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Heinrich, R.

Publications and source records attributed to Heinrich, R..

2 recordsLinked to original sources

A novel approach to quantifying inter-individual distance in insects

1Behaviour involving two or more individuals within the same species is known as social behaviour. Sexual dimorphisms and environmental cues as well as age, experience and social hierarchy shape social behaviour. The study of this complex behaviour, however, has one essential boundary condition: the distance between individuals. Because social signals (e.g. acoustic, visual or olfactory) have limited reach the inter-individual distance is crucial for the correct transmission of such signals. In this study we present a newly developed assay to study group behaviour and inter-individual distance in Drosophila melanogaster. This assay consists of a circular observation space flanked by two automatic release devices that allow flies to enter individually. By releasing the flies one at a time, the observer can study different features of (intra-)group behaviour with different group compositions. Importantly, the observer can control (manually or through automatisation) the increase of group size over time. Over the last decades insects became more relevant as convenient model organisms to study the neurophysiological and genetic basis of (human) neuro-developmental disorders. Drosophila models are used to study the genetic and neuronal underpinnings of a wide range of neurological disorders. In some cases the studies revealed alterations in social behaviour consistent with descriptions of behavioural symptoms in human disorders. Social behaviours in Drosophila are well-studied and include courtship, mating, aggression and group interactions. This setup will facilitate the analysis of these aspects of group interactions in Drosophila, allowing for a deeper understanding of the neuronal circuits and genetic factors involved in those behaviours. 2 Contribution to the fieldSocial behaviour pertains to the most sophisticated behavioural feats, as it involves multiple, interacting individuals. These complex interactions often conceal the underlying neuronal and ethological mechanisms. One of the most basal ethological mechanisms is the inter-individual distance, which resembles a perimeter in which each individual needs to formulate a response to the approach of others. We introduce a device that allows to test the inter-individual distance under consistent circumstances, by automating the entry time and direction of conspecifics into the arena. We can further observe the composition, dynamics and forming of larger animal groups as well as their separating. We can also observe how the individual distances alter during the process. Also other behaviours can be easily observed, e.g. aggression, courtship, homosexual courtship, etc. We successfully employed this approach in [1] and could discriminate the role of different neuroligins in social behaviour. We provide a detailed description including building plans and material lists for this social observation device. The system can be run in an automatic mode to ensure the consistency of experiments or in a manual mode to test animals under more flexible social situations. We provide multiple back lighting systems to test animals in the dark (infra-red LEDs) or in illuminated environments (vis. range LEDs). The system is fully automated and can be linked with a number of animal trackers (e.g. T-Rex, deeplabcut, LACE, etc.) via simple videography. We hope that our experimental setup augments the variety of behaviours testable in ethological setups (T-maze, water-mazes, operant conditing setups, etc) with social interaction and group formation.

animal behavior and cognition↗

Differential roles for DNAJ isoforms in HTT-polyQ and mutant FUS aggregation modulation revealed by chaperone network screens

Protein aggregation is a hallmark of many neurodegenerative diseases1,2. In order to cope with misfolding and aggregation, cells have evolved an elaborate network of molecular chaperones, composed of different families3. But while chaperoning mechanisms for different families are well established, functional and regulatory diversification within chaperone families is still largely a mystery4,5. Here we decided to explore chaperone functional diversity, through the lens of pathological aggregation. We revealed that different naturally-occurring isoforms of DNAJ chaperones showed differential effects on different types of aggregates. We performed a chaperone screen for modulators of two neurodegeneration-related aggregating proteins, the Huntingtons disease-related HTT-polyQ, and the ALS-related mutant FUS (mutFUS). The screen identified known modulators of HTT-polyQ aggregation6,7, confirming the validity of our approach. Surprisingly, modulators of mutFUS aggregation were completely different than those of HTT-polyQ. Interestingly, different naturally-occurring isoforms of DNAJ chaperones had opposing effects on HTT-polyQ vs. mutFUS aggregation. We identified a complex of the full length (FL) DNAJB14 and DNAJB12 isoforms which substantially alleviated mutFUS aggregation, in an HSP70-dependent manner. Their naturally occurring short isoforms were unable to form the complex, nor to interact with HSP70, and lost their ability to reduce mutFUS aggregation. In contrast, the short isoform of DNAJB12 significantly alleviated HTT-polyQ aggregation, while DNAJB12-FL aggravated HTT-polyQ aggregation. Finally, we demonstrated that full-length DNAJB14 ameliorated mutFUS aggregation compared to DNAJB14-short in primary neurons. Together, our data unraveled distinct molecular properties required for aggregation protection in different neurodegenerative diseases, and revealed a new layer of complexity of the chaperone network elicited by naturally occurring J-protein isoforms, highlighting functional diversity among the DNAJ family.

molecular biology↗