Evidence map›Paper›PMID 19004954›Full record

ArticleJournal of virology2009

hnRNPs Relocalize to the cytoplasm following infection with vesicular stomatitis virus.

Elizabeth L Pettit Kneller, John H Connor, Douglas S Lyles

Abstract read
In one paragraph

Article in Journal of virology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

44 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Viral Modulation of Host Splicing.Annual review of virology · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Seneca Valley Virus 3CFrontiers in microbiology · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. 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

3 authors at 2 institutions in 1 country.

Elizabeth L Pettit KnellerDepartment of Biochemistry, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, North Carolina 27157, USA.
John H Connor
Douglas S Lyles
Wake Forest University · USBoston University · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Control of translation by VSVR01AI052304 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LYLES, DOUGLAS S. · 2004 to 2008
$1.2M
Control of translation by VSVR21AI052304 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LYLES, DOUGLAS S. · 2003 to 2003
$288k
Control of elF4F complex by Vesicular Stomatitis VirusK22AI064606 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CONNOR, JOHN H · 2006 to 2007
$270k
INFLUENZA VIRUS EFFECTS ON MACROPHAGE VESICLE TRAFFICR01AI035892 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI LOWY, ROBERT J · 1994 to 1996
–
NCI NIH HHS CA12197NCI NIH HHS P30 CA012197NIAID NIH HHS AI064606NIAID NIH HHS AI35892NIAID NIH HHS AI52304NIAID NIH HHS K22 AI064606NIAID NIH HHS R01 AI052304NIAID NIH HHS R21 AI052304
6 · The paper itself

Abstract

Vesicular stomatitis virus (VSV) matrix protein inhibits nuclear-cytoplasmic mRNA transport. The goal of this work is to determine whether VSV inhibits the nuclear-cytoplasmic transport of heterogeneous ribonucleoproteins (hnRNPs), which are thought to serve as mRNA export factors. Confocal microscopy experiments showed that hnRNPA1, hnRNPK, and hnRNPC1/C2, but not hnRNPB1 or lamin A/C, are relocalized to the cytoplasm during VSV infection. We determined whether protein import is inhibited by VSV by transfecting cells with a plasmid encoding enhanced green fluorescent protein (EGFP) tagged with either the M9 nuclear localization sequence (NLS) or the classical NLS. These experiments revealed that both the M9 NLS and the classical NLS are functional during VSV infection. These data suggest that the inhibition of protein import is not responsible for hnRNP relocalization during VSV infection but that hnRNP export is enhanced. We found that hnRNPA1 relocalization was significantly reduced following the silencing of the mRNA export factor Rae1, indicating that Rae1 is necessary for hnRNP export. In order to determine the role of hnRNPA1 in VSV infection, we silenced hnRNPA1 in HeLa cells and assayed three aspects of the viral life cycle: host protein synthesis shutoff concurrent with the onset of viral protein synthesis, replication by plaque assay, and cell killing. We observed that host shutoff and replication are unaffected by the reduction in hnRNPA1 but that the rate of VSV-induced apoptosis is slower in cells that have reduced hnRNPA1. These data suggest that VSV promotes hnRNPA1 relocalization in a Rae1-dependent manner for apoptotic signaling.

Indexed as

Virus ReplicationApoptosisCytoplasmGene SilencingHeLa CellsHeterogeneous-Nuclear RibonucleoproteinsHumansMicroscopy, ConfocalNuclear Matrix-Associated ProteinsNucleocytoplasmic Transport ProteinsVesiculovirusViral Plaque AssayHeterogeneous-Nuclear RibonucleoproteinsNuclear Matrix-Associated ProteinsNucleocytoplasmic Transport ProteinsRAE1 protein, human

Identifiers

PMID19004954
PMCPMC2612367
OpenAlexW2170871049

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.