Evidence map›Paper›PMID 28105938›Full record

ArticleBMC genomics2016

The influence of pro-longevity gene Gclc overexpression on the age-dependent changes in Drosophila transcriptome and biological functions.

Alexey Moskalev, Mikhail Shaposhnikov, Ekaterina Proshkina, Alexey Belyi, Alexander Fedintsev, Svetlana Zhikrivetskaya, Zulfiya Guvatova, Asiya Sadritdinova, Anastasia Snezhkina, George Krasnov and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. 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
1.6field-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

13 citing papers in PubMed, 26 citations in OpenAlex.

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  8. The Neuronal Overexpression ofFrontiers in genetics · 2019
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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 4 institutions in 1 country.

Alexey MoskalevEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia. amoskalev@list.ru.
Mikhail ShaposhnikovInstitute of Biology of Komi Science Center of Ural Branch of RAS, Syktyvkar, Russia.
Ekaterina ProshkinaInstitute of Biology of Komi Science Center of Ural Branch of RAS, Syktyvkar, Russia.
Alexey BelyiInstitute of Biology of Komi Science Center of Ural Branch of RAS, Syktyvkar, Russia.
Alexander FedintsevMoscow Institute of Physics and Technology, Dolgoprudny, Russia.
Svetlana ZhikrivetskayaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Zulfiya GuvatovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Asiya SadritdinovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Anastasia SnezhkinaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
George KrasnovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Anna KudryavtsevaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia. rhizamoeba@mail.ru.
Engelhardt Institute of Molecular Biology · RUInstitute of Chemistry, Komi Science Center · RUMoscow Institute of Physics and Technology · RUSyktyvkar State University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTranscriptional changes that contribute to the organism's longevity and prevent the age-dependent decline of biological functions are not well understood. Here, we overexpressed pro-longevity gene encoding glutamate-cysteine ligase catalytic subunit (Gclc) and analyzed age-dependent changes in transcriptome that associated with the longevity, stress resistance, locomotor activity, circadian rhythmicity, and fertility.

resultsHere we reproduced the life extension effect of neuronal overexpression of the Gclc gene and investigated its influence on the age-depended dynamics of transcriptome and biological functions such as fecundity, spontaneous locomotor activity and circadian rhythmicity, as well as on the resistance to oxidative, proteotoxic and osmotic stresses. It was shown that Gclc overexpression reduces locomotor activity in the young and middle ages compared to control flies. Gclc overexpression slowed down the age-dependent decline of locomotor activity and circadian rhythmicity, and resistance to stress treatments. Gclc level demonstrated associations with the expression of genes involved in a variety of cellular processes including Jak-STAT, MAPK, FOXO, Notch, mTOR, TGF-beta signaling pathways, translation, protein processing in endoplasmic reticulum, proteasomal degradation, glycolysis, oxidative phosphorylation, apoptosis, regulation of circadian rhythms, differentiation of neurons, synaptic plasticity and transmission.

conclusionsOur study revealed that Gclc overexpression induces transcriptional changes associated with the lifespan extension and uncovered pathways that may be associated with the age-dependent decline of biological functions.

Indexed as

Gene Expression RegulationTranscriptomeAnimalsCircadian RhythmDrosophilaDrosophila melanogasterFemaleFertilityGene Expression ProfilingGlutamate-Cysteine LigaseGlutathioneLocomotionLongevityMaleNeuronsStress, PhysiologicalGlutamate-Cysteine LigaseGlutathioneCircadian rhythmicityDrosophila melanogasterFertilityGene expressionGlutathioneLifespanLocomotor activity

Identifiers

PMID28105938
PMCPMC5249042
OpenAlexW2564003969

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LicenceCC BY
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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.