Evidence map›Paper›PMID 26341296›Full record

ArticleMolecular biology and evolution2015

Transcriptomic Signatures Mirror the Lack of the Fecundity/Longevity Trade-Off in Ant Queens.

Katharina von Wyschetzki, Olav Rueppell, Jan Oettler, Jürgen Heinze

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.9field-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

30 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. The pace and shape of ant ageing.Biological reviews of the Cambridge Philosophical Society · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. TheFrontiers in molecular biosciences · 2022
    Article
  10. Article
  11. Article
  12. Reproductive activation in honeybee (Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Article
  13. Molecular regulation of lifespan extension in fertile ant workers.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Article
  14. The plasticity of lifespan in social insects.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Simple Comparative Analyses of Differentially Expressed Gene Lists May Overestimate Gene Overlap.Journal of computational biology : a journal of computational molecular cell biology · 2018
    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

4 authors at 2 institutions in 2 countries.

Katharina von WyschetzkiLS Zoologie/Evolutionsbiologie, Universität Regensburg, Regensburg, Germany katharina.wyschetzki@ur.de.
Olav RueppellDepartment of Biology, University of North Carolina, Greensboro.
Jan OettlerLS Zoologie/Evolutionsbiologie, Universität Regensburg, Regensburg, Germany.
Jürgen HeinzeLS Zoologie/Evolutionsbiologie, Universität Regensburg, Regensburg, Germany.
University of Regensburg · DEUniversity of North Carolina at Greensboro · US

Funding

Biodemography and Genomics of Aging Trajectories and Plasticity in a Social ModelR21AG046837 · NIA · UNIVERSITY OF NORTH CAROLINA GREENSBORO · PI RUEPPELL, OLAV · 2013 to 2014
$287k
NIA NIH HHS R21 AG046837NIA NIH HHS R21AG046837
6 · The paper itself

Abstract

Life-history theory predicts a trade-off between reproductive investment and self-maintenance. The negative association between fertility and longevity found throughout multicellular organisms supports this prediction. As an important exception, the reproductives of many eusocial insects (ants, bees, and termites) are simultaneously very long-lived and highly fertile. Here, we examine the proximate basis for this exceptional relationship by comparing whole-body transcriptomes of differently aged queens of the ant Cardiocondyla obscurior. We show that the sets of genes differentially expressed with age significantly overlap with age-related expression changes previously found in female Drosophila melanogaster. We identified several developmental processes, such as the generation of neurons, as common signatures of aging. More generally, however, gene expression in ant queens and flies changes with age mainly in opposite directions. In contrast to flies, reproduction-associated genes were upregulated and genes associated with metabolic processes and muscle contraction were downregulated in old relative to young ant queens. Furthermore, we searched for putative C. obscurior longevity candidates associated with the previously reported lifespan-prolonging effect of mating by comparing the transcriptomes of queens that differed in mating and reproductive status. We found 21 genes, including the putative aging candidate NLaz (an insect homolog of APOD), which were consistently more highly expressed in short-lived, unmated queens than in long-lived, mated queens. Our study provides clear evidence that the alternative regulation of conserved molecular pathways that mediate the interplay among mating, egg laying, and aging underlies the lack of the fecundity/longevity trade-off in ant queens.

Indexed as

Age FactorsAnimalsAntsFemaleFertilityLongevityMaleReproductionSexual Behavior, AnimalTranscriptomeagingfecundity/longevity trade-offmatingRNA-Seqsocial insecttranscriptome

Identifiers

PMID26341296
PMCPMC5009957
OpenAlexW2127601203

What OpenQuestion holds

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Registered trials

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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.