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Regulation of mammalian totipotency: A molecular perspective from in vivo and in vitro studies.
Curr. Opin. Genet. Dev. 81:102083 (2023)
In mammals, cells acquire totipotency at fertilization. Embryonic genome activation (EGA), which occurs at the 2-cell stage in the mouse and 4- to 8-cell stage in humans, occurs during the time window at which embryonic cells are totipotent and thus it is thought that EGA is mechanistically linked to the foundations of totipotency. The molecular mechanisms that lead to the establishment of totipotency and EGA had been elusive for a long time, however, recent advances have been achieved with the establishment of new cell lines with greater developmental potential and the application of novel low-input high-throughput techniques in embryos. These have unveiled several principles of totipotency related to its epigenetic makeup but also to characteristic features of totipotent cells. In this review, we summarize and discuss current views exploring some of the key drivers of totipotency from both in vitro cell culture models and embryogenesis in vivo.
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Anmerkungen
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Review
Schlagwörter
Chromatin Assembly Factor-1; Zygotic Genome Activation; Embryonic-like Cells; Gene-expression; Stem-cells; Mouse; Dux; Transcription; Populations; Metabolism
Sprache
englisch
Veröffentlichungsjahr
2023
HGF-Berichtsjahr
2023
ISSN (print) / ISBN
0959-437X
e-ISSN
1879-0380
Zeitschrift
Current Opinion in Genetics & Development
Quellenangaben
Band: 81,
Artikelnummer: 102083
Verlag
Elsevier
Verlagsort
84 Theobalds Rd, London Wc1x 8rr, England
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Epigenetics and Stem Cells (IES)
POF Topic(s)
30204 - Cell Programming and Repair
Forschungsfeld(er)
Stem Cell and Neuroscience
PSP-Element(e)
G-506200-001
Förderungen
German Research Foundation (DFG) through the CRC Chromatin Dynamics
National Institutes of Health (NIH)
Helmholtz Association
National Institutes of Health (NIH)
Helmholtz Association
WOS ID
001040869700001
Scopus ID
85164212924
PubMed ID
37421903
Erfassungsdatum
2023-10-06