Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Since the discovery of induced pluripotent stem cells there has been intense interest in understanding the mechanisms that allow a somatic cell to be reprogrammed back to a pluripotent state. Several groups have studied the alterations in gene expression that occur as somatic cells modify their genome to that of an embryonic stem cell. Underpinning many of the gene expression changes are modifications to the epigenetic profile of the associated chromatin. We have used a large-scale shRNA screen to identify epigenetic modifiers that act as barriers to reprogramming. We have uncovered an important role for TRIM28 in cells resisting transition between somatic and pluripotent states. TRIM28 achieves this by maintaining the H3K9me3 repressed state and keeping endogenous retroviruses (ERVs) silenced. We propose that knockdown of TRIM28 during reprogramming results in more plastic H3K9me3 domains, dysregulation of genes nearby H3K9me3 marks, and up regulation of ERVs, thus facilitating the transition through reprogramming. Stem Cells 2017;35:147-157.

More information Original publication

DOI

10.1002/stem.2453

Type

Journal article

Publication Date

2017-01-01T00:00:00+00:00

Volume

35

Pages

147 - 157

Total pages

10

Keywords

Epigenetics, Induced pluripotent stem cells, Reprogramming, Trim28, Animals, Cell Proliferation, Cellular Reprogramming, Chromatin, Endogenous Retroviruses, Epigenesis, Genetic, Gene Knockdown Techniques, Histone-Lysine N-Methyltransferase, Histones, Lysine, Methylation, Mice, Transgenic, Models, Biological, Pluripotent Stem Cells, RNA, Small Interfering, Tripartite Motif-Containing Protein 28, Up-Regulation