Evidence map›Paper›PMID 25727968›Full record

ArticleStem cells (Dayton, Ohio)2015

TAF4b is required for mouse spermatogonial stem cell development.

Lindsay A Lovasco, Eric A Gustafson, Kimberly A Seymour, Dirk G de Rooij, Richard N Freiman

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.5field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Observational
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

5 authors at 2 institutions in 2 countries.

Lindsay A LovascoDepartment of Molecular and Cellular Biology and Biochemistry, Brown University, Providence, Rhode Island, USA.
Eric A Gustafson
Kimberly A Seymour
Dirk G de Rooij
Richard N Freiman
Brown University · USAcademic Medical Center · NL

Funding

WNT SIGNALING IN HEPATOCELLULAR CARCINOMAP20RR015578 · NCRR · BROWN UNIVERSITY · PI ATWOOD, WALTER J · 2000 to 2009
$22.8M
Ovarian-specific transcription networks regulated by the TFIID subunit TAF4bR01HD065445 · NICHD · BROWN UNIVERSITY · PI FREIMAN, RICHARD NEIL · 2010 to 2014
$1.6M
CENTER FOR CANCER SIGNALING NETWORKSP30RR031153 · NCRR · BROWN UNIVERSITY · PI ATWOOD, WALTER J · 2011 to 2011
$1.1M
The Role of TAF4b in Spermatogonial Stem Cell Maintenance and Self-RenewalF32HD077986 · NICHD · BROWN UNIVERSITY · PI GUSTAFSON, ERIC · 2013 to 2015
$180k
NCRR NIH HHS P20 RR015578NCRR NIH HHS P30 RR031153NICHD NIH HHS 1F32HD077986NICHD NIH HHS F32 HD077986NICHD NIH HHS R01 HD065445
6 · The paper itself

Abstract

Long-term mammalian spermatogenesis requires proper development of spermatogonial stem cells (SSCs) that replenish the testis with germ cell progenitors during adult life. TAF4b is a gonadal-enriched component of the general transcription factor complex, TFIID, which is required for the maintenance of spermatogenesis in the mouse. Successful germ cell transplantation assays into adult TAF4b-deficient host testes suggested that TAF4b performs an essential germ cell autonomous function in SSC establishment and/or maintenance. To elucidate the SSC function of TAF4b, we characterized the initial gonocyte pool and rounds of spermatogenic differentiation in the context of the Taf4b-deficient mouse testis. Here, we demonstrate a significant reduction in the late embryonic gonocyte pool and a deficient expansion of this pool soon after birth. Resulting from this reduction of germ cell progenitors is a developmental delay in meiosis initiation, as compared to age-matched controls. While GFRα1+ spermatogonia are appropriately present as Asingle and Apaired in wild-type testes, TAF4b-deficient testes display an increased proportion of long and clustered chains of GFRα1+ cells. In the absence of TAF4b, seminiferous tubules in the adult testis either lack germ cells altogether or are found to have missing generations of spermatogenic progenitor cells. Together these data indicate that TAF4b-deficient spermatogenic progenitor cells display a tendency for differentiation at the expense of self-renewal and a renewing pool of SSCs fail to establish during the critical window of SSC development.

Indexed as

Adult Stem CellsAnimalsAnimals, NewbornCell DifferentiationMaleMiceMice, Inbred C57BLMice, KnockoutSpermatogenesisSpermatogoniaTATA-Binding Protein Associated FactorsTranscription Factor TFIIDTaf4b protein, mouseTATA-Binding Protein Associated FactorsTranscription Factor TFIIDMeiosisSelf-renewalSpermatogenesisSpermatogonial stem cellsTAF4b

Identifiers

PMID25727968
PMCPMC4376611
OpenAlexW1943418900

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.