Evidence map›Paper›PMID 26568616›Full record

ArticleMolecular biology and evolution2016

Global Transcriptional Profiling of Diapause and Climatic Adaptation in Drosophila melanogaster.

Xiaqing Zhao, Alan O Bergland, Emily L Behrman, Brian D Gregory, Dmitri A Petrov, Paul S Schmidt

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.6field-weighted citation impact, top 4% of its field
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

24 citing papers in PubMed, 71 citations in OpenAlex.

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  6. Altered circadian rhythm, sleep, andProceedings of the National Academy of Sciences of the United States of America · 2024
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  17. Review
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  19. Review
  20. Non-model model organisms.BMC biology · 2017
    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

6 authors at 2 institutions in 1 country.

Xiaqing ZhaoDepartment of Biology, University of Pennsylvania xiaqing@sas.upenn.edu.
Alan O BerglandDepartment of Biology, Stanford University.
Emily L BehrmanDepartment of Biology, University of Pennsylvania.
Brian D GregoryDepartment of Biology, University of Pennsylvania.
Dmitri A PetrovDepartment of Biology, Stanford University.
Paul S SchmidtDepartment of Biology, University of Pennsylvania.
University of Pennsylvania · USStanford University · US

Funding

Genomics of rapid adaptation on seasonal timescales in D. melanogasterR01GM100366 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI SCHMIDT, PAUL · 2012 to 2019
$3.3M
NIGMS NIH HHS R01 GM100366
6 · The paper itself

Abstract

Wild populations of the model organism Drosophila melanogaster experience highly heterogeneous environments over broad geographical ranges as well as over seasonal and annual timescales. Diapause is a primary adaptation to environmental heterogeneity, and in D. melanogaster the propensity to enter diapause varies predictably with latitude and season. Here we performed global transcriptomic profiling of naturally occurring variation in diapause expression elicited by short day photoperiod and moderately low temperature in two tissue types associated with neuroendocrine and endocrine signaling, heads, and ovaries. We show that diapause in D. melanogaster is an actively regulated phenotype at the transcriptional level, suggesting that diapause is not a simple physiological or reproductive quiescence. Differentially expressed genes and pathways are highly distinct in heads and ovaries, demonstrating that the diapause response is not uniform throughout the soma and suggesting that it may be comprised of functional modules associated with specific tissues. Genes downregulated in heads of diapausing flies are significantly enriched for clinally varying single nucleotide polymorphism (SNPs) and seasonally oscillating SNPs, consistent with the hypothesis that diapause is a driving phenotype of climatic adaptation. We also show that chromosome location-based coregulation of gene expression is present in the transcriptional regulation of diapause. Taken together, these results demonstrate that diapause is a complex phenotype actively regulated in multiple tissues, and support the hypothesis that natural variation in diapause propensity underlies adaptation to spatially and temporally varying selective pressures.

Indexed as

ClimateGene Expression ProfilingTranscriptomeAdaptation, BiologicalAnimalsChromosome MappingComputational BiologyDiapause, InsectDrosophila melanogasterGene-Environment InteractionGene Expression RegulationGene OntologyMolecular Sequence AnnotationSeasonsclimatic adaptationdiapauseDrosophila melanogasterRNAseq

Identifiers

PMID26568616
PMCPMC5009998
OpenAlexW2176422404

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.