severe block in granulocytic differentiation.Wealso identified binding of CEBPAand CEBPE to the16-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 Cebpe and required for normal granulocytic differentiation.
AB - CCAAT/enhancer binding protein (CEBPE) is an essential transcription factor for granulocytic differentiation. Mutations of CEBPE occur 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 Cebpe in murine myeloid cells.We identified an interaction between this 16-kb region and the core promoter of Cebpe using 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 16-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 the16-kb enhancer resulted in reduced levels of CEBPE and its target genes and caused a severe block in granulocytic differentiation.Wealso identified binding of CEBPAand CEBPE to the16-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 Cebpe and required for normal granulocytic differentiation.
UR - http://www.scopus.com/inward/record.url?scp=85067342160&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85067342160&partnerID=8YFLogxK
U2 - 10.1182/blood.2018886077
DO - 10.1182/blood.2018886077
M3 - Article
C2 - 30952671
AN - SCOPUS:85067342160
SN - 0006-4971
VL - 133
SP - 2507
EP - 2517
JO - Blood
JF - Blood
IS - 23
ER -