Unknown

Dataset Information

0

Genome-wide dynamics of replication timing revealed by in vitro models of mouse embryogenesis.


ABSTRACT: Differentiation of mouse embryonic stem cells (mESCs) is accompanied by changes in replication timing. To explore the relationship between replication timing and cell fate transitions, we constructed genome-wide replication-timing profiles of 22 independent mouse cell lines representing 10 stages of early mouse development, and transcription profiles for seven of these stages. Replication profiles were cell-type specific, with 45% of the genome exhibiting significant changes at some point during development that were generally coordinated with changes in transcription. Comparison of early and late epiblast cell culture models revealed a set of early-to-late replication switches completed at a stage equivalent to the post-implantation epiblast, prior to germ layer specification and down-regulation of key pluripotency transcription factors [POU5F1 (also known as OCT4)/NANOG/SOX2] and coinciding with the emergence of compact chromatin near the nuclear periphery. These changes were maintained in all subsequent lineages (lineage-independent) and involved a group of irreversibly down-regulated genes, at least some of which were repositioned closer to the nuclear periphery. Importantly, many genomic regions of partially reprogrammed induced pluripotent stem cells (piPSCs) failed to re-establish ESC-specific replication-timing and transcription programs. These regions were enriched for lineage-independent early-to-late changes, which in female cells included the inactive X chromosome. Together, these results constitute a comprehensive "fate map" of replication-timing changes during early mouse development. Moreover, they support a model in which a distinct set of replication domains undergoes a form of "autosomal Lyonization" in the epiblast that is difficult to reprogram and coincides with an epigenetic commitment to differentiation prior to germ layer specification.

SUBMITTER: Hiratani I 

PROVIDER: S-EPMC2813472 | biostudies-literature | 2010 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Genome-wide dynamics of replication timing revealed by in vitro models of mouse embryogenesis.

Hiratani Ichiro I   Ryba Tyrone T   Itoh Mari M   Rathjen Joy J   Kulik Michael M   Papp Bernadett B   Fussner Eden E   Bazett-Jones David P DP   Plath Kathrin K   Dalton Stephen S   Rathjen Peter D PD   Gilbert David M DM  

Genome research 20091201 2


Differentiation of mouse embryonic stem cells (mESCs) is accompanied by changes in replication timing. To explore the relationship between replication timing and cell fate transitions, we constructed genome-wide replication-timing profiles of 22 independent mouse cell lines representing 10 stages of early mouse development, and transcription profiles for seven of these stages. Replication profiles were cell-type specific, with 45% of the genome exhibiting significant changes at some point during  ...[more]

Similar Datasets

2010-05-19 | E-GEOD-18019 | biostudies-arrayexpress
2009-11-25 | GSE18019 | GEO
2010-05-19 | E-GEOD-17980 | biostudies-arrayexpress
2009-11-25 | GSE17980 | GEO
| PRJNA119253 | ENA
| S-EPMC2950085 | biostudies-other
2023-10-16 | GSE218365 | GEO
2018-10-20 | GSE121537 | GEO
2007-08-14 | E-GEOD-6977 | biostudies-arrayexpress
| S-EPMC2967475 | biostudies-literature