Evidence map›Paper›PMID 32317665›Full record

ArticleScientific reports2020

SOX3 promotes generation of committed spermatogonia in postnatal mouse testes.

Dale McAninch, Juho-Antti Mäkelä, Hue M La, James N Hughes, Robin Lovell-Badge, Robin M Hobbs, Paul Q Thomas

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. 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
4.4field-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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  11. The role of p53 in male infertility.Frontiers in endocrinology · 2024
    Review
  12. Article
  13. The Role of SOX Transcription Factors in Ageing and Age-Related Diseases.International journal of molecular sciences · 2023
    Review
  14. Article
  15. Article
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  17. Leveraging a natural murine meiotic drive to suppress invasive populations.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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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

7 authors at 4 institutions in 3 countries.

Dale McAninchSchool of Biological Sciences and Robinson Research Institute, University of Adelaide, Adelaide, SA, 5005, Australia.
Juho-Antti Mäkelä *Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, 3800, Australia.ORCID http://orcid.org/0000-0001-8489-8724
Hue M La *Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, 3800, Australia.ORCID http://orcid.org/0000-0003-4549-7017
James N HughesSchool of Biological Sciences and Robinson Research Institute, University of Adelaide, Adelaide, SA, 5005, Australia.
Robin Lovell-BadgeLaboratory of Stem Cell Biology and Developmental Genetics, The Francis Crick Institute, London, NW1 1AT, UK.ORCID http://orcid.org/0000-0001-9364-4179
Robin M HobbsAustralian Regenerative Medicine Institute, Monash University, Melbourne, VIC, 3800, Australia. robin.hobbs@monash.edu.ORCID http://orcid.org/0000-0002-3853-2614
Paul Q ThomasSchool of Biological Sciences and Robinson Research Institute, University of Adelaide, Adelaide, SA, 5005, Australia. paul.thomas@adelaide.edu.au.
The University of Adelaide · AUAustralian Regenerative Medicine Institute · AUDiscovery Institute · USThe Francis Crick Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SOX3 is a transcription factor expressed within the developing and adult nervous system where it mostly functions to help maintain neural precursors. Sox3 is also expressed in other locations, notably within the spermatogonial stem/progenitor cell population in postnatal testis. Independent studies have shown that Sox3 null mice exhibit a spermatogenic block as young adults, the mechanism of which remains poorly understood. Using a panel of spermatogonial cell marker genes, we demonstrate that Sox3 is expressed within the committed progenitor fraction of the undifferentiated spermatogonial pool. Additionally, we use a Sox3 null mouse model to define a potential role for this factor in progenitor cell function. We demonstrate that Sox3 expression is required for transition of undifferentiated cells from a GFRα1+ self-renewing state to the NGN3 + transit-amplifying compartment. Critically, using chromatin immunoprecipitation, we demonstrate that SOX3 binds to a highly conserved region in the Ngn3 promoter region in vivo, indicating that Ngn3 is a direct target of SOX3. Together these studies indicate that SOX3 functions as a pro-commitment factor in spermatogonial stem/progenitor cells.

Indexed as

Gene Expression Regulation, DevelopmentalPromoter Regions, GeneticAdult Germline Stem CellsAnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationDNA-Binding ProteinsGlial Cell Line-Derived Neurotrophic Factor ReceptorsMaleMiceMice, KnockoutNerve Tissue ProteinsPromyelocytic Leukemia Zinc Finger ProteinProtein BindingSignal TransductionSOXB1 Transcription FactorsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsGfra1 protein, mouseGlial Cell Line-Derived Neurotrophic Factor ReceptorsNerve Tissue ProteinsNeurog3 protein, mousePromyelocytic Leukemia Zinc Finger ProteinSall4 protein, mouseSox3 protein, mouseSOXB1 Transcription FactorsTranscription FactorsZbtb16 protein, mouse

Identifiers

PMID32317665
PMCPMC7174399
OpenAlexW3016369387

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.