Mattias Mannervik

The paper identifies and characterizes two related Transib elements in Drosophila, showing contrasting invasion patterns and genomic impacts.

The paper uses dual-modality nano-CUT&Tag to analyze H3K27ac and H3K27me3 in Drosophila embryos, revealing lineage-specific Polycomb repression and epigenetic potential landscapes.

The paper identifies ERK signaling as a suppressor of chaperone-mediated autophagy (CMA) and shows that inhibiting ERK can restore CMA by increasing LAMP-2A expression.

This study shows that CBP, a histone acetyltransferase, has both catalytic and non-catalytic roles in zygotic genome activation, independent of its acetylation function.

The paper investigates how chromatin state influences transcriptional burst kinetics and RNA Polymerase II pausing during Drosophila embryonic patterning.

This study demonstrates that HDAC3's repressor and activator functions can be genetically separated in Drosophila, revealing distinct roles for catalytic activity and SMRTER interaction in transcriptional regulation.

This study shows that the transcription factor GAF acts as a stable mitotic bookmark during zygotic genome activation in Drosophila embryos, enabling rapid transcriptional activation after mitosis.

The paper shows that 3D chromatin organisation and gene regulation are independent during Drosophila dorsoventral patterning, with chromatin structure maintaining consistency across tissues despite differences in gene expression.