I study how an embryo switches on its first genes. In the hours after fertilisation, control passes from the mother’s mRNAs and proteins to the embryo’s own genome: pioneer factors open chromatin, histone marks inherited from the egg or written from metabolites decide which genes respond first, and mRNA–protein condensates keep maternal messages silent and in place until they are needed.
My work connects three active questions in the field: how metabolic state reaches chromatin at genome activation, how the material state of RNA–protein granules controls when their mRNAs are read, and how the same metabolic signals shape the behaviour of the whole animal. I bring fruit-fly genetics, single-molecule imaging and quantitative image analysis.
Master’s research, Max Planck Institute of Immunobiology and Epigenetics, Freiburg (2026–27): metabolism and histone modifications at the maternal-to-zygotic transition, and metabolism and behaviour.
Gene expression across regulatory layers
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Text description and references
One cell, four chapters. Chromatin state: a pioneer factor opens an enhancer; acetyl, lactyl and methyl marks appear, fed by acetyl-CoA, lactyl-CoA and SAM from mitochondria and gut microbes; a cohesin loop brings enhancer and promoter together. Transcriptional bursting: Pol II fires in bursts and mRNAs are exported. mRNA fate: RBPs bind; some mRNAs are deadenylated and decayed, others are held in an RNP granule that grows by fusion and later released for translation. Protein, metabolism and feedback: enzymes drive metabolic flux, metabolites and regulators return to chromatin, and metabolic state links to behaviour. Inset: maternal mRNA, zygotic mRNA and protein over developmental time (schematic).
I am also building this site into a platform where biology research feels easy and explorative: visual explanations of methods and ideas, and free, open tools for biologists that run in the browser, with no sign-up. Images and files you analyse stay on your own computer.