Evidence map›Paper›PMID 24145430›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Plus-end tracking proteins, CLASPs, and a viral Akt mimic regulate herpesvirus-induced stable microtubule formation and virus spread.

Mojgan H Naghavi, Gregg G Gundersen, Derek Walsh

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

37 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  15. HSV-1 Cytoplasmic Envelopment and Egress.International journal of molecular sciences · 2020
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Viral journeys on the intracellular highways.Cellular and molecular life sciences : CMLS · 2018
    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

3 authors at 3 institutions in 2 countries.

Mojgan H NaghaviDepartment of Microbiology and Molecular Biophysics, College of Physicians and Surgeons, and Department of Pathology and Cell Biology, Columbia University, New York, NY 10032.
Gregg G Gundersen
Derek Walsh
Columbia University · USNew York University · USRoyal College of Physicians · GB

Funding

Virus Host Interactions that Regulate Translation in Cells Infected with HSV-1R01AI073898 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MOHR, IAN J · 2008 to 2020
$5.0M
REGULATION OF MICROTUBULES BY RHO GTPASESR01GM062939 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GUNDERSEN, GREGG G · 2001 to 2013
$4.6M
Characterization of the antiviral and nuclear regulatory functions of FEZ1 & NEK1R01GM101975 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI NAGHAVI, MOJGAN HOSSEINI · 2012 to 2016
$1.6M
NIAID NIH HHS R01 AI073898NIAID NIH HHS R01AI073898NIGMS NIH HHS R01 GM062939NIGMS NIH HHS R01GM062939NIGMS NIH HHS R01 GM101975NIGMS NIH HHS R01GM101975
6 · The paper itself

Abstract

Although microtubules (MTs) frequently form highly dynamic networks, subsets of MTs become stabilized in response to environmental cues and function as specialized tracks for vesicle and macromolecular trafficking. MT stabilization is controlled by specialized plus-end tracking proteins (+TIPs) whose accumulation at the MT ends is facilitated by the end-binding protein, EB1, and regulated by various signaling pathways. As cargoes themselves, viruses are dependent on MTs for their intracellular movement. Although many viruses affect MT organization, the potential contribution of MT stabilization by +TIPs to infection remains unknown. Here we show that early in infection of primary human fibroblasts, herpes simplex virus type 1 (HSV-1) disrupts the centrosome, the primary MT organizing center in many cell types. As infection progresses HSV-1 induces the formation of stable MT subsets through inactivation of glycogen synthase kinase 3beta by the viral Ser/Thr kinase, Us3. Stable MT formation is reduced in cells infected with Us3 mutants and those stable MTs that form cluster around the trans-Golgi network. Downstream of glycogen synthase kinase 3beta, cytoplasmic linker-associated proteins (CLASPs), specialized host +TIPs that control MT formation at the trans-Golgi network and cortical capture, are specifically required for virus-induced MT stabilization and HSV-1 spread. Our findings demonstrate the biological importance of +TIPs to viral infection and suggest that HSV-1 has evolved to exploit the trans-Golgi network as an alternate MT organizing center to facilitate virus spread.

Indexed as

Biological TransportBlotting, WesternCell Line, TumorFluorescent Antibody TechniqueGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHerpesvirus 1, HumanHumansMicrotubule-Associated ProteinsMicrotubulesRNA, Small Interferingtrans-Golgi NetworkGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGSK3B protein, humanMicrotubule-Associated ProteinsRNA, Small Interfering

Identifiers

PMID24145430
PMCPMC3831478
OpenAlexW2134812384

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.