A high-throughput assay quantifies thermal scaling of Drosophila development with minute-scale precision
Sobrido-Camean, D.; Claro-Linares, F.; Ruiz-Gomez, N.; Rojas-Rios, P.; Olmedo, M.
Show abstract
Precise regulation of developmental timing is essential for coordinated growth and robust development, yet staging remains technically challenging in many model systems. In Drosophila melanogaster, developmental timing has traditionally been assessed using low-throughput or coarse staging methods, limiting insight into how individual larval stages respond to environmental and genetic perturbations. Here, we present a high-throughput, real-time luminometry assay that enables continuous, automated measurement of postembryonic development in individual Drosophila larvae. By monitoring feeding-dependent luciferase activity, this method reliably detects transitions between larval instars and molts of individual larvae with minute-scale temporal resolution. Using this platform, we provide a quantitative, minute-precision, stage-resolved description of larval development across large cohorts, revealing distinct patterns of variability and weak temporal coupling between stages. We next examine how temperature shapes developmental timing across a broad thermal range. Increasing temperature uniformly accelerates larval development while preserving the proportional contribution of each stage, indicating that the temporal architecture of development is maintained as overall pace changes. Developmental rate follows predictable thermodynamic scaling within a defined temperature window, enabling precise estimation of thermal parameters at both whole-organism and stage-specific levels. Finally, we demonstrate that the assay is compatible with genetic perturbations. This work establishes a scalable, high-precision framework for measuring postembryonic development in Drosophila melanogaster. By revealing the modular and coordinated nature of larval growth, it enables systematic dissection of genetic, metabolic, and environmental control of developmental timing and provides a platform to explore fundamental principles of development and robustness across species.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Distinct neural circuits establish the same chemosensory behavior in C. elegans 94%
- Timed receptor tyrosine kinase signaling couples the central and a peripheral circadian clock in Drosophila 94%
- Dissecting neuron-specific functions of circadian genes using modified cell-specific CRISPR approaches 94%
Similar papers in this journal
Similar papers in this journal
- Molecular encoding of stimulus features in a single sensory neuron type enables neuronal and behavioral plasticity 95%
- Neuronal perception of the social environment intergenerationally controls germline development and generation time in C. elegans 95%
- Interneuron Control of C. elegans Developmental Decision-making 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.