Evidence map›Paper›PMID 22275078›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2012

TEG-1 CD2BP2 regulates stem cell proliferation and sex determination in the C. elegans germ line and physically interacts with the UAF-1 U2AF65 splicing factor.

Chris Wang, Laura Wilson-Berry, Tim Schedl, Dave Hansen

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2012. 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
1.3field-weighted citation impact, top 24% 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, 31 citations in OpenAlex.

  1. Article
  2. ADR-2 regulates fertility and oocyte fate inbioRxiv : the preprint server for biology · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Article
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  8. Article
  9. Review
  10. Biology of theGenetics · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Stem cell proliferation versus meiotic fate decision in Caenorhabditis elegans.Advances in experimental medicine and biology · 2013
    Review
  17. Review
  18. 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

4 authors at 2 institutions in 2 countries.

Chris WangUniversity of Calgary, Department of Biological Sciences, Alberta, Calgary, Canada.
Laura Wilson-Berry
Tim Schedl
Dave Hansen
University of Calgary · CAWashington University in St. Louis · US

Funding

Stem cell proliferation / meiosis decision in C. elegansR01GM063310 · NIGMS · WASHINGTON UNIVERSITY · PI SCHEDL, TIM · 2001 to 2008
$3.2M
CIHRNIGMS NIH HHS GM63310NIGMS NIH HHS R01 GM063310
6 · The paper itself

Abstract

backgroundFor a stem cell population to exist over an extended period, a balance must be maintained between self-renewing (proliferating) and differentiating daughter cells. Within the Caenorhabditis elegans germ line, this balance is controlled by a genetic regulatory pathway, which includes the canonical Notch signaling pathway.

resultsGenetic screens identified the gene teg-1 as being involved in regulating the proliferation versus differentiation decision in the C. elegans germ line. Cloning of TEG-1 revealed that it is a homolog of mammalian CD2BP2, which has been implicated in a number of cellular processes, including in U4/U6.U5 tri-snRNP formation in the pre-mRNA splicing reaction. The position of teg-1 in the genetic pathway regulating the proliferation versus differentiation decision, its single mutant phenotype, and its enrichment in nuclei, all suggest TEG-1 also functions as a splicing factor. TEG-1, as well as its human homolog, CD2BP2, directly bind to UAF-1 U2AF65, a component of the U2 auxiliary factor.

conclusionsTEG-1 functions as a splicing factor and acts to regulate the proliferation versus meiosis decision. The interaction of TEG-1 CD2BP2 with UAF-1 U2AF65, combined with its previously described function in U4/U6.U5 tri-snRNP, suggests that TEG-1 CD2BP2 functions in two distinct locations in the splicing cascade.

Indexed as

Cell ProliferationSex Determination ProcessesAdaptor Proteins, Signal TransducingAllelesAlternative SplicingAmino Acid SequenceAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCarrier ProteinsCell DifferentiationCell NucleusFemaleGerm CellsHumansMaleAdaptor Proteins, Signal TransducingCaenorhabditis elegans ProteinsCarrier ProteinsCD2BP2 protein, humanNuclear ProteinsRibonucleoproteinsRNA Splicing FactorsSplicing Factor U2AFTEG-1 protein, C elegansU2AF2 protein, humanUAF-1 protein, C elegans

Identifiers

PMID22275078
PMCPMC3466600
OpenAlexW1968287982

What OpenQuestion holds

Textmetadata
LicenceTDM
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.