Daniel T. Choe
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Daniel T. Choe has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- J. Alexander Bae
Princeton Neuroscience Institute, Princeton University, Princeton, USA
2 shared publications - Junho Lee
Department of Biological Sciences, Seoul National University, Seoul 08826, Korea
2 shared publications David H Hall
Yeshiva University Albert Einstein College of Medicine
1 shared publication- David H. Hall
Affiliation Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, United States of America
1 shared publication Gwanho Ko
Department of Biological Sciences Seoul National University Seoul 08826 Republic of Korea
1 shared publication- Hyunsoo Yim
Department of Biological Sciences, Howard Hughes Medical Institute, Columbia University
1 shared publication
Latest Publications
- Open Access
Comparative connectomics reveals stage-specific gap junction rewiring that reshapes avoidance behavior
Environmental stress can remodel neural circuits, yet how such rewiring generates behavioral adaptation remains poorly understood. Here, we investigated how dauer-specific circuit remodeling alters nociceptive behavior. We discovered that dauers exhibit significantly shorter avoidance durations than adults. Through comparative connectomics, we observed a substantial expansion of gap junctions within the dauer nociceptive circuit and found that dauer neurons exhibit more transient activity dynamics as a result of this rewiring. Modeling neuronal activity demonstrated that removing dauer-specific connectivity constraints failed to reproduce transient characteristics, validating the functional role of dauer-specific gap junctions. Furthermore, introducing synthetic dauer-specific gap junctions into adults was sufficient to recapitulate dauer-like activity patterns and shorten avoidance duration. Despite extensive rewiring, avoidance initiation remained preserved across developmental stages. Our findings show that the dauer neural circuit is selectively rewired through gap junction remodeling to balance flexibility and stability for survival under stress.
Open AccessComparative connectomics reveals stage-specific gap junction rewiring that reshapes avoidance behavior
Environmental stress can remodel neural circuits, yet how such rewiring generates behavioral adaptation remains poorly understood. Here, we investigated how dauer-specific circuit remodeling alters nociceptive behavior. We discovered that dauers exhibit significantly shorter avoidance durations than adults. Through comparative connectomics, we observed a substantial expansion of gap junctions within the dauer nociceptive circuit and found that dauer neurons exhibit more transient activity dynamics as a result of this rewiring. Modeling neuronal activity demonstrated that removing dauer-specific connectivity constraints failed to reproduce transient characteristics, validating the functional role of dauer-specific gap junctions. Furthermore, introducing synthetic dauer-specific gap junctions into adults was sufficient to recapitulate dauer-like activity patterns and shorten avoidance duration. Despite extensive rewiring, avoidance initiation remained preserved across developmental stages. Our findings show that the dauer neural circuit is selectively rewired through gap junction remodeling to balance flexibility and stability for survival under stress.
- Open Access
- 6 March 2025
- Published by Wiley in Advanced Science
- Vol. 12 (20) , e2411191
Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy
As an animal matures, its neural circuit undergoes alterations, yet the developmental changes in intracellular organelles to facilitate these changes is less understood. Using 3D electron microscopy and deep learning, the study develops semi‐automated methods for reconstructing mitochondria in C . elegans and collected mitochondria reconstructions from normal reproductive stages and dauer, enabling comparative study on mitochondria structure within the neuromuscular system. It is found that various mitochondria structural properties in neurons correlate with synaptic connections and these properties are preserved across development in different neural circuits. To test the necessity of these universal mitochondria properties, the study examines the behavior in drp‐1 mutants with impaired mitochondria fission and discovers that it causes behavioral deficits. Moreover, it is observed that dauer neurons display distinctive mitochondrial features, and mitochondria in dauer muscles exhibit unique reticulum‐like structure. It is proposed that these specialized mitochondria structures may serve as an adaptive mechanism to support stage‐specific behavioral and physiological needs.
- 6 March 2025
- Published by Wiley in Advanced Science
- Vol. 12 (20) , e2411191
Open AccessStructural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy
As an animal matures, its neural circuit undergoes alterations, yet the developmental changes in intracellular organelles to facilitate these changes is less understood. Using 3D electron microscopy and deep learning, the study develops semi‐automated methods for reconstructing mitochondria in C . elegans and collected mitochondria reconstructions from normal reproductive stages and dauer, enabling comparative study on mitochondria structure within the neuromuscular system. It is found that various mitochondria structural properties in neurons correlate with synaptic connections and these properties are preserved across development in different neural circuits. To test the necessity of these universal mitochondria properties, the study examines the behavior in drp‐1 mutants with impaired mitochondria fission and discovers that it causes behavioral deficits. Moreover, it is observed that dauer neurons display distinctive mitochondrial features, and mitochondria in dauer muscles exhibit unique reticulum‐like structure. It is proposed that these specialized mitochondria structures may serve as an adaptive mechanism to support stage‐specific behavioral and physiological needs.