Evidence map›Paper›PMID 37255478›Full record

ArticleJournal of virology2023

DTX3L Enhances Type I Interferon Antiviral Response by Promoting the Ubiquitination and Phosphorylation of TBK1.

Jiaqi Huang, Zhengrong Chen, Yunfei Ye, Yu Shao, Peijie Zhu, Xiaoping Li, Yu Ma, Fei Xu, Ji Zhou, Mengyun Wu and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 22 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

14 authors at 1 institution in 1 country.

Jiaqi Huang *Department of Respiratory Medicine, Children's Hospital of Soochow University, Suzhou, People's Republic of China.
Zhengrong Chen *Department of Respiratory Medicine, Children's Hospital of Soochow University, Suzhou, People's Republic of China.
Yunfei Ye *Institutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.
Yu ShaoInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.
Peijie ZhuInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.
Xiaoping LiInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.
Yu MaDepartment of Respiratory Medicine, Children's Hospital of Soochow University, Suzhou, People's Republic of China.
Fei XuInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.
Ji ZhouInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.
Mengyun WuInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.
Xiu GaoInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.
Yi YangInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.
Jinping ZhangInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, People's Republic of China.ORCID 0000-0001-5537-5131
Chuangli HaoDepartment of Respiratory Medicine, Children's Hospital of Soochow University, Suzhou, People's Republic of China.
Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies already revealed that some E3 ubiquitin ligases participated in the immune response after viral infection by regulating the type I interferon (IFN) pathway. Here, we demonstrated that type I interferon signaling enhanced the translocation of ETS1 to the nucleus and the promoter activity of E3 ubiquitin ligase DTX3L (deltex E3 ubiquitin ligase 3L) after virus infection and thus increased the expression of DTX3L. Further experiments suggested that DTX3L ubiquitinated TBK1 at K30 and K401 sites on K63-linked ubiquitination pathway. DTX3L was also necessary for mediating the phosphorylation of TBK1 through binding with the tyrosine kinase SRC: both together enhanced the activation of TBK1. Therefore, DTX3L, being an important positive-feedback regulator of type I interferon, exerted a key role in antiviral response.

Indexed as

Immunity, InnateInterferon Type IProtein Serine-Threonine KinasesRespiratory Syncytial Virus InfectionsUbiquitin-Protein LigasesPhosphorylationRespiratory Syncytial VirusesUbiquitinationInterferon Type IProtein Serine-Threonine KinasesUbiquitin-Protein Ligasesantiviral responsedeltex E3 ubiquitin ligase 3LDTX3Lrespiratory syncytial virustype I interferon

Identifiers

PMID37255478
PMCPMC10308958
OpenAlexW4378782626

What OpenQuestion holds

Textmetadata
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.