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Species-Specific Enhancer Activity of OCT4 in Porcine Pluripotency: The Porcine Reporter System Could Monitor Pluripotency in Porcine Embryo Development and Embryonic Stem Cells

Overview
Journal Stem Cells Int
Publisher Wiley
Specialty Cell Biology
Date 2022 Jul 18
PMID 35846983
Authors
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Abstract

The present study examined the activity and function of the pig enhancer in the porcine early embryonic development stage and porcine authentic embryonic stem cells. OCT4 is known as a pluripotent regulator, and its upstream regulatory region-based dual-fluorescence protein reporter system controlled by distal and proximal enhancers is broadly used in studies examining the states and mechanism of pluripotency. We analyzed how this reporter system functions during early embryo development and in stem cells using a previously established porcine-specific reporter system. We demonstrated that the porcine distal enhancer and proximal enhancer were activated with different expression patterns simultaneously as the expression of pluripotent marker genes changed during the development of in vitro pathenotes and the establishment of porcine embryonic stem cells (ESCs). This work demonstrates the applicability of the porcine upstream region-derived dual-fluorescence reporter system, which may be applied to investigations of species-specific pluripotency in porcine-origin cells. These reporter systems may be useful tools for studies of porcine-specific pluripotency, early embryo development, and embryonic stem cells.

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References
1.
Theunissen T, Powell B, Wang H, Mitalipova M, Faddah D, Reddy J . Systematic Identification of Culture Conditions for Induction and Maintenance of Naive Human Pluripotency. Cell Stem Cell. 2017; 15(4):524-526. PMC: 4534765. DOI: 10.1016/j.stem.2014.09.003. View

2.
Bulger M, Groudine M . Functional and mechanistic diversity of distal transcription enhancers. Cell. 2011; 144(3):327-39. PMC: 3742076. DOI: 10.1016/j.cell.2011.01.024. View

3.
Kim S, Choi K, Lee D, Lee M, Hwang J, Lee C . Identification and Characterization of the Upstream Regulatory Region in . Stem Cells Int. 2019; 2019:2130973. PMC: 6434273. DOI: 10.1155/2019/2130973. View

4.
Choi K, Lee D, Kim S, Woo S, Kim D, Lee C . Chemically Defined Media Can Maintain Pig Pluripotency Network In Vitro. Stem Cell Reports. 2019; 13(1):221-234. PMC: 6626979. DOI: 10.1016/j.stemcr.2019.05.028. View

5.
Nakagawa M, Koyanagi M, Tanabe K, Takahashi K, Ichisaka T, Aoi T . Generation of induced pluripotent stem cells without Myc from mouse and human fibroblasts. Nat Biotechnol. 2007; 26(1):101-6. DOI: 10.1038/nbt1374. View