Evidence map›Paper›PMID 37628773›Full record

ReviewInternational journal of molecular sciences2023

Virus Infection and mRNA Nuclear Export.

Jiayin Guo, Yaru Zhu, Xiaoya Ma, Guijun Shang, Bo Liu, Ke Zhang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Nuclear mRNA export.Acta biochimica et biophysica Sinica · 2024
    Review
  13. Review
  14. Review
  15. Review
  16. 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

6 authors at 3 institutions in 1 country.

Jiayin GuoUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Yaru ZhuUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Xiaoya MaUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Guijun ShangShanxi Provincial Key Laboratory of Protein Structure Determination, Shanxi Academy of Advanced Research and Innovation, Taiyuan 030012, China.
Bo LiuKey Laboratory of Molecular Virology and Immunology, Chinese Academy of Sciences, Shanghai 200031, China.ORCID 0000-0002-5008-296X
Ke ZhangKey Laboratory of Molecular Virology and Immunology, Chinese Academy of Sciences, Shanghai 200031, China.ORCID 0000-0001-5365-3142
University of Chinese Academy of Sciences · CNChinese Academy of Sciences · CNShanxi Academy of Building Research · CN

Funding

Science and Technology Commission of Shanghai Municipality 21PJ1414500Science and Technology Commission of Shanghai Municipality 22PJ1414600Science and Technology Commission of Shanghai Municipality HS2021SHZX001
6 · The paper itself

Abstract

Gene expression in eukaryotes begins with transcription in the nucleus, followed by the synthesis of messenger RNA (mRNA), which is then exported to the cytoplasm for its translation into proteins. Along with transcription and translation, mRNA export through the nuclear pore complex (NPC) is an essential regulatory step in eukaryotic gene expression. Multiple factors regulate mRNA export and hence gene expression. Interestingly, proteins from certain types of viruses interact with these factors in infected cells, and such an interaction interferes with the mRNA export of the host cell in favor of viral RNA export. Thus, these viruses hijack the host mRNA nuclear export mechanism, leading to a reduction in host gene expression and the downregulation of immune/antiviral responses. On the other hand, the viral mRNAs successfully evade the host surveillance system and are efficiently exported from the nucleus to the cytoplasm for translation, which enables the continuation of the virus life cycle. Here, we present this review to summarize the mechanisms by which viruses suppress host mRNA nuclear export during infection, as well as the key strategies that viruses use to facilitate their mRNA nuclear export. These studies have revealed new potential antivirals that may be used to inhibit viral mRNA transport and enhance host mRNA nuclear export, thereby promoting host gene expression and immune responses.

Indexed as

Virus DiseasesActive Transport, Cell NucleusAntiviral AgentsEukaryotaHumansRNA, MessengerRNA TransportAntiviral AgentsRNA, MessengerCRM1host mRNAmRNA exportNPCNup98NXF1Rae1viral mRNAvirus

Identifiers

PMID37628773
PMCPMC10454920
OpenAlexW4385697499

What Socratic holds

Textmetadata
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 Socratic graph.