Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5505840 | Biochemical and Biophysical Research Communications | 2017 | 29 Pages |
Abstract
We demonstrated that ETV4 is a transcriptional activator of the NANOG gene in human embryonic carcinoma NCCIT cells. The endogenous expression of NANOG and ETV4 in naïve cells was significantly down-regulated upon differentiation and by shRNA-mediated knockdown of ETV4. NANOG transcription was significantly upregulated by ETV4 overexpression. A putative ETS binding site (EBS) is present in the region (â285 to â138) of the proximal promoter. Site-directed mutagenesis of the putative EBS (â196AGGATTâ191) abolished NANOG promoter activity and ETV4 interacted with this putative EBS both in vivo and in vitro. Our data provide the molecular details of ETV4-mediated NANOG gene expression.
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Authors
Sung-Won Park, Hyun-Jin Do, Wonbin Choi, Hyuk Song, Hak-Jae Chung, Jae-Hwan Kim,