Hartmann, Laura ; Kristofori, Panajot ; Li, Congxin ; Becker, Kolja ; Hexemer, Lorenz ; Bohn, Stefan ; Lenhardt, Sonja ; Weiss, Sylvia ; Voss, Björn ; Loewer, Alexander ; Legewie, Stefan (2025)
Transcriptional regulators ensuring specific gene expression and decision-making at high TGFβ doses.
In: Life science alliance, 8 (1)
doi: 10.26508/lsa.202402859
Artikel, Bibliographie
Kurzbeschreibung (Abstract)
TGFβ-signaling regulates cancer progression by controlling cell division, migration, and death. These outcomes are mediated by gene expression changes, but the mechanisms of decision-making toward specific fates remain unclear. Here, we combine SMAD transcription factor imaging, genome-wide RNA sequencing, and morphological assays to quantitatively link signaling, gene expression, and fate decisions in mammary epithelial cells. Fitting genome-wide kinetic models to our time-resolved data, we find that most of the TGFβ target genes can be explained as direct targets of SMAD transcription factors, whereas the remainder show signs of complex regulation, involving delayed regulation and strong amplification at high TGFβ doses. Knockdown experiments followed by global RNA sequencing revealed transcription factors interacting with SMADs in feedforward loops to control delayed and dose-discriminating target genes, thereby reinforcing the specific epithelial-to-mesenchymal transition at high TGFβ doses. We identified early repressors, preventing premature activation, and a late activator, boosting gene expression responses for a sufficiently strong TGFβ stimulus. Taken together, we present a global view of TGFβ-dependent gene regulation and describe specificity mechanisms reinforcing cellular decision-making.
Typ des Eintrags: | Artikel |
---|---|
Erschienen: | 2025 |
Autor(en): | Hartmann, Laura ; Kristofori, Panajot ; Li, Congxin ; Becker, Kolja ; Hexemer, Lorenz ; Bohn, Stefan ; Lenhardt, Sonja ; Weiss, Sylvia ; Voss, Björn ; Loewer, Alexander ; Legewie, Stefan |
Art des Eintrags: | Bibliographie |
Titel: | Transcriptional regulators ensuring specific gene expression and decision-making at high TGFβ doses |
Sprache: | Englisch |
Publikationsjahr: | Januar 2025 |
Verlag: | EMBO Press |
Titel der Zeitschrift, Zeitung oder Schriftenreihe: | Life science alliance |
Jahrgang/Volume einer Zeitschrift: | 8 |
(Heft-)Nummer: | 1 |
DOI: | 10.26508/lsa.202402859 |
Kurzbeschreibung (Abstract): | TGFβ-signaling regulates cancer progression by controlling cell division, migration, and death. These outcomes are mediated by gene expression changes, but the mechanisms of decision-making toward specific fates remain unclear. Here, we combine SMAD transcription factor imaging, genome-wide RNA sequencing, and morphological assays to quantitatively link signaling, gene expression, and fate decisions in mammary epithelial cells. Fitting genome-wide kinetic models to our time-resolved data, we find that most of the TGFβ target genes can be explained as direct targets of SMAD transcription factors, whereas the remainder show signs of complex regulation, involving delayed regulation and strong amplification at high TGFβ doses. Knockdown experiments followed by global RNA sequencing revealed transcription factors interacting with SMADs in feedforward loops to control delayed and dose-discriminating target genes, thereby reinforcing the specific epithelial-to-mesenchymal transition at high TGFβ doses. We identified early repressors, preventing premature activation, and a late activator, boosting gene expression responses for a sufficiently strong TGFβ stimulus. Taken together, we present a global view of TGFβ-dependent gene regulation and describe specificity mechanisms reinforcing cellular decision-making. |
ID-Nummer: | pmid:39542693 |
Zusätzliche Informationen: | Artikel-ID: e202402859 |
Fachbereich(e)/-gebiet(e): | 10 Fachbereich Biologie 10 Fachbereich Biologie > Systems Biology of the Stress Response |
Hinterlegungsdatum: | 18 Nov 2024 13:24 |
Letzte Änderung: | 18 Nov 2024 13:35 |
PPN: | 523625537 |
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