| Literature DB >> 27471261 |
Shin Kobayashi1, Yusuke Hosoi2, Hirosuke Shiura2, Kazuo Yamagata3, Saori Takahashi2, Yoshitaka Fujihara3, Takashi Kohda2, Masaru Okabe3, Fumitoshi Ishino2.
Abstract
Pluripotent stem cells can be classified into two distinct states, naïve and primed, which show different degrees of potency. One difficulty in stem cell research is the inability to distinguish these states in live cells. Studies on female mice have shown that reactivation of inactive X chromosomes occurs in the naïve state, while one of the X chromosomes is inactivated in the primed state. Therefore, we aimed to distinguish the two states by monitoring X chromosome reactivation. Thus far, X chromosome reactivation has been analysed using fixed cells; here, we inserted different fluorescent reporter gene cassettes (mCherry and eGFP) into each X chromosome. Using these knock-in 'Momiji' mice, we detected X chromosome reactivation accurately in live embryos, and confirmed that the pluripotent states of embryos were stable ex vivo, as represented by embryonic and epiblast stem cells in terms of X chromosome reactivation. Thus, Momiji mice provide a simple and accurate method for identifying stem cell status based on X chromosome reactivation.Entities:
Keywords: Early mouse development; Live-cell imaging; Pluripotent stem cells; X chromosome inactivation; X chromosome reactivation
Mesh:
Substances:
Year: 2016 PMID: 27471261 DOI: 10.1242/dev.136739
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868