Evidence map›Paper›PMID 29324788›Full record

ArticlePloS one2018

Esrp1 is a marker of mouse fetal germ cells and differentially expressed during spermatogenesis.

Shaghayegh Saeidi, Farnaz Shapouri, Robb U de Iongh, Franca Casagranda, Jessie M Sutherland, Patrick S Western, Eileen A McLaughlin, Mary Familari, Gary R Hime

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. The Impact ofAnimals : an open access journal from MDPI · 2025
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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

9 authors at 4 institutions in 2 countries.

Shaghayegh SaeidiDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, Australia.
Farnaz ShapouriDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, Australia.
Robb U de IonghDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, Australia.
Franca CasagrandaDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, Australia.
Jessie M SutherlandSchool of Biomedical Sciences and Pharmacy, University of Newcastle, Callaghan, Australia.
Patrick S WesternCentre for Genetic Diseases, Hudson Institute of Medical Research and Department of Molecular and Translational Science, Monash University, Clayton, Australia.
Eileen A McLaughlinSchool of Environmental and Life Sciences, University of Newcastle, Callaghan, Australia.
Mary FamilariSchool of Biosciences, University of Melbourne, Parkville, Australia.
Gary R HimeDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, Australia.ORCID 0000-0003-4732-3184
The University of Melbourne · AUHudson Institute of Medical Research · AUUniversity of Auckland · NZUniversity of Newcastle Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ESRP1 regulates alternative splicing, producing multiple transcripts from its target genes in epithelial tissues. It is upregulated during mesenchymal to epithelial transition associated with reprogramming of fibroblasts to iPS cells and has been linked to pluripotency. Mouse fetal germ cells are the founders of the adult gonadal lineages and we found that Esrp1 mRNA was expressed in both male and female germ cells but not in gonadal somatic cells at various stages of gonadal development (E12.5-E15.5). In the postnatal testis, Esrp1 mRNA was highly expressed in isolated cell preparations enriched for spermatogonia but expressed at lower levels in those enriched for pachytene spermatocytes and round spermatids. Co-labelling experiments with PLZF and c-KIT showed that ESRP1 was localized to nuclei of both Type A and B spermatogonia in a speckled pattern, but was not detected in SOX9+ somatic Sertoli cells. No co-localization with the nuclear speckle marker, SC35, which has been associated with post-transcriptional splicing, was observed, suggesting that ESRP1 may be associated with co-transcriptional splicing or have other functions. RNA interference mediated knockdown of Esrp1 expression in the seminoma-derived Tcam-2 cell line demonstrated that ESRP1 regulates alternative splicing of mRNAs in a non-epithelial cell germ cell tumour cell line.

Indexed as

Alternative SplicingAnimalsCell Line, TumorCells, CulturedFemaleGene ExpressionGerm CellsMaleMice, Inbred C57BLRNA-Binding ProteinsRNA, MessengerSpermatogenesisTestisESRP1 protein, mouseRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID29324788
PMCPMC5764326
OpenAlexW2782692514

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.