Active Brain & Nervous System Psychology & Behaviour

Understanding brain asymmetry: from genes and developmental mechanisms to circuits and behaviour

In plain English

AI plain-English summary

The left and right sides of a zebrafish brain develop differently, and researchers are systematically mapping how that asymmetry arises, how it wires into neural circuits, and what it does to behaviour. This matters because left–right differences are universal across animal nervous systems, yet scientists know almost nothing about how they form, how they are encoded in brain circuits, or what functional roles they play. The team will study the habenula—a brain region that connects emotion and decision-making—in zebrafish, a transparent species that allows direct observation of neural activity. They will use a large-scale CRISPR/Cas9 screen to find new genes controlling asymmetry, focus on a protein called Cachd1 that modulates asymmetric neuron growth, and combine calcium imaging with spatial transcriptomics to compare left- and right-sided neurons at the level of both gene expression and electrical activity. This is fundamental science. There is no immediate clinical or engineering application. But understanding how a brain builds and uses structural asymmetry could eventually illuminate conditions such as schizophrenia or autism, where normal lateralisation is disrupted. Past discoveries in brain asymmetry have already informed treatments for stroke recovery and language disorders.

View original technical description
Despite left-right asymmetry being a universal feature of animal nervous systems, we understand little about how such asymmetries arise, how they are encoded in circuits and what roles they play in nervous system function. Our programme of research will elucidate all these aspects of brain asymmetry through the implementation of a comprehensive genetic, developmental, physiological and behavioural platform to study habenular lateralisation in zebrafish. Our first aim is to resolve the developmental processes that establish habenular asymmetry. One focus will be on Cachd1, a transmembrane Wnt-receptor binding protein that modulates asymmetric neurogenesis; additionally, we will perform a large-scale Crispr/Cas9-based screen to identify novel genes that influence habenular asymmetry. Next, we aim to understand how lateralised neurons diversify and will combine functional calcium imaging with spatial transcriptomics to explore the emergence of neuronal diversity in terms of transcriptional and physiological profiles of left- and right-sided habenular neurons. To understand the functional consequences of normal and disrupted brain asymmetry, we will characterise a range of innate behaviours, including context-dependent exploration, in wild-type and mutant animals. Finally, by subjecting our multimodal datasets to methods including canonical correlation analysis and directly manipulating circuit activity, we will determine how neural asymmetry impacts behavioural outcomes.

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Researchers

Isaac Bianco (EPMC Awardee)Stephen Wilson (EPMC Awardee)

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Original classification

Discovery Award

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