Evidence map›Paper›PMID 35277432›Full record

ArticleGenome research2022

Genome-wide transcript and protein analysis highlights the role of protein homeostasis in the aging mouse heart.

Isabela Gerdes Gyuricza, Joel M Chick, Gregory R Keele, Andrew G Deighan, Steven C Munger, Ron Korstanje, Steven P Gygi, Gary A Churchill

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed, 36 citations in OpenAlex.

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  8. Fifteen years of the Diversity Outbred mouse model: a review.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
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  18. Transcriptional drift in aging cells: A global decontroller.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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

8 authors at 3 institutions in 1 country.

Isabela Gerdes GyuriczaThe Jackson Laboratory, Bar Harbor, Maine 04609, USA.ORCID 0000-0002-7969-1910
Joel M ChickVividion Therapeutics, San Diego, California 92121, USA.
Gregory R KeeleThe Jackson Laboratory, Bar Harbor, Maine 04609, USA.
Andrew G DeighanThe Jackson Laboratory, Bar Harbor, Maine 04609, USA.
Steven C MungerThe Jackson Laboratory, Bar Harbor, Maine 04609, USA.
Ron KorstanjeThe Jackson Laboratory, Bar Harbor, Maine 04609, USA.
Steven P GygiHarvard Medical School, Boston, Massachusetts 02115, USA.
Gary A ChurchillThe Jackson Laboratory, Bar Harbor, Maine 04609, USA.
Jackson Laboratory · USHarvard University · USVividion Therapeutics (United States) · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Translational CoreP30AG038070 · NIA · JACKSON LABORATORY · PI Gary A Churchill · 2010 to 2026
$19.3M
Leveraging Natural Genetic Diversity and Systems Genetics to Elucidate the Complex Hierarchy of Gene Regulation Underlying Ground State Pluripotency, Cell Fate Decisions and Tissue HomeostasisR35GM133495 · NIGMS · JACKSON LABORATORY · PI MUNGER, STEVEN CARMEN · 2019 to 2023
$2.0M
Bayesian Modeling of Mass-Spec Proteomics Data to Advance Studies of the Genetic Regulation of ProteinsF32GM134599 · NIGMS · JACKSON LABORATORY · PI KEELE, GREGORY R · 2020 to 2021
$139k
NCI NIH HHS P30 CA034196NIA NIH HHS P30 AG038070NIGMS NIH HHS F32 GM134550NIGMS NIH HHS F32 GM134599NIGMS NIH HHS R35 GM133495
6 · The paper itself

Abstract

Investigation of the molecular mechanisms of aging in the human heart is challenging because of confounding factors, such as diet and medications, as well as limited access to tissues from healthy aging individuals. The laboratory mouse provides an ideal model to study aging in healthy individuals in a controlled environment. However, previous mouse studies have examined only a narrow range of the genetic variation that shapes individual differences during aging. Here, we analyze transcriptome and proteome data from 185 genetically diverse male and female mice at ages 6, 12, and 18 mo to characterize molecular changes that occur in the aging heart. Transcripts and proteins reveal activation of pathways related to exocytosis and cellular transport with age, whereas processes involved in protein folding decrease with age. Additional changes are apparent only in the protein data including reduced fatty acid oxidation and increased autophagy. For proteins that form complexes, we see a decline in correlation between their component subunits with age, suggesting age-related loss of stoichiometry. The most affected complexes are themselves involved in protein homeostasis, which potentially contributes to a cycle of progressive breakdown in protein quality control with age. Our findings highlight the important role of post-transcriptional regulation in aging. In addition, we identify genetic loci that modulate age-related changes in protein homeostasis, suggesting that genetic variation can alter the molecular aging process.

Indexed as

AgingProteostasisAnimalsAutophagyFemaleGene Expression RegulationMaleMiceTranscriptome

Identifiers

PMID35277432
PMCPMC9104701
OpenAlexW4220957049

What OpenQuestion holds

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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.