Evidence map›Paper›PMID 25465735›Full record

ArticleNeurobiology of aging2015

Accelerated protein damage in brains of PIMT+/- mice; a possible model for the variability of cognitive decline in human aging.

Zhenxia Qin, Aleksandra Dimitrijevic, Dana W Aswad

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of aging, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 36 citations in OpenAlex.

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  6. Genesis and regulation of C-terminal cyclic imides from protein damage.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  19. Identification of long-lived synaptic proteins by proteomic analysis of synaptosome protein turnover.Proceedings of the National Academy of Sciences of the United States of America · 2018
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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

3 authors at 1 institution in 1 country.

Zhenxia QinDepartment of Molecular Biology & Biochemistry, University of California, Irvine, Irvine, CA, USA.
Aleksandra DimitrijevicDepartment of Molecular Biology & Biochemistry, University of California, Irvine, Irvine, CA, USA.
Dana W AswadDepartment of Molecular Biology & Biochemistry, University of California, Irvine, Irvine, CA, USA. Electronic address: dwaswad@uci.edu.
University of California, Irvine · US

Funding

Protein Methylation in BrainR01NS017269 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI ASWAD, DANA WILLIAM · 1985 to 2012
$2.4M
NINDS NIH HHS NS17269NINDS NIH HHS R01 NS017269
6 · The paper itself

Abstract

Isoaspartate formation is a common type of protein damage normally kept in check by the repair enzyme protein-L-isoaspartyl methyltransferase (PIMT). Mice with a knockout of the gene (Pcmt1) for this enzyme (KO, -/-) exhibit a pronounced neuropathology with fatal epileptic seizures at 30-60 days. Heterozygous (HZ, +/-) mice have 50% of the PIMT activity found in wild-type (WT, +/+) mice, but appear normal. To see if HZ mice exhibit accelerated aging at the molecular level, we compared brain extracts from HZ and WT mice at 8 months and 2 years with regard to PIMT activity, isoaspartate levels, and activity of an endogenous PIMT substrate, creatine kinase B. PIMT activity declined modestly with age in both genotypes. Isoaspartate was significantly higher in HZ than WT mice at 8 months and more so at 2 years, rising 5× faster in HZ males and 3× faster in females. Creatine kinase activity decreased with age and was always lower in the HZ mice. These findings suggest the individual variation of human PIMT levels may significantly influence the course of age-related central nervous system dysfunction.

Indexed as

AgingAnimalsBrainCognition DisordersCreatine Kinase, BB FormDisease Models, AnimalFemaleHumansIsoaspartic AcidMaleMice, Inbred C57BLMice, KnockoutNerve Tissue ProteinsProtein D-Aspartate-L-Isoaspartate MethyltransferaseCreatine Kinase, BB FormIsoaspartic AcidNerve Tissue ProteinsPCMT1 protein, humanProtein D-Aspartate-L-Isoaspartate MethyltransferaseCreatine kinaseDeamidationIsoaspartateMethyltransferaseProtein damageProtein repair

Identifiers

PMID25465735
PMCPMC4315693
OpenAlexW2007903221

What OpenQuestion holds

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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.