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@ARTICLE{Jaber:180371,
author = {M. Jaber and A. Radwan and N. Loyfer and M. Abdeen and S.
Sebban and A. Khatib and H. Yassen and T. Kolb$^*$ and M.
Zapatka$^*$ and K. Makedonski and A. Ernst$^*$ and T. Kaplan
and Y. Buganim},
title = {{C}omparative parallel multi-omics analysis during the
induction of pluripotent and trophectoderm states.},
journal = {Nature Communications},
volume = {13},
number = {1},
issn = {2041-1723},
address = {[London]},
publisher = {Nature Publishing Group UK},
reportid = {DKFZ-2022-01285},
pages = {3475},
year = {2022},
abstract = {Following fertilization, it is only at the 32-64-cell stage
when a clear segregation between cells of the inner cell
mass and trophectoderm is observed, suggesting a 'T'-shaped
model of specification. Here, we examine whether the
acquisition of these two states in vitro, by nuclear
reprogramming, share similar dynamics/trajectories. Using a
comparative parallel multi-omics analysis (i.e., bulk
RNA-seq, scRNA-seq, ATAC-seq, ChIP-seq, RRBS and CNVs) on
cells undergoing reprogramming to pluripotency and TSC state
we show that each reprogramming system exhibits specific
trajectories from the onset of the process, suggesting
'V'-shaped model. We describe in detail the various
trajectories toward the two states and illuminate
reprogramming stage-specific markers, blockers, facilitators
and TSC subpopulations. Finally, we show that while the
acquisition of the TSC state involves the silencing of
embryonic programs by DNA methylation, during the
acquisition of pluripotency these regions are initially
defined but retain inactive by the elimination of H3K27ac.},
cin = {B420 / HD01 / B060},
ddc = {500},
cid = {I:(DE-He78)B420-20160331 / I:(DE-He78)HD01-20160331 /
I:(DE-He78)B060-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:35715410},
doi = {10.1038/s41467-022-31131-8},
url = {https://inrepo02.dkfz.de/record/180371},
}