DynamicAtlas: a morphodynamic atlas for Drosophila development

Living organisms develop their shape through the interplay of gene expression and mechanics. While atlases of static samples characterize cell fates and gene regulation, understanding dynamic shape changes requires live imaging. Here we present DynamicAtlas: a 'morphodynamic atlas' of live and static datasets from 500 Drosophila melanogaster embryos (wild type and 18 mutants), aligned to a common morphological timeline. Surprisingly, characterizing wild-type surface tissue flows reveals distinct 'morphodynamic modules'-time periods in which the global pattern of motion is stationary-corresponding to key developmental stages. Mutant analysis shows stationary flow patterns depend on genes that break spatial symmetry along the dorsal-ventral axis. Temperature perturbations indicate that morphodynamic modules change in response to accumulated tissue deformation, rather than elapsed time. Extending our approach to the embryonic Drosophila midgut, we find modules in covariant measures of the dynamic three-dimensional surface. DynamicAtlas provides a high-resolution framework for studying shape formation across living systems.

Authors

Institutions

Publication Details

Journal
Nature Methods
Published
2025-12-24
DOI
https://doi.org/10.1038/s41592-025-02897-8
Citations
1
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
1.15
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

DynamicAtlas: a morphodynamic atlas for Drosophila development

Nikolas H Claussen, Andreas R. Bausch, Marion K Raich, Noah Mitchell et al.
1 citations
Nature Methods
Cellular Mechanics and Interactions
1.15
article

DynamicAtlas: a morphodynamic atlas for Drosophila development

Nikolas H Claussen, Andreas R. Bausch, Marion K Raich, Noah Mitchell, Hannah J. Gustafson, Matthew F Lefebvre, Sebastian J. Streichan, Vishank Jain-Sharma, Friederike E. Streichan
article en
1 citations

Abstract

Living organisms develop their shape through the interplay of gene expression and mechanics. While atlases of static samples characterize cell fates and gene regulation, understanding dynamic shape changes requires live imaging. Here we present DynamicAtlas: a 'morphodynamic atlas' of live and static datasets from 500 Drosophila melanogaster embryos (wild type and 18 mutants), aligned to a common morphological timeline. Surprisingly, characterizing wild-type surface tissue flows reveals distinct 'morphodynamic modules'-time periods in which the global pattern of motion is stationary-corresponding to key developmental stages. Mutant analysis shows stationary flow patterns depend on genes that break spatial symmetry along the dorsal-ventral axis. Temperature perturbations indicate that morphodynamic modules change in response to accumulated tissue deformation, rather than elapsed time. Extending our approach to the embryonic Drosophila midgut, we find modules in covariant measures of the dynamic three-dimensional surface. DynamicAtlas provides a high-resolution framework for studying shape formation across living systems.

Nature MethodsVol. 23(1)
University of California, Santa Barbara (US), University of Chicago (US), Quantitative BioSciences (US), Max Planck Institute of Psychiatry (DE), Technical University of Munich (DE)
Openalex Percentile: Top 17%
Cellular Mechanics and Interactions
1.15
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.