Repository logo
 

Activation of lineage-regulators and transposable elements across a pluripotent spectrum

Published version
Peer-reviewed

Type

Article

Change log

Authors

Hackett, JA 
Kobayashi, T 
Dietmann, S 
Surani, MA 

Abstract

Embryonic stem cells (ESC) are characterised by the pluripotent capacity to generate all embryonic lineages. Here we show ESC can occupy a spectrum of distinct transcriptional and epigenetic states in response to varied extrinsic conditions. This spectrum broadly corresponds to a developmental continuum of pluripotency and is coupled with a gradient of increasing global DNA methylation. Each pluripotent state is linked with activation of distinct classes of transposable elements (TE), which in turn influence ESC through generating chimeric transcripts. Moreover, varied ESC culture parameters differentially license heterogeneous activation of master lineageregulators, including Sox1, Gata4 or Blimp1, and influence differentiation. Activation of Blimp1 is prevalent in 2i (without-LIF) conditions, and marks a dynamic primordial germ cell (PGC)-like sub-state, that is directly repressed by Klf4 downstream of LIF/STAT3 signalling. Thus, extrinsic cues establish a spectrum of pluripotent states, in part by modulating sub-populations, as well as directing the transcriptome, epigenome, and TE.

Description

Keywords

DNA methylation, KLF4, PGC, STAT3, chimeric transcripts, embryonic stem cell, heterogeneity, imprints, pluripotency, transposable element, Animals, CRISPR-Cas Systems, Cell Differentiation, Cell Line, Cell Lineage, DNA Methylation, DNA Transposable Elements, GATA4 Transcription Factor, Kruppel-Like Factor 4, Kruppel-Like Transcription Factors, Leukemia Inhibitory Factor, Male, Mice, Mice, Inbred C57BL, Mouse Embryonic Stem Cells, Pluripotent Stem Cells, Positive Regulatory Domain I-Binding Factor 1, Principal Component Analysis, SOXB1 Transcription Factors, STAT3 Transcription Factor, Transcription Factors

Journal Title

Stem Cell Reports

Conference Name

Journal ISSN

2213-6711
2213-6711

Volume Title

8

Publisher

Cell Press
Sponsorship
Wellcome Trust (096738/Z/11/Z)
Wellcome Trust (092096/Z/10/Z)
Cancer Research Uk (None)
Funding for this study came from a Wellcome Trust program grant (to M.A.S.), and Cancer Research UK (C6946/A14492)/Wellcome Trust (092096) core grants.