Evidence map›Paper›PMID 24719255›Full record

ArticleBiology of reproduction2014

Riding the spermatogenic wave: profiling gene expression within neonatal germ and sertoli cells during a synchronized initial wave of spermatogenesis in mice.

Elizabeth Evans, Cathryn Hogarth, Debra Mitchell, Michael Griswold

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
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  5. Cell cycle regulation for meiosis in mammalian germ cells.The Journal of reproduction and development · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. Review
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  12. Review
  13. Article
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  15. Article
  16. Transcriptomics of Meiosis in the Male Mouse.Frontiers in cell and developmental biology · 2021
    Review
  17. Article
  18. Whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model.DNA research : an international journal for rapid publication of reports on genes and genomes · 2020
    Article
  19. Review
  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

4 authors at 1 institution in 1 country.

Elizabeth EvansSchool of Molecular Biosciences and The Center for Reproductive Biology, Washington State University, Pullman, Washington.
Cathryn HogarthSchool of Molecular Biosciences and The Center for Reproductive Biology, Washington State University, Pullman, Washington.
Debra MitchellSchool of Molecular Biosciences and The Center for Reproductive Biology, Washington State University, Pullman, Washington.
Michael GriswoldSchool of Molecular Biosciences and The Center for Reproductive Biology, Washington State University, Pullman, Washington mgriswold@wsu.edu.
Washington State University · US

Funding

Hormonal Regulation Sertoli Cell MaturationR01HD010808 · NICHD · WASHINGTON STATE UNIVERSITY · PI MICHAEL D GRISWOLD · 1985 to 2026
$6.0M
HORMONAL REGULATION OF SERTOLI CELL MATURATIONR37HD010808 · NICHD · WASHINGTON STATE UNIVERSITY · PI GRISWOLD, MICHAEL D · 1997 to 2006
$1.8M
Molecular Bioscience Graduate Training ProgramT32GM083864 · NIGMS · WASHINGTON STATE UNIVERSITY · PI NILSON, JOHN H. · 2010 to 2014
$646k
NICHD NIH HHS HD 10808NICHD NIH HHS R01 HD010808NICHD NIH HHS R37 HD010808NIGMS NIH HHS 5T32GM083864NIGMS NIH HHS T32 GM083864PHS HHS U54 42454
6 · The paper itself

Abstract

Continual sperm production relies on germ cells undergoing spermatogenesis asynchronously. As a result, the testis always contains a mixed population of germ cells at different stages of their differentiation process. The heterogeneous nature of the testis makes profiling gene expression within Sertoli cells or specific populations of germ cells impossible when a wild-type testis is assessed. We recently reported a unique method for synchronizing spermatogenesis without affecting fertility by manipulating RA levels within the neonatal testis. Using this protocol, combined with the RiboTag transgenic mouse line, we have mapped the Sertoli and germ cell translatome during the initial synchronized wave of spermatogenesis. Using microarray analysis, we identified 392 and 194 germ cell and Sertoli cells transcripts, respectively, that dynamically change during spermatogonial differentiation, division, and the onset of meiosis. Functional annotation clustering revealed that transcripts enriched in germ cells were mostly associated with meiosis (21 transcripts), chromatin organization (12 transcripts), and cell cycle (3 transcripts). In addition, glycoproteins (65 transcripts), cell adhesion (15 transcripts), and cell junction (13 transcripts) transcripts were overrepresented in the Sertoli cell-enriched list. These datasets represent the first transcriptional analysis of spermatogonial differentiation, division, and meiotic onset. These data suggest that several of the genes encoding meiotic proteins are expressed and are actively being translated well before germ cells enter meiosis. In addition, this study provides novel candidate genes, Asf1b and Esyt3, that may be involved in the regulation of spermatogonial chromatin reorganization, germ-Sertoli cell interactions, and/or blood-testis barrier formation.

Indexed as

AnimalsAnimals, NewbornComputational BiologyDiaminesFemaleGene Expression ProfilingGene Expression Regulation, DevelopmentalImmunohistochemistryMaleMice, KnockoutMice, TransgenicOligonucleotide Array Sequence AnalysisRNASertoli CellsSpermatogenesisSpermatogoniaDiaminesN,N'-bis(dichloroacetyl)-1,8-octamethylenediamineRNATretinoingene expressiongerm cellsretinoic acidretinoidsSertoli cellsspermatogoniatestistranslational profiling

Identifiers

PMID24719255
PMCPMC4076369
OpenAlexW2169148057

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.