Evidence map›Paper›PMID 10995483›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

The role of cdc2 in the expression of herpes simplex virus genes.

S J Advani, R R Weichselbaum, B Roizman

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. 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
5.6field-weighted citation impact, top 4% 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, 67 citations in OpenAlex.

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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 1 institution in 1 country.

S J AdvaniThe Marjorie B. Kovler Viral Oncology Laboratories, and Department of Radiation and Cellular Oncology, University of Chicago, 910 East 58th Street, Chicago, IL 60637, USA.
R R Weichselbaum
B Roizman
University of Chicago · US

Funding

Virus Production CoreP01CA071933 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WEICHSELBAUM, RALPH R · 1997 to 2013
$14.5M
Dissection Of The Functions Of Herpes Simplex Virus ICPOR37CA078766 · NCI · UNIVERSITY OF CHICAGO · PI ROIZMAN, BERNARD · 2003 to 2012
$4.4M
DISSECTION OF THE FUNCTIONS OF HERPES SIMPLEX VIRUS ICPOR01CA078766 · NCI · UNIVERSITY OF CHICAGO · PI ROIZMAN, BERNARD · 1998 to 2002
$1.1M
MOLECULAR BIOLOGY OF HERPES SIMPLEX VIRUSESR35CA047451 · NCI · UNIVERSITY OF CHICAGO · PI ROIZMAN, BERNARD · 1988 to 2000
$910k
NCI NIH HHS CA47451NCI NIH HHS CA71933NCI NIH HHS CA78766NCI NIH HHS P01 CA071933NCI NIH HHS R01 CA078766NCI NIH HHS R37 CA078766
6 · The paper itself

Abstract

Earlier reports have shown that cdc2 kinase is activated in cells infected with herpes simplex virus 1 and that the activation is mediated principally by two viral proteins, the infected cell protein 22 (ICP22) and the protein kinase encoded by U(L)13. The same proteins are required for optimal expression of a subset of late (gamma(2)) genes exemplified by U(S)11. In this study, we used a dominant-negative cdc2 protein to determine the role of cdc2 in viral gene expression. We report the following. (i) The cdc2 dominant-negative protein had no effect in the synthesis and accumulation of at least two alpha-regulatory proteins (ICP4 and ICP0), two beta-proteins (ribonucleotide reductase major subunit and single-stranded DNA-binding protein), and two gamma(1)-proteins (glycoprotein D and viral protease). U(S)11, a gamma(2)-protein, accumulated only in cells in which cdc2 dominant-negative protein could not be detected or was made in very small amounts. (ii) The sequence of amino acids predicted to be phosphorylated by cdc2 is present in at least 27 viral proteins inclusive of the regulatory proteins ICP4, ICP0, and ICP22. In in vitro assays, we demonstrated that cdc2 specifically phosphorylated a polypeptide consisting of the second exon of ICP0 but not a polypeptide containing the sequence of the third exon as would be predicted from the sequence analysis. We conclude that cdc2 is required for optimal expression of a subset of gamma(2)-proteins whose expression is also regulated by the viral proteins (ICP22 and U(L)13) that mediate the activation of cdc2 kinase.

Indexed as

Gene Expression Regulation, ViralCDC2 Protein KinaseEnzyme ActivationHeLa CellsHerpes SimplexHumansSimplexvirusVirus ReplicationCDC2 Protein Kinase

Identifiers

PMID10995483
PMCPMC27137
OpenAlexW2001500656

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.