Evidence map›Paper›PMID 34385328›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

STING facilitates nuclear import of herpesvirus genome during infection.

Yujin Hong, Heena Jeong, Kiwon Park, Sungwon Lee, Jae Youn Shim, Hyewon Kim, Yang Song, Seowoo Park, Hye Yoon Park, V Narry Kim and 1 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

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  6. Malignancy and viral infections in Sub-Saharan Africa: A review.Frontiers in virology (Lausanne, Switzerland) · 2023
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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

11 authors at 1 institution in 1 country.

Yujin HongSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea.ORCID 0000-0001-8385-6557
Heena JeongSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea.
Kiwon ParkSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea.
Sungwon LeeSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea.
Jae Youn ShimDepartment of Physics and Astronomy, Seoul National University, Seoul 08826, Republic of Korea.ORCID 0000-0001-7332-4696
Hyewon KimSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea.
Yang SongSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea.ORCID 0000-0002-7483-7845
Seowoo ParkSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea.
Hye Yoon ParkDepartment of Physics and Astronomy, Seoul National University, Seoul 08826, Republic of Korea.ORCID 0000-0003-4704-8178
V Narry KimSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea.
Kwangseog AhnSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea; ksahn@snu.ac.kr.ORCID 0000-0002-1015-245X
Seoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Once inside the host cell, DNA viruses must overcome the physical barrier posed by the nuclear envelope to establish a successful infection. The mechanism underlying this process remains unclear. Here, we show that the herpesvirus exploits the immune adaptor stimulator of interferon genes (STING) to facilitate nuclear import of the viral genome. Following the entry of the viral capsid into the cell, STING binds the viral capsid, mediates capsid docking to the nuclear pore complex via physical interaction, and subsequently enables accumulation of the viral genome in the nucleus. Silencing STING in human cytomegalovirus (HCMV)-susceptible cells inhibited nuclear import of the viral genome and reduced the ensuing viral gene expression. Overexpressing STING increased the host cell's susceptibility to HCMV and herpes simplex virus 1 by improving the nuclear delivery of viral DNA at the early stage of infection. These observations suggest that the proviral activity of STING is conserved and exploited by the herpesvirus family. Intriguingly, in monocytes, which act as latent reservoirs of HCMV, STING deficiency negatively regulated the establishment of HCMV latency and reactivation. Our findings identify STING as a proviral host factor regulating latency and reactivation of herpesviruses.

Indexed as

Capsid ProteinsCell LineCytomegalovirusDNA, ViralGene Expression Regulation, ViralGenome, ViralMembrane ProteinsRNA InterferenceRNA, Small InterferingSTING ProteinVirus InternalizationVirus ReplicationCapsid ProteinsDNA, ViralMembrane ProteinsRNA, Small InterferingSTING1 protein, humanSTING Proteincell susceptibilityHCMVnuclear importSTING

Identifiers

PMID34385328
PMCPMC8379909
OpenAlexW3191381303

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.