Evidence map›Paper›PMID 35013429›Full record

ArticleScientific reports2022

Systematic identification of NF90 target RNAs by iCLIP analysis.

Valeria Lodde, Matteo Floris, Rachel Munk, Jennifer L Martindale, Davide Piredda, Catello Mario Panu Napodano, Francesco Cucca, Sergio Uzzau, Kotb Abdelmohsen, Myriam Gorospe and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 12 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 7 institutions in 3 countries.

Valeria LoddeDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Matteo FlorisDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Rachel MunkLaboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD, 21224, USA.
Jennifer L MartindaleLaboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD, 21224, USA.
Davide PireddaIntensive Care Unit, Emergency Department, AOU Sassari, Sassari, Italy.
Catello Mario Panu NapodanoInternal Medicine Unit, ATS Sardegna, Ospedale Civile Alghero, Sassari, Italy.
Francesco CuccaDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Sergio UzzauDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Kotb AbdelmohsenLaboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD, 21224, USA.
Myriam GorospeLaboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD, 21224, USA.
Ji Heon NohLaboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD, 21224, USA.
M Laura IddaLaboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD, 21224, USA. marialaura.idda@irgb.cnr.it.
National Institute on Aging · USUniversity of Sassari · ITInstitute of Genetic and Biomedical Research · ITATS Sardegna (Italy) · ITAzienda Ospedaliero Universitaria di Sassari · ITInstitute on Aging · USNational Institutes of Health · US

Funding

Post-transcriptional Regulation Of Proliferative and Stress Response GenesZIAAG000511 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$25.4M
6 · The paper itself

Abstract

RNA-binding proteins (RBPs) interact with and determine the fate of many cellular RNAs directing numerous essential roles in cellular physiology. Nuclear Factor 90 (NF90) is an RBP encoded by the interleukin enhancer-binding factor 3 (ILF3) gene that has been found to influence RNA metabolism at several levels, including pre-RNA splicing, mRNA turnover, and translation. To systematically identify the RNAs that interact with NF90, we carried out iCLIP (individual-nucleotide resolution UV crosslinking and immunoprecipitation) analysis in the human embryonic fibroblast cell line HEK-293. Interestingly, many of the identified RNAs encoded proteins involved in the response to viral infection and RNA metabolism. We validated a subset of targets and investigated the impact of NF90 on their expression levels. Two of the top targets, IRF3 and IRF9 mRNAs, encode the proteins IRF3 and IRF9, crucial regulators of the interferon pathway involved in the SARS-CoV-2 immune response. Our results support a role for NF90 in modulating key genes implicated in the immune response and offer insight into the immunological response to the SARS-CoV-2 infection.

Indexed as

Cells, CulturedCOVID-19HEK293 CellsHumansImmunoprecipitationInterferon Regulatory Factor-3Interferon-Stimulated Gene Factor 3, gamma SubunitNuclear Factor 90 ProteinsProtein BindingRNARNA-Binding ProteinsRNA InterferenceRNA, MessengerRNA-SeqRNA StabilitySARS-CoV-2Interferon Regulatory Factor-3Interferon-Stimulated Gene Factor 3, gamma SubunitIRF3 protein, humanIRF9 protein, humanNuclear Factor 90 ProteinsRNARNA-Binding ProteinsRNA, Messenger

Identifiers

PMID35013429
PMCPMC8748789
OpenAlexW4206248637

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.