| Literature DB >> 22770243 |
Kiichiro Tomoda1, Kazutoshi Takahashi, Karen Leung, Aki Okada, Megumi Narita, N Alice Yamada, Kirsten E Eilertson, Peter Tsang, Shiro Baba, Mark P White, Salma Sami, Deepak Srivastava, Bruce R Conklin, Barbara Panning, Shinya Yamanaka.
Abstract
Female human induced pluripotent stem cell (hiPSC) lines exhibit variability in X-inactivation status. The majority of hiPSC lines maintain one transcriptionally active X (Xa) and one inactive X (Xi) chromosome from donor cells. However, at low frequency, hiPSC lines with two Xas are produced, suggesting that epigenetic alterations of the Xi occur sporadically during reprogramming. We show here that X-inactivation status in female hiPSC lines depends on derivation conditions. hiPSC lines generated by the Kyoto method (retroviral or episomal reprogramming), which uses leukemia inhibitory factor (LIF)-expressing SNL feeders, frequently had two Xas. Early passage Xa/Xi hiPSC lines generated on non-SNL feeders were converted into Xa/Xa hiPSC lines after several passages on SNL feeders, and supplementation with recombinant LIF caused reactivation of some of X-linked genes. Thus, feeders are a significant factor affecting X-inactivation status. The efficient production of Xa/Xa hiPSC lines provides unprecedented opportunities to understand human X-reactivation and -inactivation.Entities:
Mesh:
Year: 2012 PMID: 22770243 PMCID: PMC3396435 DOI: 10.1016/j.stem.2012.05.019
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633