Evidence map›Paper›PMID 31316054›Full record

ArticleNature communications2019

The longevity-promoting factor, TCER-1, widely represses stress resistance and innate immunity.

Francis R G Amrit, Nikki Naim, Ramesh Ratnappan, Julia Loose, Carter Mason, Laura Steenberge, Brooke T McClendon, Guoqiang Wang, Monica Driscoll, Judith L Yanowitz and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. 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
1.8field-weighted citation impact, top 18% 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, 68 citations in OpenAlex.

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  19. The molecular tug of war between immunity and fertility: Emergence of conserved signaling pathways and regulatory mechanisms.BioEssays : news and reviews in molecular, cellular and developmental biology · 2020
    Review
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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

11 authors at 2 institutions in 1 country.

Francis R G AmritDepartments of Pediatrics, Developmental Biology and Cell Biology and Physiology, University of Pittsburgh School of Medicine; John G. Rangos Sr. Research Center, Room 7129, One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.ORCID http://orcid.org/0000-0003-1928-3234
Nikki NaimDepartments of Pediatrics, Developmental Biology and Cell Biology and Physiology, University of Pittsburgh School of Medicine; John G. Rangos Sr. Research Center, Room 7129, One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.ORCID http://orcid.org/0000-0002-2005-7202
Ramesh RatnappanDepartments of Pediatrics, Developmental Biology and Cell Biology and Physiology, University of Pittsburgh School of Medicine; John G. Rangos Sr. Research Center, Room 7129, One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
Julia LooseDepartments of Pediatrics, Developmental Biology and Cell Biology and Physiology, University of Pittsburgh School of Medicine; John G. Rangos Sr. Research Center, Room 7129, One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
Carter MasonDepartments of Pediatrics, Developmental Biology and Cell Biology and Physiology, University of Pittsburgh School of Medicine; John G. Rangos Sr. Research Center, Room 7129, One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
Laura SteenbergeDepartments of Pediatrics, Developmental Biology and Cell Biology and Physiology, University of Pittsburgh School of Medicine; John G. Rangos Sr. Research Center, Room 7129, One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
Brooke T McClendonMagee-Womens Research Institute, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Guoqiang WangDepartment of Molecular Biology and Biochemistry, Rutgers, The State University of New York, Nelson Biological Labs, Room A232, Piscataway, NJ, 08854, USA.
Monica DriscollDepartment of Molecular Biology and Biochemistry, Rutgers, The State University of New York, Nelson Biological Labs, Room A232, Piscataway, NJ, 08854, USA.
Judith L YanowitzMagee-Womens Research Institute, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Arjumand GhaziDepartments of Pediatrics, Developmental Biology and Cell Biology and Physiology, University of Pittsburgh School of Medicine; John G. Rangos Sr. Research Center, Room 7129, One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA. Arjumand.Ghazi@chp.edu.ORCID http://orcid.org/0000-0002-5859-4206
University of Pittsburgh · USRutgers, The State University of New Jersey · US

Funding

The Coordination of Lipid Synthesis and Breakdown in Metabolism and AgingR01AG051659 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GHAZI, ARJUMAND · 2016 to 2019
$1.6M
NIA NIH HHS R01 AG051659U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R01AG051659
6 · The paper itself

Abstract

Stress resistance and longevity are positively correlated but emerging evidence indicates that they are physiologically distinct. Identifying factors with distinctive roles in these processes is challenging because pro-longevity genes often enhance stress resistance. We demonstrate that TCER-1, the Caenorhabditis elegans homolog of human transcription elongation and splicing factor, TCERG1, has opposite effects on lifespan and stress resistance. We previously showed that tcer-1 promotes longevity in germline-less C. elegans and reproductive fitness in wild-type animals. Surprisingly, tcer-1 mutants exhibit exceptional resistance against multiple stressors, including infection by human opportunistic pathogens, whereas, TCER-1 overexpression confers immuno-susceptibility. TCER-1 inhibits immunity only during fertile stages of life. Elevating its levels ameliorates the fertility loss caused by infection, suggesting that TCER-1 represses immunity to augment fecundity. TCER-1 acts through repression of PMK-1 as well as PMK-1-independent factors critical for innate immunity. Our data establish key roles for TCER-1 in coordinating immunity, longevity and fertility, and reveal mechanisms that distinguish length of life from functional aspects of aging.

Indexed as

AgingAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsDisease SusceptibilityFertilityGene Expression RegulationImmunity, InnateLongevityMitogen-Activated Protein KinasesModels, AnimalMutationPeptide Elongation FactorsStress, PhysiologicalCaenorhabditis elegans ProteinsMitogen-Activated Protein KinasesPeptide Elongation FactorsPmk-1 protein, C elegansTCER-1 protein, C elegans

Identifiers

PMID31316054
PMCPMC6637209
OpenAlexW2958220721

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.