Evidence map›Paper›PMID 20980392›Full record

ArticleJournal of cell science2010

Transcriptional regulation of ferritin and antioxidant genes by HIPK2 under genotoxic stress.

Kiros Hailemariam, Kenta Iwasaki, Bo-Wen Huang, Kensuke Sakamoto, Yoshiaki Tsuji

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
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  7. Down-regulation of ATF1 leads to early neuroectoderm differentiation of human embryonic stem cells by increasing the expression level of SOX2.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  8. Article
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  11. Review
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  13. Article
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  15. Article
  16. Ferritin upregulates hepatic expression of bone morphogenetic protein 6 and hepcidin in mice.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Article
  17. Article
  18. 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

5 authors at 3 institutions in 2 countries.

Kiros HailemariamDepartment of Environmental and Molecular Toxicology, North Carolina State University, Campus Box 7633, Raleigh, NC 27695, USA.
Kenta Iwasaki
Bo-Wen Huang
Kensuke Sakamoto
Yoshiaki Tsuji
North Carolina State University · USNagoya University · JPUnited States Food and Drug Administration · US

Funding

TRAINING IN BIOCHEMICAL AND ENVIRONMENTAL TOXICOLOGYT32ES007046 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Seth William Kullman · 1985 to 2026
$5.1M
REGULATION OF IRON HOMEOSTASIS IN OXIDATIVE STRESSR01DK060007 · NIDDK · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI TSUJI, YOSHIAKI · 2002 to 2005
$1.2M
NIDDK NIH HHS DK-60007NIDDK NIH HHS DK-60007SNIDDK NIH HHS R01 DK060007NIEHS NIH HHS ES-007046NIEHS NIH HHS T32 ES007046
6 · The paper itself

Abstract

ATF1 (activating transcription factor 1), a stimulus-induced CREB family transcription factor, plays important roles in cell survival and proliferation. Phosphorylation of ATF1 at Ser63 by PKA (cAMP-dependent protein kinase) and related kinases was the only known post-translational regulatory mechanism of ATF1. Here, we found that HIPK2 (homeodomain-interacting protein kinase 2), a DNA-damage-responsive nuclear kinase, is a new ATF1 kinase that phosphorylates Ser198 but not Ser63. ATF1 phosphorylation by HIPK2 activated ATF1 transcription function in the GAL4-reporter system. ATF1 is a transcriptional repressor of ferritin H, the major intracellular iron storage gene, through an ARE (antioxidant-responsive element). HIPK2 overrode the ATF1-mediated ARE repression in a kinase-activity-dependent manner in HepG2 cells. Furthermore, DNA-damage-inducing agents doxorubicin, etoposide and sodium arsenite induced ferritin H mRNA expression in HIPK2(+/+) MEF cells, whereas it was significantly impaired in HIPK2(-/-) MEF cells. Induction of other ARE-regulated detoxification genes such as NQO1 (NADPH quinone oxidoreductase 1), GST (glutathione S-transferase) and HO1 (heme oxygenase 1) by genotoxic stress was also decreased in HIPK2-deficient cells. Taken together, these results suggest that HIPK2 is a new ATF1 kinase involved in the regulation of ferritin H and other antioxidant detoxification genes in genotoxic stress conditions.

Indexed as

DNA DamageActivating Transcription Factor 1Carrier ProteinsCell Growth ProcessesCell SurvivalFerritinsGene Expression RegulationHumansPhosphorylationProtein Serine-Threonine KinasesTranscription FactorsActivating Transcription Factor 1Carrier ProteinsFerritinsHIPK2 protein, humanProtein Serine-Threonine KinasesTranscription Factors

Identifiers

PMID20980392
PMCPMC2972272
OpenAlexW1986956929

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.