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@ARTICLE{Cohen:306281,
author = {L. R. Z. Cohen and E. Meshorer},
title = {{T}he many faces of {H}3.3 in regulating chromatin in
embryonic stem cells and beyond.},
journal = {Trends in cell biology},
volume = {34},
number = {12},
issn = {0962-8924},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {DKFZ-2025-02507},
pages = {1044 - 1055},
year = {2024},
note = {#DKFZ-MOST-Ca215#},
abstract = {H3.3 is a highly conserved nonreplicative histone variant.
H3.3 is enriched in promoters and enhancers of active genes,
but it is also found within suppressed heterochromatin,
mostly around telomeres. Accordingly, H3.3 is associated
with seemingly contradicting functions: It is involved in
development, differentiation, reprogramming, and cell fate,
as well as in heterochromatin formation and maintenance, and
the silencing of developmental genes. The emerging view is
that different cellular contexts and histone modifications
can promote opposing functions for H3.3. Here, we aim to
provide an update with a focus on H3.3 functions in early
mammalian development, considering the context of embryonic
stem cell maintenance and differentiation, to finally
conclude with emerging roles in cancer development and cell
fate transition and maintenance.},
subtyp = {Review Article},
keywords = {Histones: metabolism / Humans / Animals / Embryonic Stem
Cells: metabolism / Embryonic Stem Cells: cytology /
Chromatin: metabolism / Cell Differentiation / cancer
(Other) / cell fate (Other) / epigenetics (Other) /
heterochromatin (Other) / pluripotency (Other) /
transcription (Other) / Histones (NLM Chemicals) / Chromatin
(NLM Chemicals)},
ddc = {570},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:38614918},
doi = {10.1016/j.tcb.2024.03.003},
url = {https://inrepo02.dkfz.de/record/306281},
}