Evidence map›Paper›PMID 25613381›Full record

ArticleCell death and differentiation2015

Interplay of H2A deubiquitinase 2A-DUB/Mysm1 and the p19(ARF)/p53 axis in hematopoiesis, early T-cell development and tissue differentiation.

M Gatzka, A Tasdogan, A Hainzl, G Allies, P Maity, C Wilms, M Wlaschek, K Scharffetter-Kochanek

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Protein ubiquitination in T cell development.Frontiers in immunology · 2022
    Review
  8. Review
  9. Review
  10. Review
  11. MYSM1 Suppresses Cellular Senescence and the Aging Process to Prolong Lifespan.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
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  20. Article
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 1 country.

M GatzkaDepartment of Dermatology and Allergic Diseases, University of Ulm, Ulm 89091, Germany.
A TasdoganInstitute of Immunology, University of Ulm, Ulm 89091, Germany.
A HainzlDepartment of Dermatology and Allergic Diseases, University of Ulm, Ulm 89091, Germany.
G AlliesInstitute of Immunology, University of Ulm, Ulm 89091, Germany.
P MaityDepartment of Dermatology and Allergic Diseases, University of Ulm, Ulm 89091, Germany.
C WilmsDepartment of Dermatology and Allergic Diseases, University of Ulm, Ulm 89091, Germany.
M WlaschekDepartment of Dermatology and Allergic Diseases, University of Ulm, Ulm 89091, Germany.
K Scharffetter-KochanekDepartment of Dermatology and Allergic Diseases, University of Ulm, Ulm 89091, Germany.
Universität Ulm · DEUniversity Hospital Ulm · DETechnische Hochschule Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoubiquitination of core histone 2A (H2A-K119u) has a critical role in gene regulation in hematopoietic differentiation and other developmental processes. To explore the interplay of histone H2A deubiquitinase Myb-like SWIRM and MPN domain containing1 (2A-DUB/Mysm1) with the p53 axis in the sequential differentiation of mature lymphocytes from progenitors, we systematically analyzed hematopoiesis and early T-cell development using Mysm1(-/-) and p53(-/-)Mysm1(-/-) mice. Mysm1(-/-) thymi were severely hypoplastic with <10% of wild-type cell numbers as a result of a reduction of early thymocyte progenitors in context with defective hematopoietic stem cells, a partial block at the double-negative (DN)1-DN2 transition and increased apoptosis of double-positive thymocytes. Increased rates of apoptosis were also detected in other tissues affected by Mysm1 deficiency, including the developing brain and the skin. By quantitative PCR and chromatin immunoprecipitation analyses, we identified p19(ARF), an important regulator of p53 tumor suppressor protein levels, as a potential Mysm1 target gene. In newly generated p53(-/-)Mysm1(-/-) double-deficient mice, anomalies of Mysm1(-/-) mice including reduction of lymphoid-primed multipotent progenitors, reduced thymocyte numbers and viability, and interestingly defective B-cell development, growth retardation, neurological defects, skin atrophy, and tail malformation were almost completely restored as well, substantiating the involvement of the p53 pathway in the alterations caused by Mysm1 deficiency. In conclusion, this investigation uncovers a novel link between H2A deubiquitinase 2A-DUB/Mysm1 and suppression of p53-mediated apoptotic programs during early lymphoid development and other developmental processes.

Indexed as

AnimalsCell DifferentiationCyclin-Dependent Kinase Inhibitor p19EndopeptidasesGene Expression ProfilingHematopoiesisHistonesMaleMiceMice, Inbred C57BLMice, KnockoutT-LymphocytesTrans-ActivatorsTumor Suppressor Protein p53Ubiquitin-Specific ProteasesCyclin-Dependent Kinase Inhibitor p19Endopeptidasesgamma-H2AX protein, mouseHistonesMYSM1 protein, mouseTrans-ActivatorsTumor Suppressor Protein p53Ubiquitin-Specific Proteases

Identifiers

PMID25613381
PMCPMC4532772
OpenAlexW1990976022

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.