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  Histone variant H2A.Z regulates zygotic genome activation

Ibarra-Morales, D., Rauer, M., Quarato, P., Rabbani, L., Zenk, F., Schulte-Sasse, M., et al. (2021). Histone variant H2A.Z regulates zygotic genome activation. Nature Communications, 12: 7002. doi:10.1038/s41467-021-27125-7.

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Ibarra-Morales et al. 2021.pdf (Verlagsversion), 4MB
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https://www.nature.com/articles/s41467-021-27125-7 (Verlagsversion)
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 Urheber:
Ibarra-Morales, Dafne1, Autor
Rauer, Michael2, Autor
Quarato, Piergiuseppe3, Autor
Rabbani, Leily2, Autor
Zenk, Fides1, Autor
Schulte-Sasse, Mariana1, Autor
Cardamone, Francesco1, Autor
Gomez-Auli, Alejandro2, Autor
Cecere, Germano3, Autor
Iovino, Nicola1, Autor           
Affiliations:
1Department of Chromatin Regulation, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243643              
2Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_persistent22              
3External Organizations, ou_persistent22              

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 Zusammenfassung: During embryogenesis, the genome shifts from transcriptionally quiescent to extensively active in a process known as Zygotic Genome Activation (ZGA). In Drosophila, the pioneer factor Zelda is known to be essential for the progression of development; still, it regulates the activation of only a small subset of genes at ZGA. However, thousands of genes do not require Zelda, suggesting that other mechanisms exist. By conducting GRO-seq, HiC and ChIP-seq in Drosophila embryos, we demonstrate that up to 65% of zygotically activated genes are enriched for the histone variant H2A.Z. H2A.Z enrichment precedes ZGA and RNA Polymerase II loading onto chromatin. In vivo knockdown of maternally contributed Domino, a histone chaperone and ATPase, reduces H2A.Z deposition at transcription start sites, causes global downregulation of housekeeping genes at ZGA, and compromises the establishment of the 3D chromatin structure. We infer that H2A.Z is essential for the de novo establishment of transcriptional programs during ZGA via chromatin reorganization.

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Sprache(n): eng - English
 Datum: 2021-12-01
 Publikationsstatus: Online veröffentlicht
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 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1038/s41467-021-27125-7
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Titel: Nature Communications
  Kurztitel : Nat. Commun.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: London : Nature Publishing Group
Seiten: - Band / Heft: 12 Artikelnummer: 7002 Start- / Endseite: - Identifikator: ISSN: 2041-1723
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723