Format

Send to

Choose Destination
See comment in PubMed Commons below
Cell Stem Cell. 2014 Sep 4;15(3):281-294. doi: 10.1016/j.stem.2014.06.004.

Histone variant H2A.X deposition pattern serves as a functional epigenetic mark for distinguishing the developmental potentials of iPSCs.

Author information

1
Yale Stem Cell Center and Department of Genetics, Yale School of Medicine, New Haven, CT 06520, USA.
2
Ronald O. Perelman and Claudia Cohen Center for Reproductive Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
3
Yale Stem Cell Center and Department of Cell Biology, Yale School of Medicine, New Haven, CT 06520, USA.
4
Massachusetts General Hospital Cancer Center, Howard Hughes Medical Institute and Department of Stem Cell and Regenerative Medicine, Harvard University, Boston, MA 02114, USA.
5
Yale Stem Cell Center and Department of Genetics, Yale School of Medicine, New Haven, CT 06520, USA. Electronic address: andrew.xiao@yale.edu.

Abstract

For future application of induced pluripotent stem cell (iPSC) technology, the ability to assess the overall quality of iPSC clones will be an important issue. Here we show that the histone variant H2A.X is a functional marker that can distinguish the developmental potentials of mouse iPSC lines. We found that H2A.X is specifically targeted to and negatively regulates extraembryonic lineage gene expression in embryonic stem cells (ESCs) and prevents trophectoderm lineage differentiation. ESC-specific H2A.X deposition patterns are faithfully recapitulated in iPSCs that support the development of "all-iPS" animals via tetraploid complementation, the most stringent test available of iPSC quality. In contrast, iPSCs that fail to support all-iPS embryonic development show aberrant H2A.X deposition, upregulation of extraembryonic lineage genes, and a predisposition to extraembryonic differentiation. Thus, our work has highlighted an epigenetic mechanism for maintaining cell lineage commitment in ESCs and iPSCs that can be used to distinguish the quality of iPSC lines.

PMID:
25192463
DOI:
10.1016/j.stem.2014.06.004
[Indexed for MEDLINE]
Free full text
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Elsevier Science
    Loading ...
    Support Center