Evidence map›Paper›PMID 33442887›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2021

The Sertoli cell expressed gene secernin-1 (Scrn1) is dispensable for male fertility in the mouse.

Brendan J Houston, Liina Nagirnaja, D Jo Merriner, Anne E O'Connor, Hidenobu Okuda, Kenan Omurtag, Craig Smith, Kenneth I Aston, Donald F Conrad, Moira K O'Bryan

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

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  5. Genetic mutation ofLife science alliance · 2024
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  6. Cell genomics · 2023
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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

10 authors at 6 institutions in 2 countries.

Brendan J HoustonSchool of Biological Sciences, Monash University, Clayton, Victoria, Australia.ORCID 0000-0002-1078-756X
Liina NagirnajaDivision of Genetics, Oregon National Primate Research Center, Beaverton, Oregon, USA.
D Jo MerrinerSchool of Biological Sciences, Monash University, Clayton, Victoria, Australia.
Anne E O'ConnorSchool of Biological Sciences, Monash University, Clayton, Victoria, Australia.
Hidenobu OkudaSchool of Biological Sciences, Monash University, Clayton, Victoria, Australia.
Kenan OmurtagDivision of Reproductive Endocrinology and Infertility, School of Medicine, Washington University, St Louis, Missouri, USA.
Craig SmithBiomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Kenneth I AstonDepartment of Surgery (Urology), University of Utah, Salt Lake City, Utah, USA.
Donald F ConradDivision of Genetics, Oregon National Primate Research Center, Beaverton, Oregon, USA.
Moira K O'BryanSchool of Biological Sciences, Monash University, Clayton, Victoria, Australia.ORCID 0000-0001-7298-4940
Monash University · AUOregon National Primate Research Center · USThe University of Melbourne · AUAustralian Regenerative Medicine Institute · AUUniversity of Utah · USWashington University in St. Louis · US

Funding

Project IIIP50HD096723 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Kyle Edwin Orwig · 2019 to 2026
$15.0M
NICHD NIH HHS P50 HD096723
6 · The paper itself

Abstract

backgroundMale infertility is a prevalent clinical presentation for which there is likely a strong genetic component due to the thousands of genes required for spermatogenesis. Within this study we investigated the role of the gene Scrn1 in male fertility. Scrn1 is preferentially expressed in XY gonads during the period of sex determination and in adult Sertoli cells based on single cell RNA sequencing. We investigated the expression of Scrn1 in juvenile and adult tissues and generated a knockout mouse model to test its role in male fertility.

resultsScrn1 was expressed at all ages examined in the post-natal testis; however, its expression peaked at postnatal days 7-14 and SCRN1 protein was clearly localized to Sertoli cells. Scrn1 deletion was achieved via removal of exon 3, and its loss had no effect on male fertility or sex determination. Knockout mice were capable of siring litters of equal size to wild type counterparts and generated equal numbers of sperm with comparable motility and morphology characteristics.

conclusionsScrn1 was found to be dispensable for male fertility, but this study identifies SCRN1 as a novel marker of the Sertoli cell cytoplasm.

Indexed as

AnimalsEmbryo, MammalianFemaleFertilityInfertility, MaleMaleMiceMice, Inbred C57BLMice, KnockoutNerve Tissue ProteinsPregnancySertoli CellsSpermatogenesisTestisNerve Tissue Proteinssecernin 1 protein, mousesertoli cellsex developmentspermatogenesis

Identifiers

PMID33442887
PMCPMC9012169
OpenAlexW3118671263

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.