Evidence map›Paper›PMID 27053646›Full record

ReviewAmerican journal of physiology. Regulatory, integrative and comparative physiology2016

Mechanisms of animal diapause: recent developments from nematodes, crustaceans, insects, and fish.

Steven C Hand, David L Denlinger, Jason E Podrabsky, Richard Roy

Abstract readReview
In one paragraph

Review in American journal of physiology. Regulatory, integrative and comparative physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 113 papers.

0numbers the graph read from it
0cells of the map it votes in
113citing 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

113 citing papers in PubMed.

  1. Article
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  15. Low oxidative stress during mitochondrial recovery from anoxia in Artemia franciscana, an invertebrate extremophile.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2025
    Article
  16. Review
  17. Article
  18. Biomolecular condensates-Prerequisites for anhydrobiosis?Protein science : a publication of the Protein Society · 2025
    Review
  19. Article
  20. A genome-wide association study implicates the olfactory system inbioRxiv : the preprint server for biology · 2025
    Article

53 more citing papers are in PubMed but not listed here.

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

4 authors.

Steven C HandDepartment of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana; shand@LSU.edu.
David L DenlingerDepartments of Entomology and Evolution, Ecology and Organismal Biology, Ohio State University, Columbus, Ohio;
Jason E PodrabskyDepartment of Biology, Portland State University, Portland, Oregon; and.
Richard RoyDepartment of Biology, McGill University, Montréal, Québec, Canada.

Funding

Heptocellular Response to CryopreservationR01DK046270 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI TONER, MEHMET · 1999 to 2011
$3.4M
The Role of phosphoenolpyruvate carboxykinase and reactive oxygen species in theR01HL095454 · NHLBI · PORTLAND STATE UNIVERSITY · PI PODRABSKY, JASON EARL · 2010 to 2013
$1.4M
Molecular regulation of diapause in Culex pipiensR56AI058279 · NIAID · OHIO STATE UNIVERSITY · PI DENLINGER, DAVID L · 2012 to 2012
$273k
CIHR MOP84486NHLBI NIH HHS R01 HL095454NIAID NIH HHS R56 AI058279NIDDK NIH HHS R01 DK046270
6 · The paper itself

Abstract

Life cycle delays are beneficial for opportunistic species encountering suboptimal environments. Many animals display a programmed arrest of development (diapause) at some stage(s) of their development, and the diapause state may or may not be associated with some degree of metabolic depression. In this review, we will evaluate current advancements in our understanding of the mechanisms responsible for the remarkable phenotype, as well as environmental cues that signal entry and termination of the state. The developmental stage at which diapause occurs dictates and constrains the mechanisms governing diapause. Considerable progress has been made in clarifying proximal mechanisms of metabolic arrest and the signaling pathways like insulin/Foxo that control gene expression patterns. Overlapping themes are also seen in mechanisms that control cell cycle arrest. Evidence is emerging for epigenetic contributions to diapause regulation via small RNAs in nematodes, crustaceans, insects, and fish. Knockdown of circadian clock genes in selected insect species supports the importance of clock genes in the photoperiodic response that cues diapause. A large suite of chaperone-like proteins, expressed during diapause, protects biological structures during long periods of energy-limited stasis. More information is needed to paint a complete picture of how environmental cues are coupled to the signal transduction that initiates the complex diapause phenotype, as well as molecular explanations for how the state is terminated. Excellent examples of molecular memory in post-dauer animals have been documented in Caenorhabditis elegans It is clear that a single suite of mechanisms does not regulate diapause across all species and developmental stages.

Indexed as

Models, BiologicalAnimalsCLOCK ProteinsCrustaceaDiapause, InsectFishesInsectaLife Cycle StagesNematodaSpecies SpecificityCLOCK Proteinscell cycledevelopmentdiapausedormancymetabolism

Identifiers

PMID27053646
PMCPMC4935499

What OpenQuestion holds

Textmetadata
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.