scholarly journals Enhanced generation of human embryonic stem cells from single blastomeres of fair and poor-quality cleavage embryos via inhibition of glycogen synthase kinase β and Rho-associated kinase signaling

2013 ◽  
Vol 28 (10) ◽  
pp. 2661-2671 ◽  
Author(s):  
Adeleh Taei ◽  
Seyedeh-Nafiseh Hassani ◽  
Poopak Eftekhari-Yazdi ◽  
Mojtaba Rezazadeh Valojerdi ◽  
Mohsen Nokhbatolfoghahai ◽  
...  
Stem Cells ◽  
2007 ◽  
Vol 25 (11) ◽  
pp. 2705-2711 ◽  
Author(s):  
Hiroki Umehara ◽  
Tohru Kimura ◽  
Satoshi Ohtsuka ◽  
Toshinobu Nakamura ◽  
Kenji Kitajima ◽  
...  

2007 ◽  
Vol 2 (8) ◽  
pp. 1963-1972 ◽  
Author(s):  
Irina Klimanskaya ◽  
Young Chung ◽  
Sandy Becker ◽  
Shi-Jiang Lu ◽  
Robert Lanza

2009 ◽  
Vol 24 (8) ◽  
pp. 1844-1851 ◽  
Author(s):  
J.L. Cortes ◽  
L. Sanchez ◽  
G. Ligero ◽  
I. Gutierrez-Aranda ◽  
P. Catalina ◽  
...  

2018 ◽  
Vol 293 (27) ◽  
pp. 10731-10743 ◽  
Author(s):  
Kelsie J. Faulds ◽  
Jennifer N. Egelston ◽  
Laura J. Sedivy ◽  
Matthew K. Mitchell ◽  
Sanjana Garimella ◽  
...  

2015 ◽  
Vol 26 (11) ◽  
pp. 2139-2150 ◽  
Author(s):  
Gavin D. Meredith ◽  
Anthony D'Ippolito ◽  
Miroslav Dudas ◽  
Leigh C. Zeidner ◽  
Logan Hostetter ◽  
...  

Glycogen synthase kinase-3 (Gsk-3) is a key regulator of multiple signal transduction pathways. Recently we described a novel role for Gsk-3 in the regulation of DNA methylation at imprinted loci in mouse embryonic stem cells (ESCs), suggesting that epigenetic changes regulated by Gsk-3 are likely an unrecognized facet of Gsk-3 signaling. Here we extend our initial observation to the entire mouse genome by enriching for methylated DNA with the MethylMiner kit and performing next-generation sequencing (MBD-Seq) in wild-type and Gsk-3α−/−;Gsk-3β−/− ESCs. Consistent with our previous data, we found that 77% of known imprinted loci have reduced DNA methylation in Gsk-3-deficient ESCs. More specifically, we unambiguously identified changes in DNA methylation within regions that have been confirmed to function as imprinting control regions. In many cases, the reduced DNA methylation at imprinted loci in Gsk-3α−/−;Gsk-3β−/− ESCs was accompanied by changes in gene expression as well. Furthermore, many of the Gsk-3–dependent, differentially methylated regions (DMRs) are identical to the DMRs recently identified in uniparental ESCs. Our data demonstrate the importance of Gsk-3 activity in the maintenance of DNA methylation at a majority of the imprinted loci in ESCs and emphasize the importance of Gsk-3–mediated signal transduction in the epigenome.


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