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  Distal and proximal cis-regulatory elements sense X chromosome dosage and developmental state at the Xist locus

Gjaltema, R., Schwämmle, T., Kautz, P., Robson, M., Schöpflin, R., Lustig, L. R., et al. (2022). Distal and proximal cis-regulatory elements sense X chromosome dosage and developmental state at the Xist locus. Molecular Cell, 82(1), 190-208. doi:10.1016/j.molcel.2021.11.023.

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Gjaltema et al_2021.pdf (Verlagsversion), 5MB
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© 2021 The Author(s)

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Gjaltema, Rutger1, Autor           
Schwämmle, Till1, Autor           
Kautz, Pauline1, Autor           
Robson, Michael, Autor
Schöpflin, Robert, Autor
Lustig, Liat Ravid1, Autor           
Brandenburg, Lennart1, Autor
Dunkel, Ilona1, Autor           
Vechiatto, Carolina1, Autor           
Ntini, Evgenia1, Autor
Mutzel, Verena1, Autor           
Schmiedel, Vera1, Autor
Marsico, Annalisa, Autor
Mundlos, Stefan2, Autor           
Schulz, Edda G.1, Autor           
Affiliations:
1Systems Epigenetics (Edda G. Schulz), Independent Junior Research Groups (OWL), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_2117286              
2Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433557              

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Schlagwörter: X-chromosome inactivation Xist CRISPR screens enhancers lncRNA Xert chromatin modifications epigenetics CRISPRi
 Zusammenfassung: Developmental genes such as Xist, which initiates X chromosome inactivation, are controlled by complex cis-regulatory landscapes, which decode multiple signals to establish specific spatiotemporal expression patterns. Xist integrates information on X chromosome dosage and developmental stage to trigger X inactivation in the epiblast specifically in female embryos. Through a pooled CRISPR screen in differentiating mouse embryonic stem cells, we identify functional enhancer elements of Xist at the onset of random X inactivation. Chromatin profiling reveals that X-dosage controls the promoter-proximal region, while differentiation cues activate several distal enhancers. The strongest distal element lies in an enhancer cluster associated with a previously unannotated Xist-enhancing regulatory transcript, which we named Xert. Developmental cues and X-dosage are thus decoded by distinct regulatory regions, which cooperate to ensure female-specific Xist upregulation at the correct developmental time. With this study, we start to disentangle how multiple, functionally distinct regulatory elements interact to generate complex expression patterns in mammals.

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Sprache(n): eng - English
 Datum: 2021-11-232021-12-202022-01-06
 Publikationsstatus: Erschienen
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 Identifikatoren: DOI: 10.1016/j.molcel.2021.11.023
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Titel: Molecular Cell
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge, Mass. : Cell Press
Seiten: - Band / Heft: 82 (1) Artikelnummer: - Start- / Endseite: 190 - 208 Identifikator: ISSN: 1097-2765
CoNE: https://pure.mpg.de/cone/journals/resource/954925610929