Evidence map›Paper›PMID 19966288›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

JNK-mediated turnover and stabilization of the transcription factor p45/NF-E2 during differentiation of murine erythroleukemia cells.

Tung-Liang Lee, Yu-Chiau Shyu, Pang-Hung Hsu, Chiung-Wen Chang, Shau-Ching Wen, Wei-Yuan Hsiao, Ming-Daw Tsai, Che-Kun James Shen

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. c-Jun NHHepatology (Baltimore, Md.) · 2020
    Article
  5. Bach1: Function, Regulation, and Involvement in Disease.Oxidative medicine and cellular longevity · 2018
    Review
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  7. Article
  8. Review
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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

8 authors at 3 institutions in 2 countries.

Tung-Liang LeeInstitute of Molecular Biology, Academia Sinica, Taipei 115, Taiwan, Republic of China.
Yu-Chiau Shyu
Pang-Hung Hsu
Chiung-Wen Chang
Shau-Ching Wen
Wei-Yuan Hsiao
Ming-Daw Tsai
Che-Kun James Shen
Institute of Molecular Biology, Academia Sinica · TWGenomics Research Center, Academia Sinica · TWNational Defense Medical Center · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulation of the homeostatic concentrations of specific sets of transcription factors is essential for correct programming of cell proliferation and differentiation. We have characterized the signal transduction pathways regulating the catabolisis of p45/NF-E2, a bZIP factor activating the erythroid and megakaryocytic gene transcription. Through use of different approaches including nano-scale proteomics, we show that activated-JNK, or Phospho-JNK (P-JNK), physically interacts with p45/NF-E2 and phosphorylates its Ser157 residue. This reaction leads to the poly-ubiquitination of p45/NF-E2 at one or more of six Lys residues, one of which being also a sumoylation site, and its degradation through the proteasome pathway. Significantly, this regulatory pathway of p45/NF-E2 by P-JNK exists only in uninduced murine erythroleukemia (MEL) cells but not in differentiated MEL cells in which JNK is inactivated on DMSO induction. Based on the above data and analysis of the chromatin-binding kinetics of p45/NF-E2 and the erythroid gene repressor Bach1 during the early phase of MEL differentiation, we suggest a model for the regulation of erythroid maturation. In the model, the posttranslational modifications and turnover of p45/NF-E2, as mediated by P-JNK, contribute to the control of its homeostatic concentration and consequently, its regulatory functions in the progression of erythroid differentiation and erythroid gene expression.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBasic-Leucine Zipper Transcription FactorsCell DifferentiationCell Line, TumorFanconi Anemia Complementation Group ProteinsGene Expression Regulation, LeukemicHumansJNK Mitogen-Activated Protein KinasesLeukemia, Erythroblastic, AcuteMiceNF-E2 Transcription Factor, p45 SubunitPhosphorylationProteasome Endopeptidase ComplexRecombinant Fusion ProteinsSignal TransductionBACH1 protein, humanBasic-Leucine Zipper Transcription FactorsFanconi Anemia Complementation Group ProteinsJNK Mitogen-Activated Protein KinasesNF-E2 Transcription Factor, p45 SubunitProteasome Endopeptidase ComplexRecombinant Fusion Proteins

Identifiers

PMID19966288
PMCPMC2806728
OpenAlexW2123703113

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.