Evidence map›Paper›PMID 33600488›Full record

ArticlePLoS pathogens2021

A novel role of Zebrafish TMEM33 in negative regulation of interferon production by two distinct mechanisms.

Long-Feng Lu, Can Zhang, Zhuo-Cong Li, Xiao-Yu Zhou, Jing-Yu Jiang, Dan-Dan Chen, Yong-An Zhang, Feng Xiong, Fang Zhou, Shun Li

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. TMEM33 deletion potentiates anti-tumor CD8bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. ZebrafishJournal of virology · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Two DuplicatedFrontiers in immunology · 2021
    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

10 authors at 2 institutions in 1 country.

Long-Feng LuInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
Can ZhangInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
Zhuo-Cong LiInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
Xiao-Yu ZhouInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
Jing-Yu JiangInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
Dan-Dan ChenInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
Yong-An ZhangInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.ORCID 0000-0002-9956-3879
Feng XiongInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
Fang ZhouInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
Shun LiInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.ORCID 0000-0002-3629-9900
Chinese Academy of Sciences · CNDalian Ocean University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transmembrane protein 33 (TMEM33) was originally identified as an endoplasmic reticulum (ER) protein that influences the tubular structure of the ER and modulates intracellular calcium homeostasis. However, the role of TMEM33 in antiviral immunity in vertebrates has not been elucidated. In this article, we demonstrate that zebrafish TMEM33 is a negative regulator of virus-triggered interferon (IFN) induction via two mechanisms: mitochondrial antiviral signaling protein (MAVS) ubiquitination and a decrease in the kinase activity of TANK binding kinase 1 (TBK1). Upon stimulation with viral components, tmem33 was remarkably upregulated in the zebrafish liver cell line. The IFNφ1 promoter (IFNφ1pro) activity and mRNA level induced by retinoic acid-inducible gene (RIG)-I-like receptors (RLRs) were significantly inhibited by TMEM33. Knockdown of TMEM33 increased host ifn transcription. Subsequently, we found that TMEM33 was colocalized in the ER and interacted with the RLR cascades, whereas MAVS was degraded by TMEM33 during the K48-linked ubiquitination. On the other hand, TMEM33 reduced the phosphorylation of mediator of IFN regulatory factor 3 (IRF3) activation (MITA)/IRF3 by acting as a decoy substrate of TBK1, which was also phosphorylated. A functional domain assay revealed that the N-terminal transmembrane domain 1 (TM1) and TM2 regions of TMEM33 were necessary for IFN suppression. Finally, TMEM33 significantly attenuated the host cellular antiviral capacity by blocking the IFN response. Taken together, our findings provide insight into the different mechanisms employed by TMEM33 in cellular IFN-mediated antiviral process.

Indexed as

Gene Expression RegulationAnimalsInterferonsLiverMembrane ProteinsPhosphorylationRhabdoviridaeRhabdoviridae InfectionsUbiquitinationZebrafishZebrafish ProteinsInterferonsMembrane ProteinsZebrafish Proteins

Identifiers

PMID33600488
PMCPMC7891750
OpenAlexW3133039085

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.