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Twitter account for Mattias Mannervik lab at Stockholm University. Transcription and epigenetics in Drosophila.

Joined February 2021
Photo by Mannervik Lab (@MannervikLab)Photo by Mannervik Lab (@MannervikLab)Photo by Mannervik Lab (@MannervikLab)Photo by Mannervik Lab (@MannervikLab)Photo by Mannervik Lab (@MannervikLab)Photo by Mannervik Lab (@MannervikLab)Photo by Mannervik Lab (@MannervikLab)Photo by Mannervik Lab (@MannervikLab)Photo by Mannervik Lab (@MannervikLab)Photo by Mannervik Lab (@MannervikLab)
Led by Sergei Pirogov @biologsp, with key contributions from Artem Ilin, Aleksander Purik, and collaborators.
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We tested this idea by partially depleting H3K27me3 in the mesoderm, which led to reactivation of genes normally expressed in closely related cell populations.
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In other lineages, these same genes were often silent without H3K27me3 and instead had low promoter accessibility. This suggests that Polycomb repression is especially important when a gene promoter is accessible and exposed to activating inputs.
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Our interpretation is that these genes are active only in specific cell subtypes within that lineage. Polycomb repression likely acts in the other cells of the same lineage, preventing inappropriate activation.
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Many genes were repressed by H3K27me3 only in one cell lineage, and this was often the same lineage in which the gene is normally expressed. How can a gene be both expressed and Polycomb-repressed in the same lineage?
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Second, lineage-determining transcription factors are repressed in lineages where they are not expressed (as in the case of vvl). But the third pattern was the most unexpected.
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We also revealed that Polycomb does not repress genes in the same way across cell types. First, classical Polycomb targets such as Hox genes are repressed broadly across cell types.
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We introduce a new way to visualize multidimensional single-cell epigenetic data, including an “epigenetic potential” landscape that combines developmental time, cell type, and antagonistic chromatin marks in a single framework.
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nanoCUT&Tag profiles active H3K27ac and repressive H3K27me3 simultaneously in the same nucleus. We applied it to developing Drosophila embryos at different stages and looked into the distribution of marks across cell types.
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Have you ever wondered how chromatin states shape developmental trajectories? In our preprint, we address this question using single-cell nanoCUT&Tag, a method developed by Marek Bartosovic @marekbartosovic, biorxiv.org/content/10.64898…
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Curious about epigenetics, gene regulation, and developmental biology? Apply for the PhD position in Mannervik lab at Stockholm University! We use single-cell genomics and genetic approaches to uncover how cells acquire their identities during development.
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Mannervik Lab retweeted
Using PRO-seq and CUT&Tag, we found that CBP activates zygotic genes in two steps: - It helps recruit RNA Pol II to promoters without requiring catalytic activity. - Its catalytic acetyltransferase function then triggers pause release.
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Mannervik Lab retweeted
Excited to share our new paper in @MolecularCell Mol Cell: "Catalytic-dependent and independent functions of the histone acetyltransferase CBP promote pioneer-factor-mediated zygotic genome activation" — the big part of my PhD! cell.com/molecular-cell/full…
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Horizon Europe research-and-innovation.ec.e… SCENTINEL members are grateful to HE for supporting Drosophila Research and the transfer of expertise in single cell omics across Europe
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Welcome to SCENTINEL! a Horizon Europe Twinning collaborative initiative between @IMBB_FORTH (Delidakis lab, Lavigne lab, Genomics CF) @IRBBarcelona (Bioinformatics and Functional Genomics CF) @IJMonod (Konstantinides lab) @IGBMC (Giangrande lab) @Stockholm_Uni (Mannervik lab)
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Mannervik Lab retweeted
📢 One of the @FEBS_Letters #PosterPrize awarded at the Transcription & Chromatin #EMBLTranscript conference in Heidelberg goes to🥁.... Sergei Pirogov! Congratulations, Sergei! 👏👏👏 @MannervikLab @Stockholm_Uni @EMBLEvents
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✳️✳️✳️✳️✳️✳️Please RT !! ✳️✳️✳️✳️✳️✳️ Register NOW For our #DevBio Meeting ❤️🪰🐁🪱🐸 In May 28-31, 2024 in spectacular Bergen (Norway 🇳🇴☀️⛰️⛵️) Look at our marvellous speakers line-up ⬇️ tinyurl.com/NDEVMSS24
📢 Registration is open!! We are thrilled to announce registration for the 'Nordic Developmental Biology Societies & Michael Sars Symposium Joint Meeting' on May 28-31, 2024 is open! Organized in collaboration with @swedbo & FSDB @UiB ✨REGISTER HERE ➡️ tinyurl.com/NDEVMSS24
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A big thanks to Rickard Sandberg and Christoph Ziegenhain @chris_zie for the nice collaboration on bursting and to Johan Reimegård @johan_rei for all bioinformatic help. It’s been a true pleasure to collaborate on this exciting project!
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