Evidence map›Paper›PMID 30649422›Full record

ArticleNucleic acids research2019

Single cell analysis reveals the involvement of the long non-coding RNA Pvt1 in the modulation of muscle atrophy and mitochondrial network.

Enrico Alessio, Lisa Buson, Francesco Chemello, Caterina Peggion, Francesca Grespi, Paolo Martini, Maria L Massimino, Beniamina Pacchioni, Caterina Millino, Chiara Romualdi and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 4% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 83 citations in OpenAlex.

  1. Pooled it
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  10. Epigenetics of Skeletal Muscle Atrophy.International journal of molecular sciences · 2024
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  14. Mitochondrial dysfunction: roles in skeletal muscle atrophy.Journal of translational medicine · 2023
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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

14 authors at 2 institutions in 1 country.

Enrico AlessioDepartment of Biology, University of Padova, 35131 Padova, Italy.
Lisa BusonDepartment of Biology, University of Padova, 35131 Padova, Italy.
Francesco ChemelloDepartment of Biology, University of Padova, 35131 Padova, Italy.
Caterina PeggionDepartment of Biomedical Sciences, University of Padova, 35131 Padova, Italy.
Francesca GrespiDepartment of Biology, University of Padova, 35131 Padova, Italy.
Paolo MartiniDepartment of Biology, University of Padova, 35131 Padova, Italy.
Maria L MassiminoCNR Neuroscience Institute, 35131 Padova, Italy.
Beniamina PacchioniDepartment of Biology, University of Padova, 35131 Padova, Italy.
Caterina MillinoDepartment of Biology, University of Padova, 35131 Padova, Italy.
Chiara RomualdiDepartment of Biology, University of Padova, 35131 Padova, Italy.
Alessandro BertoliDepartment of Biomedical Sciences, University of Padova, 35131 Padova, Italy.
Luca ScorranoDepartment of Biology, University of Padova, 35131 Padova, Italy.
Gerolamo LanfranchiDepartment of Biology, University of Padova, 35131 Padova, Italy.
Stefano CagninDepartment of Biology, University of Padova, 35131 Padova, Italy.
University of Padua · ITNeuroscience Institute · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) are emerging as important players in the regulation of several aspects of cellular biology. For a better comprehension of their function, it is fundamental to determine their tissue or cell specificity and to identify their subcellular localization. In fact, the activity of lncRNAs may vary according to cell and tissue specificity and subcellular compartmentalization. Myofibers are the smallest complete contractile system of skeletal muscle influencing its contraction velocity and metabolism. How lncRNAs are expressed in different myofibers, participate in metabolism regulation and muscle atrophy or how they are compartmentalized within a single myofiber is still unknown. We compiled a comprehensive catalog of lncRNAs expressed in skeletal muscle, associating the fiber-type specificity and subcellular location to each of them, and demonstrating that many lncRNAs can be involved in the biological processes de-regulated during muscle atrophy. We demonstrated that the lncRNA Pvt1, activated early during muscle atrophy, impacts mitochondrial respiration and morphology and affects mito/autophagy, apoptosis and myofiber size in vivo. This work corroborates the importance of lncRNAs in the regulation of metabolism and neuromuscular pathologies and offers a valuable resource to study the metabolism in single cells characterized by pronounced plasticity.

Indexed as

AnimalsApoptosisCell CompartmentationFemaleGene Expression ProfilingGenome, HumanHumansIn Situ Hybridization, FluorescenceMiceMitochondriaMitophagyMuscle ContractionMuscle, SkeletalMuscular AtrophyRNA, Long NoncodingSingle-Cell AnalysisPVT1 long-non-coding RNA, humanRNA, Long Noncoding

Identifiers

PMID30649422
PMCPMC6393313
OpenAlexW2910043676

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.