Evidence map›Paper›PMID 32090465›Full record

ArticleEMBO reports2020

Proteasome mapping reveals sexual dimorphism in tissue-specific sensitivity to protein aggregations.

Edmund Charles Jenkins, Nagma Shah, Maria Gomez, Gabriella Casalena, Dazhi Zhao, Timothy C Kenny, Sara Rose Guariglia, Giovanni Manfredi, Doris Germain

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 41 citations in OpenAlex.

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  9. Review
  10. Sex, senescence, senolytics, and cognition.Frontiers in aging neuroscience · 2025
    Review
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  12. Review
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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

9 authors at 3 institutions in 1 country.

Edmund Charles JenkinsDivision of Hematology/Oncology, Department of Medicine, Icahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY, USA.
Nagma ShahDivision of Hematology/Oncology, Department of Medicine, Icahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY, USA.
Maria GomezDivision of Hematology/Oncology, Department of Medicine, Icahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY, USA.
Gabriella CasalenaFeil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, NY, USA.
Dazhi ZhaoFeil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, NY, USA.
Timothy C KennyDivision of Hematology/Oncology, Department of Medicine, Icahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY, USA.
Sara Rose GuarigliaCity University of New York, College of Staten Island, Staten Island, NY, USA.
Giovanni ManfrediFeil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, NY, USA.ORCID 0000-0003-3893-1348
Doris GermainDivision of Hematology/Oncology, Department of Medicine, Icahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY, USA.ORCID 0000-0001-6597-0196
Icahn School of Medicine at Mount Sinai · USCornell University · USCollege of Staten Island · US

Funding

TRAINING PROGRAM IN CANCER THERAPYT32CA078207 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI James J Manfredi · 1999 to 2026
$11.6M
Mitochondria quality control in SOD1-ALSR01NS062055 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI MANFREDI, GIOVANNI · 2009 to 2019
$3.7M
Mitochondrial inter membrane space-IMS unfolded protein response in familial ALSR01NS084486 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GERMAIN, DORIS A, MANFREDI, GIOVANNI · 2014 to 2018
$1.9M
NCI NIH HHS T32 CA078207NINDS NIH HHS R01 NS062055NINDS NIH HHS R01 NS084486
6 · The paper itself

Abstract

Defects in the proteasome can result in pathological proteinopathies. However, the pathogenic role of sex- and tissue-specific sensitivity to proteotoxic stress remains elusive. Here, we map the proteasome activity across nine tissues, in male and female mice, and demonstrate strong sexual dimorphism in proteasome activity, where females have significantly higher activity in several tissues. Further, we report drastic differences in proteasome activity among tissues, independently of proteasome concentration, which are exacerbated under stress conditions. Sexual dimorphism in proteasome activity is confirmed in a SOD1 ALS mouse model, in which the spinal cord, a tissue with comparatively low proteasome activity, is severely affected. Our results offer mechanistic insight into tissue-specific sensitivities to proteostasis stress and into sex differences in the progression of neurodegenerative proteinopathies.

Indexed as

Amyotrophic Lateral SclerosisSex CharacteristicsAnimalsDisease Models, AnimalFemaleMaleMiceMice, TransgenicProteasome Endopeptidase ComplexProtein AggregatesSuperoxide DismutaseSuperoxide Dismutase-1Proteasome Endopeptidase ComplexProtein AggregatesSuperoxide DismutaseSuperoxide Dismutase-1amyotrophic lateral sclerosisgender differencesproteasomeprotein aggregatesubiquitin

Identifiers

PMID32090465
PMCPMC7132179
OpenAlexW3008720880

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.