Evidence map›Paper›PMID 37118502›Full record

ArticleNature aging2022

Males induce premature demise of the opposite sex by multifaceted strategies.

Lauren N Booth, Cheng Shi, Cindy Tantilert, Robin W Yeo, Jason W Miklas, Katja Hebestreit, Cecilia N Hollenhorst, Travis J Maures, Matthew T Buckley, Coleen T Murphy and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Nature aging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Acyl-CoA-binding protein as a driver of pathological aging.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Article
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  10. Article
  11. Article
  12. Review
  13. AbioRxiv : the preprint server for biology · 2023
    Article
  14. Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Lauren N BoothDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Cheng ShiDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA.ORCID 0000-0003-0365-8273
Cindy TantilertDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Robin W YeoDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Jason W MiklasDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-9002-0667
Katja HebestreitDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Cecilia N HollenhorstDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-1135-757X
Travis J MauresDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Matthew T BuckleyDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Coleen T MurphyDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA. ctmurphy@princeton.edu.ORCID 0000-0002-8257-984X
Anne BrunetDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA. abrunet1@stanford.edu.ORCID 0000-0002-4608-6845
Stanford University · USPrinceton University · USEnzo Life Sciences (United States) · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Link between epigenetic modifiers and fat metabolism for healthy agingR01AG054201 · NIA · STANFORD UNIVERSITY · PI BRUNET, ANNE, MAIR, WILLIAM B · 2016 to 2020
$2.2M
Epigenetic Regulation of Longevity in Response to Environmental SignalsK99AG051738 · NIA · STANFORD UNIVERSITY · PI BOOTH, LAUREN NICOLE · 2016 to 2017
$201k
NIA NIH HHS K99 AG051738NIA NIH HHS R01 AG054201NIH HHS P40 OD010440
6 · The paper itself

Abstract

Interactions between the sexes negatively impact health in many species. In Caenorhabditis, males shorten the lifespan of the opposite sex-hermaphrodites or females. Here we use transcriptomic profiling and targeted screens to systematically uncover conserved genes involved in male-induced demise in C. elegans. Some genes (for example, delm-2, acbp-3), when knocked down, are specifically protective against male-induced demise. Others (for example, sri-40), when knocked down, extend lifespan with and without males, suggesting general mechanisms of protection. In contrast, many classical long-lived mutants are impacted more negatively than wild type by the presence of males, highlighting the importance of sexual environment for longevity. Interestingly, genes induced by males are triggered by specific male components (seminal fluid, sperm and pheromone), and manipulating these genes in combination in hermaphrodites induces stronger protection. One of these genes, the conserved ion channel delm-2, acts in the nervous system and intestine to regulate lipid metabolism. Our analysis reveals striking differences in longevity in single sex versus mixed sex environments and uncovers elaborate strategies elicited by sexual interactions that could extend to other species.

Indexed as

CaenorhabditisDisorders of Sex DevelopmentAnimalsCaenorhabditis elegansFemaleLongevityMaleSemenSpermatozoa

Identifiers

PMID37118502
PMCPMC10154206
OpenAlexW4296205049

What OpenQuestion holds

Textmetadata
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.