Association of DDX5/p68 protein with the upstream erythroid enhancer element (EHS1) of the gene encoding the KLF1 transcription factor

被引:0
|
作者
Chen, Xiaoyong [1 ,5 ,6 ]
Pillay, Sanjana [1 ]
Lohmann, Felix [1 ]
Bieker, James J. [1 ,2 ,3 ,4 ]
机构
[1] Mt Sinai Sch Med, Dept Cell Dev & Regenerat Biol, New York, NY 10029 USA
[2] Mt Sinai Sch Med, Black Familly Stem Cell Inst, New York, NY 10029 USA
[3] Mt Sinai Sch Med, Tish Canc Inst, New York, NY 10029 USA
[4] Mt Sinai Sch Med, Mindich Child Hlth & Dev Inst, New York, NY 10029 USA
[5] Yale Univ, Dept Pediat, Sch Med, New Haven, CT USA
[6] Novartis Inst Biomed Res, Basel, Switzerland
关键词
KRUPPEL-LIKE FACTOR; HEMATOPOIETIC STEM-CELLS; BOX-GATA MOTIF; BINDING-PROTEIN; RNA HELICASES; EKLF GENE; EXPRESSION; CTCF; P68; IDENTIFICATION;
D O I
10.1016/j.jbc.2023.105489
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
EKLF/KLF1 is an essential transcription factor that plays a global role in erythroid transcriptional activation. Regulation of KLF1 is of interest, as it displays a highly restricted expression pattern, limited to erythroid cells and its progenitors. Here we use biochemical affinity purification to identify the DDX5/p68 protein as an activator of KLF1 by virtue of its interaction with the erythroid-specific DNAse hypersensitive site upstream enhancer element (EHS1). We further show that this protein associates with DEK and CTCF. We postulate that the range of interactions of DDX5/p68 with these and other proteins known to interact with this element render it part of the enhanseosome complex critical for optimal expression of KLF1 and enables the formation of a proper chromatin configuration at the Klf1 locus. These individual interactions provide quantitative contributions that, in sum, establish the high-level activity of the Klf1 promoter and suggest they can be selectively manipulated for clinical benefit.
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页数:8
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