Evidence map›Paper›PMID 30890658›Full record

ArticleScience signaling2019

HIPK2 is necessary for type I interferon-mediated antiviral immunity.

Lili Cao, Guang Yang, Shandian Gao, Chunxia Jing, Ruth R Montgomery, Yuxin Yin, Penghua Wang, Erol Fikrig, Fuping You

Open access · greenAbstract read
In one paragraph

Article in Science signaling, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  7. Small Molecule Allosteric Inhibitor of HIPK2 as a Novel Therapy against Kidney Fibrosis.Journal of the American Society of Nephrology : JASN · 2024
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  13. HIPK2 phosphorylates HDAC3 for NF-κB acetylation to ameliorate colitis-associated colorectal carcinoma and sepsis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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  18. The nutrient sensor OGT regulates Hipk stability and tumorigenic-like activities inProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Lili CaoInstitute of Systems Biomedicine, Department of Immunology, School of Basic Medical Sciences, Beijing Key Laboratory of Tumor Systems Biology, Peking University Health Science Center, Beijing 100191, China.ORCID 0000-0003-4608-0723
Guang YangSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 208022, USA.ORCID 0000-0003-1688-515X
Shandian GaoSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 208022, USA.
Chunxia JingDepartment of Epidemiology, School of Medicine, Jinan University, Guangzhou 510632, China.ORCID 0000-0001-7333-4181
Ruth R MontgomerySection of Rheumatology, Yale University School of Medicine, New Haven, CT 06510, USA.ORCID 0000-0002-8661-4454
Yuxin YinInstitute of Systems Biomedicine, Department of Immunology, School of Basic Medical Sciences, Beijing Key Laboratory of Tumor Systems Biology, Peking University Health Science Center, Beijing 100191, China.
Penghua WangSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 208022, USA.
Erol FikrigSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 208022, USA. fupingyou@hsc.pku.edu.cn erol.fikrig@yale.edu.ORCID 0000-0002-5884-6047
Fuping YouInstitute of Systems Biomedicine, Department of Immunology, School of Basic Medical Sciences, Beijing Key Laboratory of Tumor Systems Biology, Peking University Health Science Center, Beijing 100191, China. fupingyou@hsc.pku.edu.cn erol.fikrig@yale.edu.ORCID 0000-0002-7444-729X
Peking University · CNYale University · USJinan University · CNHoward Hughes Medical Institute · US

Funding

Systems investigation of vaccine responses in B cell depleted autoimmune patientsU19AI089992 · NIAID · YALE UNIVERSITY · PI David A. Hafler, RUTH R MONTGOMERY · 2010 to 2026
$50.4M
The role of NLRP6 and DHX15 in control of infection by RNA virusesR01AI127865 · NIAID · YALE UNIVERSITY · PI FIKRIG, EROL, FLAVELL, RICHARD A · 2018 to 2022
$2.1M
NIAID NIH HHS R01 AI127865NIAID NIH HHS U19 AI089992
6 · The paper itself

Abstract

Precise control of interferons (IFNs) is crucial to maintain immune homeostasis. Here, we demonstrated that homeodomain-interacting protein kinase 2 (HIPK2) was required for the production of type I IFNs in response to RNA virus infection. HIPK2 deficiency markedly impaired IFN production in macrophages after vesicular stomatitis virus (VSV) infection, and HIPK2-deficient mice were more susceptible to lethal VSV disease than were wild-type mice. After VSV infection, HIPK2 was cleaved by active caspases, which released a hyperactive, N-terminal fragment that translocated to the nucleus and further augmented antiviral responses. In part, HIPK2 interacted with ELF4 and promoted its phosphorylation at Ser

Indexed as

AnimalsCell NucleusChlorocebus aethiopsDNA-Binding ProteinsHEK293 CellsHeLa CellsHumansInterferon Type IMiceMice, KnockoutProtein Serine-Threonine KinasesTranscription FactorsVero CellsVesicular StomatitisVesiculovirusDNA-Binding ProteinsElf4 protein, mouseHipk2 protein, mouseInterferon Type IProtein Serine-Threonine KinasesTranscription Factors

Identifiers

PMID30890658
PMCPMC6893850
OpenAlexW2924817356

What OpenQuestion holds

Textmetadata
LicenceTDM
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.