Details

Autor(en) / Beteiligte

• Yamaguchi, Yukari
• Takamura, Hiroyuki
• Tada, Yuhki
• Akagi, Tadayuki
• Oyama, Katsunobu
• Miyashita, Tomoharu
• Tajima, Hidehiro
• Kitagawa, Hirohisa
• Fushida, Sachio
• Yokota, Takashi
• Ohta, Tetsuo
• Koide, Hiroshi

Titel

Nanog positively regulates Zfp57 expression in mouse embryonic stem cells

Ist Teil von

• Biochemical and biophysical research communications, 2014-10, Vol.453 (4), p.817-820

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2014

Quelle

Elsevier ScienceDirect Journals

Beschreibungen/Notizen

• •Nanog positively regulates Zfp57 expression in ES cells.•The Nanog/Zfp57 pathway promotes anchorage-independent growth of ES cells.•NANOG overexpression results in upregulation of ZFP57 in cancer cells. To maintain the self-renewal of embryonic stem (ES) cells, several core transcription factors, including Oct3/4, STAT3, and Nanog, regulate the expression of their target genes. Zinc finger protein 57 (Zfp57) is specifically expressed in self-renewing ES cells and its expression level is reduced upon ES cell differentiation, suggesting that expression of this transcription factor is regulated by core transcription factors. In the present study, we investigated whether Zfp57 expression is regulated by Nanog. Nanog overexpression resulted in the upregulation of Zfp57. On the other hand, knockdown of Nanog reduced the expression level of Zfp57. In addition, we identified the Nanog-responsive region in the promoter of the Zfp57 gene. These results suggest that Nanog is an upstream regulator of Zfp57. Moreover, Nanog overexpression promoted the growth of ES cells in soft agar and this was suppressed by Zfp57 knockdown, suggesting that the Nanog/Zfp57 pathway plays a central role in anchorage-independent growth of ES cells. Interestingly, NANOG overexpression also led to the upregulation of ZFP57 in two human tumor cell lines. Taken together, our results suggest that Nanog positively regulates Zfp57 expression in multiple types of cells.