Evidence map›Paper›PMID 17413001›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2007

Aging perturbs 26S proteasome assembly in Drosophila melanogaster.

Vita A Vernace, Lisette Arnaud, Thomas Schmidt-Glenewinkel, Maria E Figueiredo-Pereira

Abstract readComparative Study
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
–field-weighted citation impact
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

87 citing papers in PubMed.

  1. Proteostasis and ageing dissidence.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
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  16. Proteostasis in T cell aging.Seminars in immunology · 2023
    Review
  17. Article
  18. Article
  19. Review
  20. Review

27 more citing papers are in PubMed but not listed here.

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

4 authors.

Vita A VernaceDepartment of Biological Sciences, Hunter College of CUNY, 695 Park Ave., New York, NY 10021, USA.
Lisette Arnaud
Thomas Schmidt-Glenewinkel
Maria E Figueiredo-Pereira

Funding

WILD TYPE &MUTANT P53 INTERACTIONS WITH HIV LTR DNAG12RR003037 · NCRR · HUNTER COLLEGE · PI DOTTIN, ROBERT P · 1985 to 2011
$27.6M
UBIQUITINATED PROTEIN DEGRADATION AND NEURODEGENERATIONS06GM060654 · NIGMS · HUNTER COLLEGE · PI LUINE, VICTORIA N · 2000 to 2011
$21.2M
SNRP AT HUNTER COLLEGEU54NS041073 · NINDS · HUNTER COLLEGE · PI FILBIN, MARIE T. · 2000 to 2010
$16.4M
Inflammation and the Ubiquitin/Proteasome Pathway in Neurodegeneration.R01AG028847 · NIA · HUNTER COLLEGE · PI FIGUEIREDO-PEREIRA, MARIA EMILIA · 2009 to 2010
$782k
NCRR NIH HHS G12 RR003037NCRR NIH HHS RR03037NIA NIH HHS R01 AG028847NIGMS NIH HHS GM60654NIGMS NIH HHS S06 GM060654NINDS NIH HHS NS41073NINDS NIH HHS U54 NS041073
6 · The paper itself

Abstract

Aging is associated with loss of quality control in protein turnover. The ubiquitin-proteasome pathway is critical to this quality control process as it degrades mutated and damaged proteins. We identified a unique aging-dependent mechanism that contributes to proteasome dysfunction in Drosophila melanogaster. Our studies are the first to show that the major proteasome form in old (43-47 days old) female and male flies is the weakly active 20S core particle, while in younger (1-32 days old) flies highly active 26S proteasomes are preponderant. Old (43-47 days) flies of both genders also exhibit a decline (approximately 50%) in ATP levels, which is relevant to 26S proteasomes, as their assembly is ATP-dependent. The steep declines in 26S proteasome and ATP levels were observed at an age (43-47 days) when the flies exhibited a marked drop in locomotor performance, attesting that these are "old age" events. Remarkably, treatment with a proteasome inhibitor increases ubiquitinated protein levels and shortens the life span of old but not young flies. In conclusion, our data reveal a previously unknown mechanism that perturbs proteasome activity in "old-age" female and male Drosophila most likely depriving them of the ability to effectively cope with proteotoxic damages caused by environmental and/or genetic factors.

Indexed as

Adenosine TriphosphateAgingAnimalsBlotting, WesternCytosolDrosophila melanogasterFemaleMaleProteasome Endopeptidase ComplexTime FactorsAdenosine TriphosphateATP dependent 26S proteaseProteasome Endopeptidase Complex

Identifiers

PMID17413001
PMCPMC3435146

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.