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Kohler, S.

Publications and source records attributed to Kohler, S..

2 recordsLinked to original sources

Animacy and real world size shape object representations in the human medial temporal lobes

Identifying what an object is, and whether an object has been encountered before, is a crucial aspect of human behavior. Despite this importance, we do not have a complete understanding of the neural basis of these abilities. Investigations into the neural organization of human object representations have revealed category specific organization in the ventral visual stream in perceptual tasks. Interestingly, these categories fall within broader domains of organization, with distinctions between animate, inanimate large, and inanimate small objects. While there is some evidence for category specific effects in the medial temporal lobe (MTL), it is currently unclear whether domain level organization is also present across these structures. To this end, we used fMRI with a continuous recognition memory task. Stimuli were images of objects from several different categories, which were either animate or inanimate, or large or small within the inanimate domain. We employed representational similarity analysis (RSA) to test the hypothesis that object-evoked responses in MTL structures during recognition-memory judgments also show evidence for domain-level organization along both dimensions. Our data support this hypothesis. Specifically, object representations were shaped by either animacy, real-world size, or both, in perirhinal and parahippocampal cortex, as well as the hippocampus. While sensitivity to these dimensions differed when structures when probed individually, hinting at interesting links to functional differentiation, similarities in organization across MTL structures were more prominent overall. These results argue for continuity in the organization of object representations in the ventral visual stream and the MTL.

neuroscience

Super-resolution microscopy reveals the three-dimensional organization of meiotic chromosome axes in intact C. elegans tissue

When cells enter meiosis, their chromosomes reorganize as linear arrays of chromatin loops anchored to a central axis. Meiotic chromosome axes form a platform for the assembly of the synaptonemal complex (SC), and play central roles in other meiotic processes, including homologous pairing, recombination, and chromosome segregation. However, little is known about the three-dimensional organization of components within the axes, which consist of cohesin complexes and additional meiosis-specific proteins. Here we investigate the molecular organization of meiotic chromosome axes in C. elegans through STORM and PALM superresolution imaging of intact germline tissue. By tagging one axis protein (HIM-3) with a photoconvertible fluorescent protein, we established a spatial reference for other components, which were localized using antibodies against epitope tags inserted by CRISPR/Cas9 genome editing. Using three-dimensional averaging, we determined the 3D-organization of all known components within synapsed chromosome axes to a precision of 2-5 nanometers. We find that meiosis-specific HORMA-domain proteins span a gap between cohesin complexes and the central region of the SC, consistent with their essential roles in SC assembly. Our data further suggest that the two different meiotic cohesin complexes are distinctly arranged within the axes: Cohesin complexes containing COH-3 or -4 kleisins form a central core in the central plane of the axes, whereas complexes containing REC-8 kleisin protrude above and below the plane defined by the SC. This splayed organization may help to explain the role of the chromosome axes in promoting inter-homolog repair of meiotic double strand breaks by inhibiting inter-sister repair.

cell biology