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Differential transcriptional regulation of the NANOG gene in chicken primordial germ cells and embryonic stem cells

Authors :
Hee Jung Choi
Jae Yong Han
Deivendran Rengaraj
Bertrand Pain
Jin Hwa Kim
So Dam Jin
Seoul National University [Seoul] (SNU)
Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
Institut cellule souche et cerveau (U846 Inserm - UCBL1)
Institut National de la Recherche Agronomique (INRA)-Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)
Shinshu University [Nagano]
This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) [2015R1A3A2033826] and [2018R1D1A1B07049376]
Girard, Agnès
Source :
Journal of Animal Science and Biotechnology, Journal of Animal Science and Biotechnology, BioMed Central, 2021, 12 (1), ⟨10.1186/s40104-021-00563-5⟩, Journal of Animal Science and Biotechnology, Vol 12, Iss 1, Pp 1-14 (2021)
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

Background NANOG is a core transcription factor (TF) in embryonic stem cells (ESCs) and primordial germ cells (PGCs). Regulation of the NANOG gene by TFs, epigenetic factors, and autoregulatory factors is well characterized in ESCs, and transcriptional regulation of NANOG is well established in these cells. Although NANOG plays a key role in germ cells, the molecular mechanism underlying its transcriptional regulation in PGCs has not been studied. Therefore, we investigated the mechanism that regulates transcription of the chicken NANOG (cNANOG) gene in PGCs and ESCs. Results We first identified the transcription start site of cNANOG by 5′-rapid amplification of cDNA ends PCR analysis. Then, we measured the promoter activity of various 5′ flanking regions of cNANOG in chicken PGCs and ESCs using the luciferase reporter assay. cNANOG expression required transcriptional regulatory elements, which were positively regulated by POU5F3 (OCT4) and SOX2 and negatively regulated by TP53 in PGCs. The proximal region of the cNANOG promoter contains a positive transcriptional regulatory element (CCAAT/enhancer-binding protein (CEBP)-binding site) in ESCs. Furthermore, small interfering RNA-mediated knockdown demonstrated that POU5F3, SOX2, and CEBP played a role in cell type-specific transcription of cNANOG. Conclusions We show for the first time that different trans-regulatory elements control transcription of cNANOG in a cell type-specific manner. This finding might help to elucidate the mechanism that regulates cNANOG expression in PGCs and ESCs.

Details

ISSN :
20491891 and 16749782
Volume :
12
Database :
OpenAIRE
Journal :
Journal of Animal Science and Biotechnology
Accession number :
edsair.doi.dedup.....686578cd511c6f3e864a5a3bb3445a6b