Summary: Researchers have identified gene expression signatures common to sensory processing that facilitates the brain’s interpretation of sensory input.
Source: University of Geneva.
Sight, touch and hearing are our windows to the world: these sensory channels send a constant flow of information to the brain, which acts to sort out and integrate these signals, allowing us to perceive the world and interact with our environment. But how do these sensory pathways emerge during development? Do they share a common structure, or, on the contrary, do they emerge independently, each with its specific features? By identifying gene expression signatures common to sight, touch and hearing, neuroscientists at the University of Geneva (UNIGE), Switzerland, discovered a sensory “lingua franca” which facilitates the brain’s interpretation and integration of sensory input. These results, to be read in Nature, pave the way towards a better understanding of perception and communication disorders.
The ability to detect and sort various kinds of stimuli is essential to interact with surrounding objects and people, and to communicate correctly. Indeed, social interaction deficits in people living with autism appear to be partly due difficulties in detecting and interpreting sensory signals. But how does the brain interpret and integrate the stimuli sent by our five senses? It is this very question which Denis Jabaudon, Professor at UNIGE Faculty of Medicine and his team have addressed. ‘We studied the genetic structure of tactile, visual and auditory pathways in mice,’ explains Laura Frangeul, the study first author. ‘By observing neuronal gene expression in these distinct pathways during development, we detected common patterns, as if an underlying genetic language was bringing them together.’
A common language with tailored modulations
The Geneva neuroscientists’ results thus reveal that during development, the various sensory pathways initially share a common gene expression structure, which then adapts to the activity of the organ attached to each sense. ‘This process only takes a few days in mice but could take up to several months in human beings, whose development is much longer and very sensitive to the environment,’ underlines Denis Jabaudon.
This genetic ‘lingua franca’ therefore allows the various sensory pathways to be built according to a similar architecture regardless of their very different functions. It is this shared language that allows the brain to accurately interpret stimuli coming from different sources, and to compose a coherent representation of their combined meaning.
Constant and necessary interactions
Sharing the same building plan also explains how various pathways can mutually balance out, for example when touch or hearing become highly over-developed in people born blind. This discovery also explains why sensory interferences, including synesthesias and hallucinations, can occur in people suffering from neurodevelopmental disorders such as autism or schizophrenia.
Denis Jabaudon concludes: ‘Our results allow us to better understand how the brain circuits which build our representation of the world assemble during development. We are now able to examine how these findings could be put to use to repair them when they fail.’
Source: University of Geneva
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Original Research: Abstract for “A cross-modal genetic framework for the development and plasticity of sensory pathways” by Laura Frangeul, Gabrielle Pouchelon, Ludovic Telley, Sandrine Lefort, Christian Luscher and Denis Jabaudon in Nature. Published online September 26 2016 doi:10.1038/nature19770
A cross-modal genetic framework for the development and plasticity of sensory pathways
Modality-specific sensory inputs from individual sense organs are processed in parallel in distinct areas of the neocortex. For each sensory modality, input follows a cortico–thalamo–cortical loop in which a ‘first-order’ exteroceptive thalamic nucleus sends peripheral input to the primary sensory cortex, which projects back to a ‘higher order’ thalamic nucleus that targets a secondary sensory cortex. This conserved circuit motif raises the possibility that shared genetic programs exist across sensory modalities. Here we report that, despite their association with distinct sensory modalities, first-order nuclei in mice are genetically homologous across somatosensory, visual, and auditory pathways, as are higher order nuclei. We further reveal peripheral input-dependent control over the transcriptional identity and connectivity of first-order nuclei by showing that input ablation leads to induction of higher-order-type transcriptional programs and rewiring of higher-order-directed descending cortical input to deprived first-order nuclei. These findings uncover an input-dependent genetic logic for the design and plasticity of sensory pathways, in which conserved developmental programs lead to conserved circuit motifs across sensory modalities.
“A cross-modal genetic framework for the development and plasticity of sensory pathways” by Laura Frangeul, Gabrielle Pouchelon, Ludovic Telley, Sandrine Lefort, Christian Luscher and Denis Jabaudon in Nature. Published online September 26 2016 doi:10.1038/nature19770