Evidence map›Paper›PMID 34440743›Full record

ArticleCells2021

UBE2L3, a Partner of MuRF1/TRIM63, Is Involved in the Degradation of Myofibrillar Actin and Myosin.

Dulce Peris-Moreno, Mélodie Malige, Agnès Claustre, Andrea Armani, Cécile Coudy-Gandilhon, Christiane Deval, Daniel Béchet, Pierre Fafournoux, Marco Sandri, Lydie Combaret and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.2field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

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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

12 authors at 2 institutions in 2 countries.

Dulce Peris-MorenoUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.ORCID 0000-0001-6818-5900
Mélodie MaligeUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.
Agnès ClaustreUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.
Andrea ArmaniDepartment of Biomedical Sciences, Venetian Institute of Molecular Medicine, University of Padua, 35100 Padova, Italy.
Cécile Coudy-GandilhonUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.
Christiane DevalUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.
Daniel BéchetUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.ORCID 0000-0002-3812-8099
Pierre FafournouxUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.ORCID 0000-0002-4900-4331
Marco SandriDepartment of Biomedical Sciences, Venetian Institute of Molecular Medicine, University of Padua, 35100 Padova, Italy.
Lydie CombaretUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.ORCID 0000-0001-6550-8700
Daniel TaillandierUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.
Cécile PolgeUniversité Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.ORCID 0000-0002-8730-5776
Université Clermont Auvergne · FRUniversity of Padua · IT

Funding

Association Française contre les Myopathies #19521European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 813599Fondation pour la Recherche Médicale DEQ20180339180French government IDEX-ISITE initiative CAP 20e25 16-IDEX-0001
6 · The paper itself

Abstract

The ubiquitin proteasome system (UPS) is the main player of skeletal muscle wasting, a common characteristic of many diseases (cancer, etc.) that negatively impacts treatment and life prognosis. Within the UPS, the E3 ligase MuRF1/TRIM63 targets for degradation several myofibrillar proteins, including the main contractile proteins alpha-actin and myosin heavy chain (MHC). We previously identified five E2 ubiquitin-conjugating enzymes interacting with MuRF1, including UBE2L3/UbcH7, that exhibited a high affinity for MuRF1 (K

Indexed as

ActinsAnimalsCell LineDexamethasoneHistocompatibility Antigens Class IIMaleMiceMice, Inbred C57BLMuscle Fibers, SkeletalMuscle ProteinsMuscular AtrophyProtein BindingRNA InterferenceRNA, Small InterferingTripartite Motif ProteinsUbiquitin-Conjugating EnzymesActinsDexamethasoneHistocompatibility Antigens Class IIMuscle ProteinsRNA, Small InterferingTrim63 protein, mouseTripartite Motif ProteinsUbe2l3 protein, mouseUbiquitin-Conjugating EnzymesUbiquitin-Protein Ligasesalpha-actincontractile proteinsglucocorticoidsMicroScale-ThermophoresisMuRF1/TRIM63myosinskeletal muscle atrophyUBE2L3/UbcH7ubiquitinating enzymes

Identifiers

PMID34440743
PMCPMC8392593
OpenAlexW3192888142

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.