Evidence map›Paper›PMID 34582376›Full record

ArticleJCI insight2021

The small RNA mascRNA differentially regulates TLR-induced proinflammatory and antiviral responses.

Tao Sun, Chunxue Wei, Daoyong Wang, Xuxu Wang, Jiao Wang, Yuqing Hu, Xiaohua Mao

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Global deletion ofbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Review
  4. Long non-coding RNAMolecular therapy. Nucleic acids · 2025
    Review
  5. The Secret Life of NJournal of molecular biology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Structural basis of MALAT1 RNA maturation and mascRNA biogenesis.Nature structural & molecular biology · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
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

7 authors at 1 institution in 1 country.

Tao SunSchool of Life Science and Technology, Key Laboratory of Ministry of Education for Developmental Genes and Human Disease.
Chunxue WeiSchool of Life Science and Technology, Key Laboratory of Ministry of Education for Developmental Genes and Human Disease.
Daoyong WangDepartment of Biochemistry and Molecular Biology, School of Medicine.
Xuxu WangDepartment of Biochemistry and Molecular Biology, School of Medicine.
Jiao WangSchool of Life Science and Technology, Key Laboratory of Ministry of Education for Developmental Genes and Human Disease.
Yuqing HuDepartment of Biochemistry and Molecular Biology, School of Medicine.
Xiaohua MaoSchool of Life Science and Technology, Key Laboratory of Ministry of Education for Developmental Genes and Human Disease.
Ministry of Education of the People's Republic of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MALAT1-associated small cytoplasmic RNA (mascRNA) is a highly conserved transfer RNA-like (tRNA-like) noncoding RNA whose function remains largely unknown. We show here that this small RNA molecule played a role in the stringent control of TLR-mediated innate immune responses. mascRNA inhibited activation of NF-κB and mitogen-activated protein kinase (MAPK) signaling and the production of inflammatory cytokines in macrophages stimulated with LPS, a TLR4 ligand. Furthermore, exogenous mascRNA alleviated LPS-induced lung inflammation. However, mascRNA potentiated the phosphorylation of IRF3 and STAT1 and the transcription of IFN-related genes in response to the TLR3 ligand poly(I:C) both in vitro and in vivo. Mechanistically, mascRNA was found to enhance K48-linked ubiquitination and proteasomal degradation of TRAF6, thereby negatively regulating TLR-mediated MyD88-dependent proinflammatory signaling while positively regulating TRIF-dependent IFN signaling. Additionally, heterogeneous nuclear ribonucleoprotein H (hnRNP H) and hnRNP F were found to interact with mascRNA, promote its degradation, and contribute to the fine-tuning of TLR-triggered immune responses. Taken together, our data identify a dual role of mascRNA in both negative and positive regulation of innate immune responses.

Indexed as

Antiviral AgentsCytokinesHumansImmunity, InnateInflammationRNA, Long NoncodingRNA, Small CytoplasmicToll-Like Receptor 4Antiviral AgentsCytokinesMALAT1 long non-coding RNA, humanRNA, Long NoncodingRNA, Small CytoplasmicToll-Like Receptor 4CytokinesImmunologyInnate immunityNoncoding RNAs

Identifiers

PMID34582376
PMCPMC8663567
OpenAlexW3202009320

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.