Evidence map›Paper›PMID 11447125›Full record

ArticleThe EMBO journal2001

Synthesis of a novel hepatitis C virus protein by ribosomal frameshift.

Z Xu, J Choi, T S Yen, W Lu, A Strohecker, S Govindarajan, D Chien, M J Selby, J Ou

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed
11.6field-weighted citation impact, top 1% 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

94 citing papers in PubMed, 276 citations in OpenAlex.

  1. Article
  2. Biomarkers of Hepatic Toxicity: An Overview.Current therapeutic research, clinical and experimental · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Hepatitis C Virus Translation Regulation.International journal of molecular sciences · 2020
    Review
  9. The Role of the RNA-RNA Interactome in the Hepatitis C Virus Life Cycle.International journal of molecular sciences · 2020
    Review
  10. Review
  11. Emergency Services of Viral RNAs: Repair and Remodeling.Microbiology and molecular biology reviews : MMBR · 2018
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Chaperones in hepatitis C virus infection.World journal of hepatology · 2016
    Review
  19. Article
  20. Article

34 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Z XuDepartment of Molecular Microbiology and Immunology, University of Southern California, 2011 Zonal Avenue, HMR-401, Los Angeles, CA 90033, USA.
J Choi
T S Yen
W Lu
A Strohecker
S Govindarajan
D Chien
M J Selby
J Ou
University of Southern California · US

Funding

TRANSGENIC MICE AS A MODEL TO STUDY HEPATITIS C VIRUS IMMUNOPATHOGENESISU19AI040038 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LAI, MICHAEL M.C. · 1996 to 2004
$3.8M
PATHOGENESIS OF CHRONIC HEPATITIS AND HEPATOMAR03AI045873 · NIAID · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI YEN, TIEN-SZE BENEDICT · 1999 to 2001
$149k
NIAID NIH HHS N01 AI040038NIAID NIH HHS R03AI45873NIAID NIH HHS U019AI40038
6 · The paper itself

Abstract

Hepatitis C virus (HCV) is an important human pathogen that affects approximately 100 million people worldwide. Its RNA genome codes for a polyprotein, which is cleaved by viral and cellular proteases to produce at least 10 mature viral protein products. We report here the discovery of a novel HCV protein synthesized by ribosomal frameshift. This protein, which we named the F protein, is synthesized from the initiation codon of the polyprotein sequence followed by ribosomal frameshift into the -2/+1 reading frame. This ribosomal frameshift requires only codons 8-14 of the core protein-coding sequence, and the shift junction is located at or near codon 11. An F protein analog synthesized in vitro reacted with the sera of HCV patients but not with the sera of hepatitis B patients, indicating the expression of the F protein during natural HCV infection. This unexpected finding may open new avenues for the development of anti-HCV drugs.

Indexed as

Frameshifting, RibosomalAmino Acid SequenceBase SequenceCodonDNA, ViralGenome, ViralHepacivirusMolecular Sequence DataOpen Reading FramesViral Core ProteinsCodonDNA, Viralhepatitis C protein F, Hepatitis C virusViral Core Proteins

Identifiers

PMID11447125
PMCPMC125543
OpenAlexW1969728880

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.