Evidence map›Paper›PMID 31341090›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Intrinsic expression of viperin regulates thermogenesis in adipose tissues.

John Eom, Jeong Jin Kim, Seul Gi Yoon, Haengdueng Jeong, Soojin Son, Jae Bong Lee, Jihye Yoo, Hyun Ju Seo, Yejin Cho, Ku Sul Kim and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed, 67 citations in OpenAlex.

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  15. Article
  16. Viperin is anti-viralThe Journal of general virology · 2021
    Article
  17. Article
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  19. Article
  20. Viperin Reveals Its True Function.Annual review of virology · 2020
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

John EomSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.
Jeong Jin KimSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.
Seul Gi YoonKorea Mouse Phenotyping Center, Seoul National University, 08826 Seoul, Republic of Korea.
Haengdueng JeongSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.
Soojin SonKorea Mouse Phenotyping Center, Seoul National University, 08826 Seoul, Republic of Korea.
Jae Bong LeeSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.
Jihye YooSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.
Hyun Ju SeoKorea Mouse Phenotyping Center, Seoul National University, 08826 Seoul, Republic of Korea.
Yejin ChoSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.
Ku Sul KimSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.
Kyung Mi ChoiSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.
Il Yong KimKorea Mouse Phenotyping Center, Seoul National University, 08826 Seoul, Republic of Korea.
Hui-Young LeeDepartment of Molecular Medicine, School of Medicine, Gachon University, 21999 Incheon, Republic of Korea.
Ki Taek NamSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.
Peter CresswellDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06520; peter.cresswell@yale.edu snumouse@snu.ac.kr jyseo0724@yuhs.ac.
Je Kyung SeongKorea Mouse Phenotyping Center, Seoul National University, 08826 Seoul, Republic of Korea; peter.cresswell@yale.edu snumouse@snu.ac.kr jyseo0724@yuhs.ac.
Jun-Young SeoSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea; peter.cresswell@yale.edu snumouse@snu.ac.kr jyseo0724@yuhs.ac.ORCID 0000-0003-4004-2013
Yonsei University · KRSeoul National University · KRGachon University · KRYale University · US

Funding

Molecular Aspects of Human CD1d FunctionsR01AI059167 · NIAID · YALE UNIVERSITY · PI CRESSWELL, PETER · 2004 to 2019
$5.6M
Quality Control of MHC Class I Restricted Antigen ProcessingR01AI097206 · NIAID · YALE UNIVERSITY · PI CRESSWELL, PETER · 2012 to 2020
$4.1M
NIAID NIH HHS R01 AI059167NIAID NIH HHS R01 AI097206
6 · The paper itself

Abstract

Viperin is an interferon (IFN)-inducible multifunctional protein. Recent evidence from high-throughput analyses indicates that most IFN-inducible proteins, including viperin, are intrinsically expressed in specific tissues; however, the respective intrinsic functions are unknown. Here we show that the intrinsic expression of viperin regulates adipose tissue thermogenesis, which is known to counter metabolic disease and contribute to the febrile response to pathogen invasion. Viperin knockout mice exhibit increased heat production, resulting in a reduction of fat mass, improvement of high-fat diet (HFD)-induced glucose tolerance, and enhancement of cold tolerance. These thermogenic phenotypes are attributed to an adipocyte-autonomous mechanism that regulates fatty acid β-oxidation. Under an HFD, viperin expression is increased, and its function is enhanced. Our findings reveal the intrinsic function of viperin as a novel mechanism regulating thermogenesis in adipose tissues, suggesting that viperin represents a molecular target for thermoregulation in clinical contexts.

Indexed as

Gene Expression RegulationAdipocytesAdipose TissueAnimalsEnergy MetabolismMaleMiceMice, KnockoutProteinsThermogenesisViperin ProteinProteinsRsad2 protein, mouseViperin Proteinfatty acid β-oxidationinnate immunitymetabolismthermogenesisviperin

Identifiers

PMID31341090
PMCPMC6717265
OpenAlexW2963643276

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.