Evidence map›Paper›PMID 17724252›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2008

Cot, a novel kinase of histone H3, induces cellular transformation through up-regulation of c-fos transcriptional activity.

Hong Seok Choi, Bong Seok Kang, Jung-Hyun Shim, Yong-Yeon Cho, Bu Young Choi, Ann M Bode, Zigang Dong

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

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  16. NF-κB and cancer: a paradigm of Yin-Yang.American journal of cancer research
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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

7 authors at 2 institutions in 2 countries.

Hong Seok ChoiHormel Institute, University of Minnesota, 801 16th Ave. NE, Austin, MN 55912, USA.
Bong Seok Kang
Jung-Hyun Shim
Yong-Yeon Cho
Bu Young Choi
Ann M Bode
Zigang Dong
Hormel (United States) · USUniversity of Minnesota · US

Funding

Ultraviolet-Induced Signal TrasductionR01CA077646 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI DONG, ZIGANG · 1999 to 2010
$2.3M
Anticarcinogenic Mechanisms of Tea ConstituentsR01CA081064 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI DONG, ZIGANG · 1999 to 2007
$1.9M
Anticarcinogenic Mechanisms of Tea ConstituentsR37CA081064 · NCI · UNIVERSITY OF MINNESOTA · PI DONG, ZIGANG · 2008 to 2012
$1.5M
Inhibition of Carcinogenesis by Tea and Tea ConstituentsR01CA120388 · NCI · UNIVERSITY OF MINNESOTA · PI DONG, ZIGANG · 2006 to 2010
$1.3M
Molecular basis of arsenic-induced cell transformationR01CA111356 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI DONG, ZIGANG · 2005 to 2007
$872k
NCI NIH HHS CA111356NCI NIH HHS CA120388NCI NIH HHS CA77646NCI NIH HHS CA81064NCI NIH HHS R01 CA077646NCI NIH HHS R01 CA081064NCI NIH HHS R01 CA111356NCI NIH HHS R01 CA120388NCI NIH HHS R37 CA081064
6 · The paper itself

Abstract

Post-translational modification of histones is critical for gene expression, mitosis, cell growth, apoptosis, and cancer development. Thus, finding protein kinases that are responsible for the phosphorylation of histones at critical sites is considered an important step in understanding the process of histone modification. The serine/threonine kinase Cot is a member of the mitogen-activated protein kinase (MAPK) kinase kinase family. We show here that Cot can phosphorylate histone H3 at Ser-10 in vivo and in vitro, and that the phosphorylation of histone H3 at Ser-10 is required for Cot-induced cell transformation. We found that activated Cot is recruited to the c-fos promoter resulting in increased activator protein-1 (AP-1) transactivation. The formation of the Cot-c-fos promoter complex was also apparent when histone H3 was phosphorylated at Ser-10. Furthermore, the use of dominant negative mutants of histone H3 revealed that Cot was required for phosphorylation of histone H3 at Ser-10 to induce neoplastic cell transformation. These results revealed an important function of Cot as a newly discovered histone H3 kinase. Moreover, the transforming ability of Cot results from the coordinated activation of histone H3, which ultimately converges on the regulation of the transcriptional activity of the c-fos promoter, followed by AP-1 transactivation activity.

Indexed as

Genes, fosTranscription, GeneticUp-RegulationAnimalsBase SequenceCell LineCell Transformation, NeoplasticDNA PrimersElectrophoresis, Polyacrylamide GelEnzyme InductionHistonesHumansMiceNIH 3T3 CellsPhosphorylationPromoter Regions, GeneticDNA PrimersHistonesProtein Serine-Threonine Kinases

Identifiers

PMID17724252
PMCPMC2822465
OpenAlexW2076421117

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.