Evidence map›Paper›PMID 29493066›Full record

ArticleAging cell2018

Sex-specific regulation of aging in Caenorhabditis elegans.

Bernadette Hotzi, Mónika Kosztelnik, Balázs Hargitai, Krisztina Takács-Vellai, János Barna, Kincső Bördén, András Málnási-Csizmadia, Mónika Lippai, Csaba Ortutay, Caroline Bacquet and 4 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 33% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  3. Review
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  7. Reproductive Suicide: Similar Mechanisms of Aging inFrontiers in cell and developmental biology · 2021
    Article
  8. Sulforaphane Targets TRA-1/GLI Upstream of DAF-16/FOXO to PromoteFrontiers in cell and developmental biology · 2021
    Article
  9. Review
  10. Article
  11. Article
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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

14 authors at 3 institutions in 3 countries.

Bernadette HotziDepartment of Genetics, Eötvös Loránd University, Budapest, Hungary.
Mónika KosztelnikDepartment of Genetics, Eötvös Loránd University, Budapest, Hungary.
Balázs HargitaiDepartment of Genetics, Eötvös Loránd University, Budapest, Hungary.
Krisztina Takács-VellaiDepartment of Biological Anthropology, Eötvös Loránd University, Budapest, Hungary.
János BarnaDepartment of Genetics, Eötvös Loránd University, Budapest, Hungary.
Kincső BördénDepartment of Genetics, Eötvös Loránd University, Budapest, Hungary.
András Málnási-CsizmadiaDepartment of Biochemistry, Eötvös Loránd University, Budapest, Hungary.
Mónika LippaiDepartment of Anatomy, Cell- and Developmental Biology, Eötvös Loránd University, Budapest, Hungary.
Csaba OrtutayHiDucator Ltd, Kangasala, Finland.
Caroline BacquetInstitute of Enzymology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Angela PasparakiInstitute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, Heraklion, Greece.
Tamás ArányiInstitute of Enzymology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Nektarios TavernarakisInstitute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, Heraklion, Greece.
Tibor VellaiDepartment of Genetics, Eötvös Loránd University, Budapest, Hungary.
Eötvös Loránd University · HUFoundation for Research and Technology Hellas · GRHUN-REN Research Centre for Natural Sciences · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A fascinating aspect of sexual dimorphism in various animal species is that the two sexes differ substantially in lifespan. In humans, for example, women's life expectancy exceeds that of men by 3-7 years. Whether this trait can be attributed to dissimilar lifestyles or genetic (regulatory) factors remains to be elucidated. Herein, we demonstrate that in the nematode Caenorhabditis elegans, the significantly longer lifespan of hermaphrodites-which are essentially females capable of sperm production-over males is established by TRA-1, the terminal effector of the sex-determination pathway. This transcription factor directly controls the expression of daf-16/FOXO, which functions as a major target of insulin/IGF-1 signaling (IIS) and key modulator of aging across diverse animal phyla. TRA-1 extends hermaphrodite lifespan through promoting daf-16 activity. Furthermore, TRA-1 also influences reproductive growth in a DAF-16-dependent manner. Thus, the sex-determination machinery is an important regulator of IIS in this organism. These findings provide a mechanistic insight into how longevity and development are specified unequally in the two genders. As TRA-1 is orthologous to mammalian GLI (glioma-associated) proteins, a similar sex-specific mechanism may also operate in humans to determine lifespan.

Indexed as

AgingAnimalsCaenorhabditis elegansFemaleMaleSex Determination ProcessesSex FactorsagingCaenorhabditis elegansdaf-16/FOXOdauer developmentinsulin/IGF-1 signalingsex determinationTRA-1/GLI

Identifiers

PMID29493066
PMCPMC5946081
OpenAlexW2791945243

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.