Evidence map›Paper›PMID 17415412›Full record

ArticleThe Journal of clinical investigation2007

Ewing sarcoma gene EWS is essential for meiosis and B lymphocyte development.

Hongjie Li, Wendy Watford, Cuiling Li, Alissa Parmelee, Mark A Bryant, Chuxia Deng, John O'Shea, Sean Bong Lee

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

82 citing papers in PubMed, 156 citations in OpenAlex.

  1. Molecular basis of EWS interdomain self-association and its role in condensate formation.Protein science : a publication of the Protein Society · 2025
    Article
  2. Phase separation of the oncogenic fusion protein EWS::FLI1 is modulated by its DNA-binding domain.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Identification of FSH-regulated and estrous stage-specific transcriptional networks in mouse ovaries.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. International journal of molecular sciences · 2024
    Review
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  15. Potential Involvement ofAnimals : an open access journal from MDPI · 2022
    Article
  16. Gammaherpesvirus-mediated repression reveals EWSR1 to be a negative regulator of B cell responses.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Article
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22 more citing papers are in PubMed but not listed here.

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.

Hongjie LiGenetics of Development and Disease Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892, USA.
Wendy Watford
Cuiling Li
Alissa Parmelee
Mark A Bryant
Chuxia Deng
John O'Shea
Sean Bong Lee
Institut thématique Génétique, génomique et bioinformatique · FRNational Institute of Arthritis and Musculoskeletal and Skin Diseases · USNational Institute of Diabetes and Digestive and Kidney Diseases · US

Funding

Stat transcription factors in immunoregulation and autoimmune diseaseZIAAR041159 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI O'SHEA, JOHN · 2009 to 2025
$49.3M
Targeting Janus kinases in the treatment of autoimmune diseaseZIAAR041106 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI O'SHEA, JOHN · 2009 to 2024
$4.8M
Targeting Jak3 in the treatment of autoimmune diseaseZ01AR041106 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI O'SHEA, JOHN J. · 1995 to 2008
$2.7M
Stat transcription factors in immunoregulation and autoimmune diseaseZ01AR041159 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI O'SHEA, JOHN · 2008 to 2008
$1.8M
Physiological roles of Ewings Sarcoma gene product EWSZIADK056005 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LEE, SEAN · 2009 to 2012
$1.7M
Mouse models of Desmoplastic Small Round Cell Tumor and Ewings sarcomaZIADK056003 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LEE, SEAN · 2009 to 2012
$1.7M
Characterization Of Wilms Tumor Suppressor Gene Product Wt1ZIADK056002 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LEE, SEAN · 2009 to 2012
$1.5M
Physiological roles of Ewings Sarcoma gene product EWSZ01DK056005 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LEE, SEAN · 2007 to 2008
$821k
Mouse models of Desmoplastic Small Round Cell Tumor and Ewings sarcomaZ01DK056003 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LEE, SEAN B. · 2005 to 2008
$821k
Characterization Of Wilms Tumor Suppressor Gene Product Wt1Z01DK056002 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LEE, SEAN B. · 2002 to 2008
$703k
Characterization of mice carrying mutations of BRCA1 interacting proteinsZ01DK056007 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI DENG, CHUXIA · 2007 to 2008
$505k
Intramural NIH HHS
6 · The paper itself

Abstract

Ewing sarcoma gene EWS encodes a putative RNA-binding protein with proposed roles in transcription and splicing, but its physiological role in vivo remains undefined. Here, we have generated Ews-deficient mice and demonstrated that EWS is required for the completion of B cell development and meiosis. Analysis of Ews(-/-) lymphocytes revealed a cell-autonomous defect in precursor B lymphocyte (pre-B lymphocyte) development. During meiosis, Ews-null spermatocytes were deficient in XY bivalent formation and showed reduced meiotic recombination, resulting in massive apoptosis and complete arrest in gamete maturation. Inactivation of Ews in mouse embryonic fibroblasts resulted in premature cellular senescence, and the mutant animals showed hypersensitivity to ionizing radiation. Finally, we showed that EWS interacts with lamin A/C and that loss of EWS results in a reduced lamin A/C expression. Our findings reveal essential functions for EWS in pre-B cell development and meiosis, with proposed roles in DNA pairing and recombination/repair mechanisms. Furthermore, we demonstrate a novel role of EWS in cellular senescence, possibly through its interaction and modulation of lamin A/C.

Indexed as

AnimalsAnimals, NewbornB-Lymphocyte SubsetsCell DifferentiationCell Line, TumorEmbryonic Stem CellsFemaleHeLa CellsHumansMaleMeiosisMiceMice, Inbred C57BLMice, KnockoutRetrospective StudiesRNA-Binding Protein EWSRNA-Binding Protein EWS

Identifiers

PMID17415412
PMCPMC1838927
OpenAlexW2105542427

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.