Evidence map›Paper›PMID 35347428›Full record

ArticleCellular and molecular life sciences : CMLS2022

Selective cleavage of ncRNA and antiviral activity by RNase2/EDN in THP1-induced macrophages.

Lu Lu, Jiarui Li, Ranlei Wei, Irene Guidi, Luca Cozzuto, Julia Ponomarenko, Guillem Prats-Ejarque, Ester Boix

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. cP-RNA-seq for tRNA half sequencing.Methods in enzymology · 2025
    Article
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  11. Article
  12. Article
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  14. Article
  15. 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

8 authors at 3 institutions in 2 countries.

Lu Lu *Department of Biochemistry and Molecular Biology, Faculty of Biosciences, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain. lu.lu@sicau.edu.cn.
Jiarui Li *Department of Biochemistry and Molecular Biology, Faculty of Biosciences, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain.
Ranlei WeiNational Frontier Center of Disease Molecular Network, West China Hospital, Sichuan University, Chengdu, 610041, China.
Irene GuidiDepartment of Biochemistry and Molecular Biology, Faculty of Biosciences, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain.
Luca CozzutoBioinformatic Unit, Centre de Regulació Genòmica (CRG), Barcelona, Spain.
Julia PonomarenkoBioinformatic Unit, Centre de Regulació Genòmica (CRG), Barcelona, Spain.
Guillem Prats-EjarqueDepartment of Biochemistry and Molecular Biology, Faculty of Biosciences, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain.
Ester BoixDepartment of Biochemistry and Molecular Biology, Faculty of Biosciences, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain. Ester.Boix@uab.es.ORCID http://orcid.org/0000-0003-1790-2142
Universitat Autònoma de Barcelona · ESCentre for Genomic Regulation · ESSichuan University · CN

Funding

Ministerio de Economía y Competitividad PID2019-106123GB-I00
6 · The paper itself

Abstract

RNase2 is the member of the RNaseA family most abundant in macrophages. Here, we knocked out RNase2 in THP-1 cells and analysed the response to Respiratory Syncytial Virus (RSV). RSV induced RNase2 expression, which significantly enhanced cell survival. Next, by cP-RNAseq sequencing, which amplifies the cyclic-phosphate endonuclease products, we analysed the ncRNA population. Among the ncRNAs accumulated in WT vs KO cells, we found mostly tRNA-derived fragments (tRFs) and second miRNAs. Differential sequence coverage identified tRFs from only few parental tRNAs, revealing a predominant cleavage at anticodon and D-loops at U/C (B1) and A (B2) sites. Selective tRNA cleavage was confirmed in vitro using the recombinant protein. Likewise, only few miRNAs were significantly more abundant in WT vs RNase2-KO cells. Complementarily, by screening of a tRF & tiRNA array, we identified an enriched population associated to RNase2 expression and RSV exposure. The results confirm the protein antiviral action and provide the first evidence of its cleavage selectivity on ncRNAs.

Indexed as

Antiviral AgentsRNA, UntranslatedAnticodonMacrophagesRNA, TransferAnticodonAntiviral AgentsRNA, TransferRNA, UntranslatedmiRNARNaseRSVtRFtRNAVirus

Identifiers

PMID35347428
PMCPMC8960563
OpenAlexW4220802209

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.