Evidence map›Paper›PMID 31433824›Full record

ArticlePLoS pathogens2019

The heterogeneous nuclear ribonucleoprotein hnRNPM inhibits RNA virus-triggered innate immunity by antagonizing RNA sensing of RIG-I-like receptors.

Pan Cao, Wei-Wei Luo, Chen Li, Zhen Tong, Zhou-Qin Zheng, Lu Zhou, Yong Xiong, Shu Li

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

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  19. Toll-Like Receptors as a Therapeutic Target in the Era of Immunotherapies.Frontiers in cell and developmental biology · 2021
    Review
  20. Article
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 2 institutions in 1 country.

Pan CaoDepartment of Infectious Diseases, Zhongnan Hospital of Wuhan University, College of Life Sciences, Medical Research Institute, Wuhan University, Wuhan, China.
Wei-Wei LuoWuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.ORCID 0000-0002-8541-4274
Chen LiDepartment of Infectious Diseases, Zhongnan Hospital of Wuhan University, College of Life Sciences, Medical Research Institute, Wuhan University, Wuhan, China.ORCID 0000-0002-0547-6820
Zhen TongWuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Zhou-Qin ZhengWuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.ORCID 0000-0003-2745-5841
Lu ZhouDepartment of Infectious Diseases, Zhongnan Hospital of Wuhan University, College of Life Sciences, Medical Research Institute, Wuhan University, Wuhan, China.
Yong XiongDepartment of Infectious Diseases, Zhongnan Hospital of Wuhan University, College of Life Sciences, Medical Research Institute, Wuhan University, Wuhan, China.ORCID 0000-0003-0678-4064
Shu LiDepartment of Infectious Diseases, Zhongnan Hospital of Wuhan University, College of Life Sciences, Medical Research Institute, Wuhan University, Wuhan, China.ORCID 0000-0002-0007-5198
Wuhan University · CNChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recognition of viral RNA by the retinoic acid-inducible gene-I (RIG-I)-like receptors (RLRs), including RIG-I and MDA5, initiates innate antiviral responses. Although regulation of RLR-mediated signal transduction has been extensively investigated, how the recognition of viral RNA by RLRs is regulated remains enigmatic. In this study, we identified heterogeneous nuclear ribonucleoprotein M (hnRNPM) as a negative regulator of RLR-mediated signaling. Overexpression of hnRNPM markedly inhibited RNA virus-triggered innate immune responses. Conversely, hnRNPM-deficiency increased viral RNA-triggered innate immune responses and inhibited replication of RNA viruses. Viral infection caused translocation of hnRNPM from the nucleus to the cytoplasm. hnRNPM interacted with RIG-I and MDA5, and impaired the binding of the RLRs to viral RNA, leading to inhibition of innate antiviral response. Our findings suggest that hnRNPM acts as an important decoy for excessive innate antiviral immune response.

Indexed as

DEAD Box Protein 58HEK293 CellsHeLa CellsHeterogeneous-Nuclear Ribonucleoprotein Group MHumansProtein BindingRNA, ViralRNA VirusesRNA Virus InfectionsSignal TransductionVirus ReplicationDEAD Box Protein 58Heterogeneous-Nuclear Ribonucleoprotein Group MRNA, Viral

Identifiers

PMID31433824
PMCPMC6703689
OpenAlexW2969489218

What OpenQuestion holds

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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.