Evidence map›Paper›PMID 36662373›Full record

ArticleBiogerontology2023

Adult-restricted gene knock-down reveals candidates that affect locomotive healthspan in C. elegans.

Areta Jushaj, Matthew Churgin, Miguel De La Torre, Amanda Kieswetter, Brecht Driesschaert, Ineke Dhondt, Bart P Braeckman, Christopher Fang-Yen, Liesbet Temmerman

Abstract read
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In one paragraph

Article in Biogerontology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 99% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 3 institutions in 2 countries.

Areta JushajAnimal Physiology and Neurobiology, Department of Biology, KU Leuven, Leuven, Belgium.ORCID 0000-0002-7297-7756
Matthew ChurginDepartment of Bioengineering, University of Pennsylvania, Philadelphia, USA.
Miguel De La TorreDepartment of Bioengineering, University of Pennsylvania, Philadelphia, USA.
Amanda KieswetterAnimal Physiology and Neurobiology, Department of Biology, KU Leuven, Leuven, Belgium.
Brecht DriesschaertAnimal Physiology and Neurobiology, Department of Biology, KU Leuven, Leuven, Belgium.
Ineke DhondtLaboratory of Aging Physiology and Molecular Evolution, Department of Biology, Ghent University, Ghent, Belgium.
Bart P BraeckmanLaboratory of Aging Physiology and Molecular Evolution, Department of Biology, Ghent University, Ghent, Belgium.
Christopher Fang-YenDepartment of Bioengineering, University of Pennsylvania, Philadelphia, USA.
Liesbet TemmermanAnimal Physiology and Neurobiology, Department of Biology, KU Leuven, Leuven, Belgium. Liesbet.Temmerman@kuleuven.be.
KU Leuven · BEUniversity of Pennsylvania · USGhent University · BE

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

Understanding how we can age healthily is a challenge at the heart of biogerontological interest. Whereas myriad genes are known to affect the lifespan of model organisms, effects of such interventions on healthspan-the period of life where an animal is considered healthy, rather than merely alive-are less clear. To understand relationships between life- and healthspan, in recent years several platforms were developed with the purpose of assessing both readouts simultaneously. We here relied on one such platform, the WorMotel, to study effects of adulthood-restricted knock-down of 130 Caenorhabditis elegans genes on the locomotive health of the animals along their lifespans. We found that knock-down of six genes affected healthspan while lifespan remained unchanged. For two of these, F26A3.4 and chn-1, knock-down resulted in an improvement of healthspan. In follow-up experiments we showed that knockdown of F26A3.4 indeed improves locomotive health and muscle structure at old age.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsAnimalsGene Knockdown TechniquesLongevityCaenorhabditis elegans ProteinsAgingC. elegansF26A3.4HealthspanLocomotionWorMotel

Identifiers

PMID36662373
OpenAlexW4317566537

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.