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Identification of a novel enhancer of CEBPE essential for granulocytic differentiation.
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.
Afiliação
  • Shyamsunder P; Cancer Science Institute of Singapore and.
  • Shanmugasundaram M; Cancer Science Institute of Singapore and.
  • Mayakonda A; Cancer Science Institute of Singapore and.
  • Dakle P; Cancer Science Institute of Singapore and.
  • Teoh WW; Cancer Science Institute of Singapore and.
  • Han L; Cancer Science Institute of Singapore and.
  • Kanojia D; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
  • Lim MC; Cancer Science Institute of Singapore and.
  • Fullwood M; Cancer Science Institute of Singapore and.
  • An O; Cancer Science Institute of Singapore and.
  • Yang H; Cancer Science Institute of Singapore and.
  • Shi J; Cancer Science Institute of Singapore and.
  • Hossain MZ; Cancer Science Institute of Singapore and.
  • Madan V; Cancer Science Institute of Singapore and.
  • Koeffler HP; Cancer Science Institute of Singapore and.
Blood ; 133(23): 2507-2517, 2019 06 06.
Article em En | MEDLINE | ID: mdl-30952671
CCAAT/enhancer binding protein ε (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 +6-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 +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 Cebpe and required for normal granulocytic differentiation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diferenciação Celular / Regulação da Expressão Gênica / Proteínas Estimuladoras de Ligação a CCAAT / Mielopoese / Granulócitos Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diferenciação Celular / Regulação da Expressão Gênica / Proteínas Estimuladoras de Ligação a CCAAT / Mielopoese / Granulócitos Idioma: En Ano de publicação: 2019 Tipo de documento: Article