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Augustine, F.

Publications and source records attributed to Augustine, F..

3 recordsLinked to original sources

BehaviorScope-X: reusing pose-trained visual representations for full-video ethology

Pose-estimation pipelines usually export keypoint coordinates and discard the intermediate visual representations learned to localize animals in a specific assay. We asked whether those discarded representations can be reused for full-video ethology. BehaviorScope-X tests this idea by treating a trained pose checkpoint as both a keypoint estimator and a reusable visual encoder: the pose model is run once to cache detections, keypoints, pose-derived social geometry, and frozen intermediate descriptors, after which compact temporal classifiers are trained on cached multimodal windows. Across MARS resident-intruder videos, cached pose-trained descriptors and pose-derived geometry provided complementary evidence for behavior decoding, recovering sustained behavioral episodes and local sequence structure while revealing a main limitation in dense short-bout regions. The same cache-and-classify design generalized across pose routes, including a MobileNetV3 backbone and a DeepLabCut SuperAnimal HRNet-W32 checkpoint, showing that standard pose workflows can expose behavior-relevant visual descriptors without giving up their keypoint-estimation role. We further tested the approach in Fly-v-Fly aggression, extending the analysis to a second species and shorter behavioral time scale, where sub-second events and annotation-boundary uncertainty limited strict bout recovery. End-to-end profiling showed that the workflow can operate near-real-time or real-time on consumer hardware. Together, these experiments support amortized pose vision as a practical strategy for reusing assay-trained pose models as stable sources of visual and geometric evidence for scalable behavioral analysis. Author summaryPose-estimation models are usually used to convert animal video into body landmarks, while the same models internal visual representations are discarded. We ask whether the model that estimates pose can also provide visual features for behavior analysis. Our workflow runs a trained pose model once, caches its landmarks, pose-derived interaction geometry, and internal visual features, and trains compact behavior classifiers on that cache. Across multiple pose backbones and pose-estimation workflows, these shared pose-and-visual signals supported full-video ethogram recovery without training a separate video network. This turns pose training into a reusable source of assay-specific visual and geometric evidence for scalable behavioral analysis. HighlightsO_LIA pose-estimation checkpoint is reused as both keypoint estimator and visual encoder. C_LIO_LIA single pose-inference pass caches keypoints, social geometry, and intermediate visual descriptors. C_LIO_LICached pose-derived visual and geometric evidence improves full-video behavior decoding beyond pose-derived features alone. C_LIO_LIBehaviorScope-X turns existing pose workflows into reusable full-video behavior-analysis pipelines. C_LI

neuroscience↗

Functional regulation of 4D metabolic network between multienzyme glucosome condensates and mitochondria

Glucose metabolism is biochemically intertwined between energy metabolism and building block biosynthesis in living cells. However, it has not been investigated yet how its metabolic network is orchestrated to govern glucose flux in space and time. Since we reported that human enzymes in glucose metabolism are spatially organized into metabolically active membraneless compartments (i.e., glucosomes), we have employed lattice light sheet microscopic imaging and other biophysical and biochemical techniques to understand their functional significance in cellular metabolism. Now, we demonstrated that glucosome assemblies behave like liquid droplets in human cells and thus reversibly respond to environmental changes. In addition, we characterized a molecular architecture of the glucosome, which appears to be constructed from higher-ordered oligomeric structures of its scaffolder enzyme along with transient enzyme-enzyme interactions. Importantly, we found that enzymatic compositions of glucosomes are altered when they are spatially in proximity to mitochondria to functionally couple glycolysis with mitochondrial metabolism in human cells. Collectively, we envision that the subcellular localization-function relationship between glucosomes and mitochondria may represent one of fundamental principles by which 4-dimensional metabolic networks are not only dynamically but also efficiently regulated in living human cells. One Sentence SummaryInvestigation of a 4D functional network of glucose metabolism uncovers a fundamental principal of subcellular metabolic regulation in human cells.

biochemistry↗

Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify candidate risk genes and biological pathways

Motor stereotypies are common in children with autism spectrum disorder (ASD), intellectual disability, or sensory deprivation, as well as in typically developing children (\"primary\" stereotypies, CMS). The precise pathophysiological mechanism for motor stereotypies is unknown, although genetic etiologies have been suggested. In this study, we perform whole-exome DNA sequencing in 129 parent-child trios with CMS and 853 control trios (118 cases and 750 controls after quality control). We report an increased rate of de novo predicted-damaging variants in CMS versus controls, identifying KDM5B as a high-confidence risk gene and estimating 184 genes conferring risk. Genes harboring de novo damaging variants in CMS probands show significant overlap with those in Tourette syndrome, ASD candidate genes, and those in ASD probands with high stereotypy scores. Furthermore, exploratory biological pathway and gene ontology analysis highlight histone demethylation, organism development, cell motility, glucocorticoid receptor pathway, and ion channel transport. Continued sequencing of CMS trios will identify more risk genes and allow greater insights into biological mechanisms of stereotypies across diagnostic boundaries.

genomics↗