Evidence map›Paper›PMID 40829645›Full record

ReviewOpen biology2025

Using diapause as a platform to understand the biology of dormancy.

Nathaniel A Sweet, Chi-Kuo Hu

Abstract readReview
In one paragraph

Review in Open biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Killiverse: an interactive multi-omics web resource for killifish.bioRxiv : the preprint server for biology · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Nathaniel A SweetDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY, USA.ORCID 0000-0003-1826-1236
Chi-Kuo HuDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY, USA.ORCID 0000-0002-9773-972X

Funding

Understanding diapause and its ability to suspend and preserve lifeDP2AG077431 · NIA · STATE UNIVERSITY NEW YORK STONY BROOK · PI HU, CHI-KUO · 2021 to 2024
$2.4M
Training Program in Pharmacological SciencesT32GM144304 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI HOLLY A COLOGNATO · 2022 to 2026
$1.8M
Healthy Aging Award of the Center for Healthy Aging at Stony Brook 1186757-98196NIA NIH HHS DP2 AG077431NIGMS NIH HHS T32 GM144304
6 · The paper itself

Abstract

Diapause is a fascinating form of biological dormancy that is employed by a broad array of animals as a survival strategy to endure adverse environmental conditions. This unique dormant state can suspend organismal development until a more favourable condition arises, giving the species the greatest chance to survive as a whole. Remarkably, while following the same principle of suspending development, diapause exists in different forms and can occur at various stages before reaching the adult form. Functionally, with multiple evolutionary origins across the animal kingdom, diapause demonstrates the ability to respond to diverse environmental challenges while converging to maintain the same core function of suspending development. At the physiological level, these different diapause states share a similar metabolic adaptation to conserve resources and energy throughout dormancy. Underneath, the same genes have been repeatedly identified as regulators and effectors of diapause at different developmental stages in both invertebrates and vertebrates. This suggests the presence of a conserved molecular programme comprised of the same set of key genes repeatedly reprogrammed and utilized at the core of diapause. The knowledge of diapause from the organismal to molecular levels, together, should serve as a useful window to better understand the biology of dormancy.

Indexed as

DiapauseAdaptation, PhysiologicalAnimalsBiological EvolutionGene Expression Regulation, DevelopmentalInvertebratesdevelopmental suspensiondiapausedormancymetabolic depression

Identifiers

PMID40829645
PMCPMC12364575

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.