Mitochondria and cytosol were isolated using a Mitochondria/ Cytosol fractionation kit

f Lentiviral Transduction in Pig Pluripotent Cells transgenes during differentiations. The differences of our results with previous porcine studies may be as a result of the different vector construct and transfection method used. The reactivation of silenced transgenes during differentiation that we observed in this study indicate that trans-acting factors, as well as DNA methylations, affect transgene silencing in undifferentiated EpiSC-like pESCs. When transduced cells were treated with 5-AzadC and TSA, inhibitors of DNA methylation and histone deacetylases, respectively, 5-AzadC allowed reactivation of silenced expression, but TSA did not. Bisulfite sequencing of the promoter regions showed that 5-AzadC-treated samples were hypomethylated in CMV promoter regions compared with the other treated groups, which had hypermethylated promoters. These results clearly demonstrate that decreased transgene expression is related to DNA methylation in promoter regions, not histone 606143-89-9 modifications. In addition to silencing of gene expression during extended culture, the transfection efficiency of EpiSC-like pESCs was lower than that of other embryo-originated somatic cells. However, PSIP1, a protein that participates in lentiviral provirus integration into host genomes, was 10646850 examined by RT-PCR and no difference was observed among EpiSC-like pESCs, PEFs, and MEFs. This result suggests that the low efficiency of transfection is not related to the low integrity of the provirus. In addition, because the copy number of an inserted lentiviral construct could affect EGFP expression, a correlation between EGFP expression level and transgene copy number was verified. However, because of heterogeneity in the transduced cells due to the random insertion of multiple copies, it is hard to quantitatively measure the copy number of inserted transgenes. So, transgene copy number was relatively quantified by real-time RCR. Realtime PCR results showed that changes in EGFP expression and transgene copy number are not correlated. And also reactivation of silenced transgenes during differentiation clearly demonstrated that low expression levels are not due to low integrity. Note that DNA methylation levels of the CMV promoter region did not change during differentiation although transgene expression increased. Undifferentiated and differentiated cells at the same passage have similar levels of DNA methylation in the CMV promoter. This suggests that the recruitment of transcription factors in differentiated cells or the downregulation of repressive trans-acting factors, rather than demethylation of the promoter region, is involved in the unmethylated open chromatin for reactivation of silenced transgenes. In fact, many binding sites for putative transacting factors such as cyclic AMP-response elements, NF-Kappa B, AP-1, serum response elements exist in the CMV promoter. These sites could be predicted by the program TFSEARCH ver. 1.3. This mechanism is supported by the phenomenon that more methylated cells in late passages showed 8402633 lower reactivation of transgenes. Therefore, low transgene expression in pluripotent cells is likely because of trans-acting factors as well as DNA methylation. In conclusion, we were able to successfully derive EpiSC-like pESCs and introduced an EGFP transgene into these cells using lentiviral vectors. Transgene expression in EpiSC-like pESCs was altered during maintenance and differentiation due to epigenetic changes. Although we used modified