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Mannervik Lab

@mannerviklab.bsky.social
112 followers 167 following 12 posts

We study developmental epigenetics using fruit flies www.su.se/english/research/research…

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Mannervik Lab @mannerviklab.bsky.social · 02/06/2026
Led by Sergei Pirogov @biologsp.bsky.social , with key contributions from Artem Ilin @adc34.bsky.social , Aleksander Purik, and collaborators.
The model of
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Mannervik Lab @mannerviklab.bsky.social · 02/06/2026
We tested this idea by partially depleting H3K27me3 in the mesoderm, which led to reactivation of genes normally expressed in closely related cell populations.
Epigenetic landscapes for the Krüppel gene locus in wild-type embryos and embryos with a mesoderm-specific knockdown of Polycomb catalytic subunit E(z), which deposits H3K27me3. After knockdown, the repressive "hill" diminishes along the muscle (M) trajectory, and Krüppel is ectopically expressed in muscles.
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Mannervik Lab @mannerviklab.bsky.social · 02/06/2026
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.
On the top, epidermal (hindgut) TF byn is expressed and accessible exclusively in the epidermal lineage, and Polycomb-repressed only in the same lineage. However, TF so, expressed at this stage only in muscles, is accessible in all cell types, and repressed everywhere, except muscles. We conclude that Polycomb-mediated repression silences genes with accessible promoters, which probably receive activation cues. When nucleosomes occlude a gene promoter, Polycomb repression is often not necessary.
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Mannervik Lab @mannerviklab.bsky.social · 02/06/2026
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.
We can add the third dimension, which subtracts the active (H3K27ac) signal from the repressive (H3K27me3) signal for a particular gene locus (e.g., epidermal TF vvl). It creates "valleys" permissive for transcription, surrounded by the repressive "hills". The permissiveness increased in the epidermal trajectory, as well as the repressive mark accumulated in endomesodermal trajectories during development. On the right, we project the vvl expression level inferred from the scRNA-seq dataset. Therefore, our visualization can show levels of expression, H3K27-acetylation and -methylation across cell types and along the developmental time
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Mannervik Lab @mannerviklab.bsky.social · 02/06/2026
We applied nanoCUT&Tag to developing Drosophila embryos at different stages and looked into the distribution of marks across cell types.
On the left, the UMAP visualization of nanoCUT&Tag Drosophila nuclei from 8 to 16 hours of development. On the right, cell-time embedding, where cells are placed according to their developmental cell age (y-axis) and cell lineage (x-axis). We have distinguished five main fly embryo cell types: epidermis, fat body, muscle, midgut and neuronal
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