Evidence map›Paper›PMID 42848421›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Cycles upon cycles-Temperature scaling of medaka development.

Sapna Chhabra, Victoria Mochulska, Carina B Vibe, Anubhuti Anushree, Kristina S Stapornwongkul, Thomas Thumberger, Joachim Wittbrodt, Paul François, Alexander Aulehla

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Sapna Chhabra *Developmental Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.ORCID 0000-0002-2479-0911
Victoria Mochulska *Department of Physics, McGill University, Montreal, QC H3A 2T8, Canada.ORCID 0000-0002-1765-6132
Carina B Vibe *Developmental Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.ORCID 0000-0002-6309-269X
Anubhuti AnushreeDevelopmental Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.ORCID 0009-0009-3991-6415
Kristina S StapornwongkulDevelopmental Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.ORCID 0000-0002-7299-9672
Thomas ThumbergerCenter for Organismal Studies, University of Heidelberg, Heidelberg 69120, Germany.ORCID 0000-0001-8485-457X
Joachim WittbrodtCenter for Organismal Studies, University of Heidelberg, Heidelberg 69120, Germany.ORCID 0000-0001-8550-7377
Paul FrançoisDepartement de Biochimie et Médecine Moléculaire, Université de Montréal, Montréal, QC H3T 1J4, Canada.ORCID 0000-0002-2223-839X
Alexander AulehlaDevelopmental Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.ORCID 0000-0003-3487-9239

Funding

EC | European Research Council (ERC) 866537European Molecular Biology Laboratory (EMBL) 847543Fonds de recherche du Québec (FRQ) 328292
6 · The paper itself

Abstract

How organisms develop in dynamic environmental conditions is a fundamental question. We asked how day-night temperature cycles impact embryonic axis elongation and segmentation, itself a cyclic process linked to the segmentation clock, using the Japanese rice fish medaka. We developed an unbiased dimensional reduction approach, based on Singular Value Decomposition, to reliably identify the dynamic modes of segmentation clock oscillations across all temperature conditions. We reveal that the two major dynamic modes show opposite temperature sensitivities: While the temporal oscillation (mode 1) varies strongly with temperature, the spatial phase gradient (mode 2) appears largely temperature invariant. In addition, we found developmental parameters with intermediate, subscaled temperature responses, such as axis elongation. We used theoretical modeling to understand how dynamic modes emerge from the underlying local oscillation dynamics and axis elongation. We then exposed embryos to circadian and ultradian temperature cycles to reveal dynamic response patterns of oscillations and axis elongation, and found how these responses are integrated into morphological features. Combined, our theoretical-experimental results support a model in which the dynamic integration of temporal (i.e. segmentation clock related) and spatial (i.e. axis elongation) processes, in particular their subscaled temperature response patterns, quantitatively compensate each other to yield a robust, temperature-invariant axis patterning outcome.

Indexed as

OryziasTemperatureAnimalsBody PatterningCircadian RhythmEmbryonic DevelopmentEmbryo, NonmammalianModels, Biologicaldevelopmental modularitysegmentation clockSingular Value Decompositiontemperature scaling

Identifiers

PMID42848421
PMCPMC13663819

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.