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We are interested in transcription factors expressed upon neuronal activity, and their role in memory and plasticity. We use transcriptomics and chromatin profiling methods to address changes in gene expression that arise during the formation and consolidation of long-term olfactory memories.

We investigate how the brain drives changes in food preference under unbalanced diet. We are exploring the neuronal pathways and mechanisms that cause these shifts in dietary choices, aiming to understand key pathways responsible for the state-dependent processing of sensory signals. For this, we use live tracking of food consumption, and single-cell transcriptomics to address changes in gene expression in specific neuronal populations. Our research aims to reveal important insights into feeding behaviour and nutritional health.

Prompted by our recent discovery of dopamine transporter (DAT) expression in a population of non-dopaminergic neurons, we explore how dopamine transport shapes neurotransmission at dopaminergic synapses to influence the balance between learning and forgetting, and signal specificity during memory recall.

We previously identified a series of genes specifically regulated in glial cells upon water deprivation. Our research aims to understand how these genes influence water consumption in thirsty flies, and how they contribute to maintaining brain homeostasis in hyperosmotic conditions.

By enabling gene expression profiling in tens of thousands of individual cells in a single experiment, single-cell transcriptomics has revolutionised life sciences research. We couple these methods to fluorescent cell sorting to address changes in gene expression in very small neuronal populations across the Drosophila brain. We work with Newcastle University’s Genomics Core Facility to perform our RNA-sequencing experiments.

We own state-of-the-art equipment to quantify a large palette of behaviours, include learning and memory, food choice and consumption, sleep and circadian rhythms or locomotion. We are always interested in optimising our assays to quantify behaviour with the highest possible resolution.

We use the microscopy equipment from Durham University’s Bioimaging Facility to reveal details of brain anatomy and track molecules of interest. Recent acquisition of a 2-photon microscope will allow us to perform functional imaging of neuronal activity and dopamine dynamics in live brains.