Evidence map›Paper›PMID 31345103›Full record

ArticleRNA biology2019

HuR interacts with lincBRN1a and lincBRN1b during neuronal stem cells differentiation.

Stephana Carelli, Toniella Giallongo, Federica Rey, Elisa Latorre, Matteo Bordoni, Serena Mazzucchelli, Maria Carlotta Gorio, Orietta Pansarasa, Alessandro Provenzani, Cristina Cereda and 1 more

Open access · hybridAbstract read
In one paragraph

Article in RNA biology, 2019. 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
1.6field-weighted citation impact, top 18% 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

28 citing papers in PubMed, 35 citations in OpenAlex.

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  12. A proinflammatory long noncoding RNA Lncenc1 regulates inflammasome activation in macrophage.American journal of physiology. Lung cellular and molecular physiology · 2023
    Article
  13. 1-L Transcription in Alzheimer's Disease.Current issues in molecular biology · 2022
    Article
  14. Emerging Roles of RNA-Binding Proteins in Neurodevelopment.Journal of developmental biology · 2022
    Review
  15. Review
  16. 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

11 authors at 3 institutions in 1 country.

Stephana CarelliLaboratory of Pharmacology, Department of Health Sciences, University of Milan , Milan , Italy.ORCID 0000-0003-4603-396X
Toniella GiallongoLaboratory of Pharmacology, Department of Health Sciences, University of Milan , Milan , Italy.
Federica ReyLaboratory of Pharmacology, Department of Health Sciences, University of Milan , Milan , Italy.
Elisa LatorreLaboratory of Pharmacology, Department of Health Sciences, University of Milan , Milan , Italy.
Matteo BordoniCenter of Genomic and post-Genomic, IRCCS Mondino Foundation , Pavia , Italy.
Serena MazzucchelliPediatric Clinical Research Center Fondazione "Romeo ed Enrica Invernizzi", University of Milan , Milan , Italy.ORCID 0000-0001-6904-8895
Maria Carlotta GorioDepartment of Biomedical and Clinical Sciencse L. Sacco, University of Milan , Milan , Italy.
Orietta PansarasaCenter of Genomic and post-Genomic, IRCCS Mondino Foundation , Pavia , Italy.
Alessandro ProvenzaniLaboratory of Genomic Screening Center for Integrative Biology, - CIBIO, University of Trento , Trento , Italy.ORCID 0000-0003-1652-3415
Cristina CeredaCenter of Genomic and post-Genomic, IRCCS Mondino Foundation , Pavia , Italy.ORCID 0000-0001-9571-0862
Anna Maria Di GiulioLaboratory of Pharmacology, Department of Health Sciences, University of Milan , Milan , Italy.
University of Milan · ITCenter for Genomic Science · ITUniversity of Trento · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LncRNAs play crucial roles in cellular processes and their regulatory effects in the adult brain and neural stem cells (NSCs) remain to be entirely characterized. We report that 10 lncRNAs (LincENC1, FABL, lincp21, HAUNT, PERIL, lincBRN1a, lincBRN1b, HOTTIP, TUG1 and FENDRR) are expressed during murine NSCs differentiation and interact with the RNA-binding protein ELAVL1/HuR. Furthermore, we characterize the function of two of the deregulated lncRNAs, lincBRN1a and lincBRN1b, during NSCs' differentiation. Their inhibition leads to the induction of differentiation, with a concomitant decrease in stemness and an increase in neuronal markers, indicating that they exert key functions in neuronal cells differentiation. Furthermore, we describe here that HuR regulates their half-life, suggesting their synergic role in the differentiation process. We also identify six human homologs (PANTR1, TUG1, HOTTIP, TP53COR, ELDRR and FENDRR) of the mentioned 10 lncRNAs and we report their deregulation during human iPSCs differentiation into neurons. In conclusion, our results strongly indicate a key synergic role for lncRNAs and HuR in neuronal stem cells fate.

Indexed as

AnimalsBiomarkersCell DifferentiationCell Self RenewalELAV-Like Protein 1Gene Expression Regulation, DevelopmentalGene SilencingHumansImmunohistochemistryMaleMiceNeural Stem CellsRNA, Long NoncodingBiomarkersElavl1 protein, mouseELAV-Like Protein 1RNA, Long NoncodingdifferentiationHuRlong-non-coding RNANeural stem cell

Identifiers

PMID31345103
PMCPMC6779397
OpenAlexW2964544320

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.