scholarly journals Embryonic stem cells: protein interaction networks

2011 ◽  
Vol 2 (1-2) ◽  
pp. 13-25 ◽  
Author(s):  
Patricia Miang-Lon Ng ◽  
Thomas Lufkin

AbstractEmbryonic stem cells have the ability to differentiate into nearly all cell types. However, the molecular mechanism of its pluripotency is still unclear. Oct3/4, Sox2 and Nanog are important factors of pluripotency. Oct3/4 (hereafter referred to as Oct4), in particular, has been an irreplaceable factor in the induction of pluripotency in adult cells. Proteins interacting with Oct4 and Nanog have been identified via affinity purification and mass spectrometry. These data, together with iterative purifications of interacting proteins allowed a protein interaction network to be constructed. The network currently includes 77 transcription factors, all of which are interconnected in one network. In-depth studies of some of these transcription factors show that they all recruit the NuRD complex. Hence, transcription factor clustering and chromosomal remodeling are key mechanism used by embryonic stem cells. Studies using RNA interference suggest that more pluripotency genes are yet to be discovered via protein-protein interactions. More work is required to complete and curate the embryonic stem cell protein interaction network. Analysis of a saturated protein interaction network by system biology tools can greatly aid in the understanding of the embryonic stem cell pluripotency network.

2010 ◽  
Vol 6 (4) ◽  
pp. 369-381 ◽  
Author(s):  
Debbie L.C. van den Berg ◽  
Tim Snoek ◽  
Nick P. Mullin ◽  
Adam Yates ◽  
Karel Bezstarosti ◽  
...  

2016 ◽  
Vol 12 (4) ◽  
pp. 1324-1332 ◽  
Author(s):  
Leijie Li ◽  
Zhaobin Chen ◽  
Liangcai Zhang ◽  
Guiyou Liu ◽  
Jinlian Hua ◽  
...  

LMA: A novel model to predict target of pluripotency transcriptional factors in human embryonic stem cell.


Nature ◽  
2006 ◽  
Vol 444 (7117) ◽  
pp. 364-368 ◽  
Author(s):  
Jianlong Wang ◽  
Sridhar Rao ◽  
Jianlin Chu ◽  
Xiaohua Shen ◽  
Dana N. Levasseur ◽  
...  

2013 ◽  
Vol 9 (1) ◽  
pp. 694 ◽  
Author(s):  
Silvia Muñoz Descalzo ◽  
Pau Rué ◽  
Fernando Faunes ◽  
Penelope Hayward ◽  
Lars Martin Jakt ◽  
...  

Zygote ◽  
2021 ◽  
pp. 1-6
Author(s):  
Gerelchimeg Bou ◽  
Shimeng Guo ◽  
Jia Guo ◽  
Zhuang Chai ◽  
Jianchao Zhao ◽  
...  

Summary The efficiency of establishing pig pluripotent embryonic stem cell clones from blastocysts is still low. The transcription factor Nanog plays an important role in maintaining the pluripotency of mouse and human embryonic stem cells. Adequate activation of Nanog has been reported to increase the efficiency of establishing mouse embryonic stem cells from 3.5 day embryos. In mouse, Nanog starts to be strongly expressed as early as the morula stage, whereas in porcine NANOG starts to be strongly expressed by the late blastocyst stage. Therefore, here we investigated both the effect of expressing NANOG on porcine embryos early from the morula stage and the efficiency of porcine pluripotent embryonic stem cell clone formation. Compared with intact porcine embryos, NANOG overexpression induced a lower blastocyst rate, and did not show any advantages for embryo development and pluripotent embryonic stem cell line formation. These results indicated that, although NANOG is important pluripotent factor, NANOG overexpression is unnecessary for the initial formation of porcine pluripotent embryonic stem cell clones in vitro.


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