Completed Cells, Biochemistry & Physiology Genetics & Molecular Biology

The asymmetric brain: from genes to circuits and behaviour.

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The left and right halves of a zebrafish brain do not develop identically, and researchers are watching that asymmetry emerge cell by cell to understand how it happens in all vertebrates. This matters because brain asymmetry—where structures on the left and right differ in size, shape, or wiring—is essential for efficient cognition, yet the mechanisms that create it remain poorly understood. When asymmetry goes wrong, it is linked to conditions such as schizophrenia and autism spectrum disorders. The team uses larval zebrafish, whose transparent bodies allow direct observation of developing neurons, to tackle four questions: how symmetry is first broken, how different asymmetries align with each other, what circuits the asymmetric neurons join, and how those circuits drive behaviour. This is fundamental science with no immediate clinical application. But understanding how the brain builds its left–right differences at the genetic and cellular level could eventually reveal why those processes fail in neurodevelopmental disorders. Past work on asymmetry in fish has already uncovered signalling pathways—such as Nodal and Fgf—that operate in human brains too, making this a plausible route toward identifying targets for future therapies.

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Asymmetry is a fundamental, yet poorly understood, feature of the CNS, critical for efficient cognitive function and disrupted in various neuropathologies. We have established the larval zebrafish as a powerful model for studying many aspects of CNS asymmetry. Our goals for this programme of research are to resolve the mechanisms by which symmetry is broken, to determine how concordance between neuroanatomical asymmetries is achieved, to elucidate the circuitry into which asymmetric neurons a re incorporated and to link activity in asymmetric circuits to behaviour. Fgf signalling is required for the leftward migration of the parapineal and we will determine how activation of this pathway is localised to leading cells of the migrating primordium. We will also address whether and how, this activation is dependent upon localised Nodal signalling. Subsequent to migration, the parapineal imposes asymmetry upon the left habenula and we will clone novel mutations in which this comm unication is disrupted and will resolve the role of Wnt signalling in this process. We will use powerful transgenesis techniques to resolve the circuitry of the epithalamic nuclei and will refine assays for behaviours that are influenced by neuroanatomical lateralisation. Finally we will directly link circuit activity to behaviour in free-swimming fry.

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Researchers

Stephen Wilson (EPMC Awardee)

Related Research

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Programme Grant

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