Evidence map›Paper›PMID 17339335›Full record

ArticleMolecular and cellular biology2007

Thymomegaly, microsplenia, and defective homeostatic proliferation of peripheral lymphocytes in p51-Ets1 isoform-specific null mice.

Tsukasa Higuchi, Frank O Bartel, Masahiro Masuya, Takao Deguchi, Kelly W Henderson, Runzhao Li, Robin C Muise-Helmericks, Michael J Kern, Dennis K Watson, Demetri D Spyropoulos

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. ETS‑1/ETS‑2 transcription factors in CVD (Review).International journal of molecular medicine · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review of Ets1 structure, function, and roles in immunity.Cellular and molecular life sciences : CMLS · 2013
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. 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

10 authors.

Tsukasa HiguchiHollings Cancer Center, Medical University of South Carolina, Charleston, SC 29425, USA.
Frank O Bartel
Masahiro Masuya
Takao Deguchi
Kelly W Henderson
Runzhao Li
Robin C Muise-Helmericks
Michael J Kern
Dennis K Watson
Demetri D Spyropoulos

Funding

UBIQUITIN CARBOXYL TERMINAL HYDROLASE L1 (UCH-L1) AND VASCULAR LESION FORMATIONP20RR016434 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 2001 to 2011
$24.8M
THE ROLE OF FLI1 IN CELLULAR DIFFERENTIATION AND DEVELOPMENTP01CA078582 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WATSON, DENNIS K · 1998 to 2009
$9.1M
Modulation of EMT by ETS1 and EAPIIK22CA109577 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LI, RUNZHAO · 2004 to 2006
$470k
NCI NIH HHS K22 CA109577NCI NIH HHS K22CA109577NCI NIH HHS P01 CA078582NCI NIH HHS P01 CA78582NCRR NIH HHS P20 RR016434NCRR NIH HHS P20 RR16434
6 · The paper itself

Abstract

Ets1 is a member of the Ets transcription factor family. Alternative splicing of exon VII results in two naturally occurring protein isoforms: full-length Ets1 (p51-Ets1) and Ets1(DeltaVII) (p42-Ets1). These isoforms bear key distinctions regarding protein-protein interactions, DNA binding kinetics, and transcriptional target specificity. Disruption of both Ets1 isoforms in mice results in the loss of detectable NK and NKT cell activity and defects in B and T lymphocytes. We generated mice that express only the Ets1(DeltaVII) isoform. Ets1(DeltaVII) homozygous mice express no p51-Ets1 and elevated levels of the p42-Ets1 protein relative to the wild type and display increased perinatal lethality, thymomegaly, and peripheral lymphopenia. Proliferation was increased in both the thymus and the spleen, while apoptosis was decreased in the thymus and increased in the spleen of homozygotes. Significant elevations of CD8(+) and CD8(+)CD4(+) thymocytes were observed. Lymphoid cell (CD19(+), CD4(+), and CD8(+)) reductions were predominantly responsible for diminished spleen cellularity, with fewer memory cells and a failure of homeostatic proliferation to maintain peripheral lymphocytes. Collectively, the Ets1(DeltaVII) mutants demonstrate lymphocyte maturation defects associated with misregulation of p16(Ink4a), p27(Kip1), and CD44. Thus, a balance in the differential regulation of Ets1 isoforms represents a potential mechanism in the control of lymphoid maturation and homeostasis.

Indexed as

HomeostasisAnimalsBase SequenceCell ProliferationCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p27Gene Expression RegulationHeterozygoteHyaluronan ReceptorsLymphocytesMiceMolecular Sequence DataPhenotypeProtein IsoformsProto-Oncogene Protein c-ets-1SpleenCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p27Hyaluronan ReceptorsProtein IsoformsProto-Oncogene Protein c-ets-1

Identifiers

PMID17339335
PMCPMC1899970

What OpenQuestion holds

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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.