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Haubensak, W.

Publications and source records attributed to Haubensak, W..

4 recordsLinked to original sources

BrainTACO: An Explorable Multi-Scale Multi-Modal Brain Transcriptomic And Connectivity Data Resource

AbstractExploring the relationships between genes, brain circuitry, and behaviour is accelerated by the joint analysis of a heterogeneous sets form 3D imaging data, anatomical data, and brain networks at varying scales, res-olutions, and modalities. Hence, generating an integrated view, beyond the individual resources original purpose, requires the fusion of these data to a common space, and a visualization that bridges the gap across scales. However, despite ever expanding datasets, few plat-forms for integration and exploration of this heterogeneous data exist. To this end, we present the BrainTACO (Brain Transcriptomic And Connectivity Data) resource, a selection of heterogeneous, and multi-scale neurobiological data spatially mapped onto a common, hierarchical reference space, combined via a holistic data integration scheme. To access BrainTACO, we extended BrainTrawler, a web-based visual ana-lytics framework for spatial neurobiological data, with comparative visualizations of multiple resources for gene expression dissection of brain networks with an unprecedented coverage. Using this platform, allows to straightforward explore and extract brain data for identifying potential genetic drivers of connectivity in both mice and humans that may contribute to the discovery of dysconnectivity phenotypes. Hence, BrainTACO reduces the need for time-consuming manual data aggregation often required for computational analyses in script based toolboxes, and supports neuroscientists by focusing on leveraging the data instead of preparing it.

bioinformatics↗

Rapid nucleus-scale reorganization of chromatin in neurons enables transcriptional adaptation for memory consolidation

The interphase nucleus is functionally organized in active and repressed territories defining the transcriptional status of the cell. However, it remains poorly understood how the nuclear architecture of neurons adapts in response to behaviorally relevant stimuli that trigger fast alterations in gene expression patterns. Imaging of fluorescently tagged nucleosomes revealed that pharmacological manipulation of neuronal activity in vitro and auditory cued fear conditioning in vivo induce nucleus-scale restructuring of chromatin within minutes. Furthermore, the acquisition of auditory fear memory is impaired after infusion of a drug into auditory cortex which blocks chromatin reorganization in vitro. We propose that active chromatin movements at the nucleus scale act together with local gene-specific modifications to enable transcriptional adaptations at fast time scales. Introducing a transgenic mouse line for photolabeling of histones, we extend the realm of systems available for imaging of chromatin dynamics to living animals.

neuroscience↗

Molecular archaeology of the human brain

Mapping the origin of human cognitive traits typically relies on comparing behavioral or neuroanatomical features in human phylogeny. However, such studies rely on inferences from comparative relationships and do not incorporate neurogenetic information, as these approaches are restricted to experimentally accessible species. Here, we fused evolutionary genomics with human functional neuroanatomy to reconstruct the neurogenetic evolution of human brain functions more directly and comprehensively. Projecting genome-wide selection pressure (dN/dS ratios) in sets of chronologically ordered mammalian species onto the human brain reference space unmasked spatial patterns of cumulative neurogenetic selection and co-evolving brain networks from task-evoked functional MRI and functional neuroanatomy. Importantly, this evolutionary atlas allowed imputing functional features to archaic brains from extinct hominin genomes. These data suggest accelerated neurogenetic selection for language and verbal communication across all hominin lineages. In addition, the predictions identified strategic thought and decision making as the dominant traits that may have separated anatomically modern humans (AMH) from archaic hominins.

bioinformatics↗

A Data Structure for real-time Aggregation Queries of Big Brain Networks

Recent advances in neuro-imaging allowed big brain-initiatives and consortia to create vast resources of brain data that can be mined by researchers for their individual projects. Exploring the relationship between genes, brain circuitry, and behavior is one of key elements of neuroscience research. This requires fusion of spatial connectivity data at varying scales, such as whole brain correlated gene expression, structural and functional connectivity. With ever-increasing resolution, those exceed the past state-of-the art in several orders of magnitude in size and complexity. Current analytical workflows in neuroscience involve time-consuming manual aggregation of the data and only sparsely incorporate spatial context to operate continuously on multiple scales. Incorporating techniques for handling big connectivity data is therefore a necessity.\n\nWe propose a data structure to explore heterogeneous neurobiological connectivity data for integrated visual analytics workflows. Aggregation Queries, i.e. the aggregated connectivity from, to or between brain areas allow experts the comparison of multimodal networks residing at different scales, or levels of hierarchically organized anatomical atlases. Executed on-demand on volumetric gene expression and connectivity data, they enable an interactive dissection of networks, with billions of edges, in real-time, and based on their spatial context. The data structure is optimized to be accessed directly from the hard disk, since connectivity of large-scale networks typically exceed the memory size of current consumer level PCs. This allows experts to embed and explore their own experimental data in the framework of public data resources without large-scale infrastructure.\n\nOur novel data structure outperforms state-of-the-art graph engines in retrieving connectivity of local brain areas experimentally. We demonstrate the application of our approach for neuroscience by analyzing fear-related functional neuroanatomy in mice. Further, we show its versatility by comparing multimodal brain networks linked to autism. Importantly, we achieve cross-species congruence in retrieving human psychiatric traits networks, which facilitates selection of neural substrates to be further studied in mouse models.

neuroscience↗