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Nat. Cell Biol. 17, 1235-1246 (2015)
Transcription factor (TF) networks are thought to regulate embryonic stem cell (ESC) pluripotency. However, TF expression dynamics and regulatory mechanisms are poorly understood. We use reporter mouse ESC lines allowing non-invasive quantification of Nanog or Oct4 protein levels and continuous long-term single-cell tracking and quantification over many generations to reveal diverse TF protein expression dynamics. For cells with low Nanog expression, we identified two distinct colony types: one re-expressed Nanog in a mosaic pattern, and the other did not re-express Nanog over many generations. Although both expressed pluripotency markers, they exhibited differences in their TF protein correlation networks and differentiation propensities. Sister cell analysis revealed that differences in Nanog levels are not necessarily accompanied by differences in the expression of other pluripotency factors. Thus, regulatory interactions of pluripotency TFs are less stringently implemented in individual self-renewing ESCs than assumed at present.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Scopus
Cited By
Cited By
Altmetric
19.679
3.457
77
83
Anmerkungen
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Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Sprache
englisch
Veröffentlichungsjahr
2015
HGF-Berichtsjahr
2015
ISSN (print) / ISBN
1465-7392
e-ISSN
1476-4679
Zeitschrift
Nature Cell Biology
Quellenangaben
Band: 17,
Heft: 10,
Seiten: 1235-1246
Verlag
Nature Publishing Group
Begutachtungsstatus
Peer reviewed
POF Topic(s)
30204 - Cell Programming and Repair
30205 - Bioengineering and Digital Health
30205 - Bioengineering and Digital Health
Forschungsfeld(er)
Stem Cell and Neuroscience
Enabling and Novel Technologies
Enabling and Novel Technologies
PSP-Element(e)
G-500800-001
G-503800-001
G-553800-001
G-503800-001
G-553800-001
PubMed ID
26389663
DOI
10.1038/ncb3237
WOS ID
WOS:000362213500004
Scopus ID
84942981648
Scopus ID
84941905451
Erfassungsdatum
2015-09-30