Evidence map›Paper›PMID 16840350›Full record

ArticleJournal of virology2006

A poxvirus host range protein, CP77, binds to a cellular protein, HMG20A, and regulates its dissociation from the vaccinia virus genome in CHO-K1 cells.

Jye-Chian Hsiao, Chien-Chiang Chao, Ming-Jer Young, Yu-Tai Chang, Er-Chieh Cho, Wen Chang

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2006. 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
1.0field-weighted citation impact, top 28% 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, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Evaluation of Viral Genome Copies Within Viral Factories on Different DNA Viruses.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2018
    Article
  11. Article
  12. Production of a Chikungunya Vaccine Using a CHO Cell and Attenuated Viral-Based Platform Technology.Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    Article
  13. Review
  14. Article
  15. The Role of F-Box Proteins during Viral Infection.International journal of molecular sciences · 2013
    Article
  16. The poxvirus C7L host range factor superfamily.Current opinion in virology · 2012
    Review
  17. Article
  18. Article
  19. Addition of poly(A) and poly(A)-rich tails during RNA degradation in the cytoplasm of human cells.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  20. Poxvirus proteomics and virus-host protein interactions.Microbiology and molecular biology reviews : MMBR · 2009
    Review
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 2 institutions in 2 countries.

Jye-Chian HsiaoGraduate Institute of Life Sciences, National Defense Medical Center, Nankang, Taipei, Taiwan.
Chien-Chiang Chao
Ming-Jer Young
Yu-Tai Chang
Er-Chieh Cho
Wen Chang
Institute of Molecular Biology, Academia Sinica · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vaccinia virus does not grow in Chinese hamster ovary (CHO-K1) cells in the absence of a viral host range factor, cowpox protein CP77. In this study, CP77 was fused to the C terminus of green fluorescence protein (GFP-CP77) and a series of nested deletion mutants of GFP-CP77 was constructed for insertion into a vaccinia virus host range mutant, VV-hr, and expressed from a viral early promoter. Deletion mapping analyses demonstrated that the N-terminal 352 amino acids of CP77 were sufficient to support vaccinia virus growth in CHO-K1 cells, whereas the C-terminal residues 353 to 668 were dispensable. In yeast two-hybrid analyses, CP77 bound to a cellular protein, HMG20A, and GST pulldown analyses showed that residues 1 to 234 of CP77 were sufficient for this interaction. After VV-hr virus infection of CHO-K1 cells, HMG20A was translocated from the nucleus to viral factories and bound to the viral genome via the HMG box region. In control VV-hr-infected CHO-K1 cells, binding of HMG20A to the viral genome persisted from 2 to 8 h postinfection (h p.i.); in contrast, when CP77 was expressed, the association of HMG20A with viral genome was transient, with little HMG20A remaining bound at 8 h p.i. This indicates that dissociation of HMG20A from viral factories correlates well with CP77 host range activity in CHO-K1 cells. Finally, in cells expressing a CP77 deletion protein (amino acids 277 to 668) or a DeltaANK5 mutant that did not support vaccinia virus growth and did not contain the HMG20A binding site, HMG20A remained bound to viral DNA, demonstrating that the binding of CP77 to HMG20A is essential for its host range function. In summary, our data revealed that a novel cellular protein, HMG20A, the dissociation of which from viral DNA is regulated by CP77, providing the first cellular target regulated by viral host range CP77 protein.

Indexed as

Gene Expression Regulation, ViralGenome, ViralAnimalsBinding SitesCHO CellsCricetinaeDNA, ViralHigh Mobility Group ProteinsHumansPoxviridaeSaccharomyces cerevisiaeSequence DeletionTwo-Hybrid System TechniquesVaccinia virusViral ProteinsDNA, ViralHigh Mobility Group ProteinsHMG20A protein, humanViral Proteins

Identifiers

PMID16840350
PMCPMC1563734
OpenAlexW2103477288

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.