Evidence map›Paper›PMID 31729367›Full record

ArticleNature communications2019

Sertoli cell-only phenotype and scRNA-seq define PRAMEF12 as a factor essential for spermatogenesis in mice.

Zhengpin Wang, Xiaojiang Xu, Jian-Liang Li, Cameron Palmer, Dragan Maric, Jurrien Dean

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
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  3. Male germ cell-specific deletion ofZoological research · 2026
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  7. Single-cell analysis of adult mouse testes exposed to cigarette smoke.Journal of assisted reproduction and genetics · 2026
    Article
  8. Male infertility.Systems biology in reproductive medicine · 2025
    Review
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  12. Review
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  14. Article
  15. 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

6 authors at 1 institution in 1 country.

Zhengpin WangLaboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda, MD, 20892, USA. zhengpin.wang@nih.gov.ORCID http://orcid.org/0000-0001-5388-1516
Xiaojiang XuIntegrative Bioinformatics, NIEHS, National Institutes of Health, Research Triangle Park, NC, 27709, USA.
Jian-Liang LiIntegrative Bioinformatics, NIEHS, National Institutes of Health, Research Triangle Park, NC, 27709, USA.ORCID http://orcid.org/0000-0002-6487-081X
Cameron PalmerLaboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda, MD, 20892, USA.
Dragan MaricNINDS Flow Cytometry Core Facility, National Institutes of Health, Bethesda, MD, 20892, USA.
Jurrien DeanLaboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda, MD, 20892, USA. jurrien.dean@nih.gov.ORCID http://orcid.org/0000-0002-7127-0871
National Institutes of Health · US

Funding

Molecular Biology of the OocyteZIADK015603 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI DEAN, JURRIEN · 2009 to 2025
$43.2M
6 · The paper itself

Abstract

Spermatogonial stem cells (SSCs) have the dual capacity to self-renew and differentiate into progenitor spermatogonia that develop into mature spermatozoa. Here, we document that preferentially expressed antigen of melanoma family member 12 (PRAMEF12) plays a key role in maintenance of the spermatogenic lineage. In male mice, genetic ablation of Pramef12 arrests spermatogenesis and results in sterility which can be rescued by transgenic expression of Pramef12. Pramef12 deficiency globally decreases expression of spermatogenic-related genes, and single-cell transcriptional analysis of post-natal male germline cells identifies four spermatogonial states. In the absence of Pramef12 expression, there are fewer spermatogonial stem cells which exhibit lower expression of SSC maintenance-related genes and are defective in their ability to differentiate. The disruption of the first wave of spermatogenesis in juvenile mice results in agametic seminiferous tubules. These observations mimic a Sertoli cell-only syndrome in humans and may have translational implications for reproductive medicine.

Indexed as

SpermatogenesisAnimalsIntracellular Signaling Peptides and ProteinsMaleMiceMice, Inbred C57BLMice, TransgenicPhenotypeSequence Analysis, RNASertoli CellsSpermatogoniaIntracellular Signaling Peptides and ProteinsPramef12 protein, mouse

Identifiers

PMID31729367
PMCPMC6858368
OpenAlexW2985679201

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.