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Biology subjects

Heo, G.

Publications and source records attributed to Heo, G..

3 recordsLinked to original sources

Spectral envelopes of rhythmic facial movements predict intention and motor cortical representations

1Animals, including humans, use coordinated facial movements to sample the environment, ingest nutrients, and communicate. Rodents, in particular, produce rhythmic facial movements during spontaneous behavior and cognitive tasks. Measuring these movements precisely and linking them to neural activity remains challenging. We introduce face-rhythm, an unsupervised pipeline that combines markerless pointtracking, spectral analysis, and non-negative tensor component analysis to decompose facial video into a small set of interpretable components. Applied to videos of mice during a Pavlovian odor-reward task, a brain-machine interface (BMI) task, and free behavior, face-rhythm recovers human-interpretable behaviors such as whisking, sniffing, licking, and subtler motifs. The resulting components are consistent across animals, are sufficient to decode task variables or internal belief states, and explain cortical activity using a low-rank representation. We also find that the activity of neurons in face-associated primary motor cortex (M1) is predicted well by a phase-invariant spectral transformation of facial movements above [~]0.5 Hz, while slower movements retain a phase-variant representation better predicted by the instantaneous position of the face; individual neurons can show either or both forms of tuning. A systematic comparison against deeplearning point-tracking models, contrastive-learning embeddings, and vision-transformer features places face-rhythm competitively across tasks while also achieving the goal of producing a low-dimensional, interpretable description of rodent facial behavior that is closely linked to cortical activity.

neuroscience↗

High-Throughput Glycan Array Screening Reveals Rhamnogalacturonan-I as a Ligand for Arabidopsis Leucine-Rich Repeat Receptor Kinases

The plant cell wall not only serves as a physical barrier against pathogens but, when damaged, also functions as a source of cell wall-derived molecules that play crucial roles in plant immunity as damage-associated molecular patterns (DAMPs). While oligogalacturonides from homogalacturonan are well-studied DAMPs, the immune-signaling potential of other cell wall components remains largely unexplored. Conventional genetic and biochemical approaches aimed at identifying ligand-receptor pairs in plant immunity have been limited by the vast diversity of potential ligand molecules and functional redundancy of putative receptors. Here, we developed a high-throughput screening pipeline that simultaneously examines multiple interactions between plant cell wall-derived glycans and >350 extracellular domains (ECDs) of receptor kinases and receptor like proteins in Arabidopsis, resulting in the screening of >40,000 interactions. We discovered a group of leucine-rich repeat receptor kinases named ARMs (AWARENESS of RG-I MAINTENANCES) that interact with rhamnogalacturonan-I (RG-I), a major component of pectin. RG-I treatment induced pattern-triggered immunity responses, with distinct kinetics compared to oligogalacturonide responses. We identified RG-I oligosaccharide structures required for interaction with ARM receptors and immune activation, and found that ARM receptors are redundantly involved in plant immunity. Collectively, our approach provides a powerful platform for discovering glycan-receptor pairs in plants, facilitating a more comprehensive understanding of cell wall surveillance mechanisms in plant immunity.

plant biology↗

Mature leaves produce a multi-layered wound periderm by integrating phytohormone signaling with ATML1-mediated epidermal specification

The epidermis of plants forms a protective barrier against various stress, but how breaches in the epidermis are repaired is not well understood. Here, we investigated wound healing in the mature leaves of Arabidopsis. We discover a novel type of wound periderm comprising a multi-layered ligno-suberized barrier covered with cuticular wax, which is formed by mesophyll cells that adopt an epidermal fate. Mesophyll cells of protective layer 1 (P1), just beneath the wound, transition into epidermal cells, which seal the wound by depositing cuticle. As P1 undergoes cell death, protective layer 2 (P2), which underlies P1, takes the place of P1 and undergoes ligno-suberization. This multi-layered periderm involves integration of ethylene and jasmonic acid signaling with ATML1, a key transcription factor in epidermal specification, to coordinate cell layer-specific functions. This novel wound periderm also occurs in the leaves of tobacco and Capsella, suggesting it is a widespread phenomenon.

plant biology↗