Evidence map›Paper›PMID 35679955›Full record

ArticleDevelopmental biology2022

Zinc finger RNA binding protein 2 (ZFR2) is not required for male fertility in the mouse.

Lachlan M Cauchi, Brendan J Houston, Liina Nagirnaja, Anne E O'Connor, D Jo Merriner, Kenneth I Aston, Peter N Schlegel, Don F Conrad, Richard Burke, Moira K O'Bryan

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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 3 countries.

Lachlan M CauchiSchool of Biological Sciences, Monash University, Clayton, Australia; Institute for Veterinary Anatomy, Histology and Embryology, Justus-Liebig University, Giessen, Germany.
Brendan J HoustonThe School of BioSciences and Bio21 Institute, The University of Melbourne, Parkville, Australia. Electronic address: brendan.houston@unimelb.edu.au.
Liina NagirnajaOregon National Primate Research Center, Oregon Health & Science University, Oregon, USA.
Anne E O'ConnorThe School of BioSciences and Bio21 Institute, The University of Melbourne, Parkville, Australia.
D Jo MerrinerThe School of BioSciences and Bio21 Institute, The University of Melbourne, Parkville, Australia.
Kenneth I AstonAndrology and IVF Laboratory, Division of Urology, Department of Surgery, University of Utah School of Medicine, Utah, USA.
Peter N SchlegelWeill Cornell Medicine, Department of Urology, New York, USA.
Don F ConradOregon National Primate Research Center, Oregon Health & Science University, Oregon, USA.
Richard BurkeSchool of Biological Sciences, Monash University, Clayton, Australia.
Moira K O'BryanThe School of BioSciences and Bio21 Institute, The University of Melbourne, Parkville, Australia.
The University of Melbourne · AUOregon National Primate Research Center · USCornell University · USJustus-Liebig-Universität Gießen · DEMonash University · AUUniversity of Utah · US

Funding

GENOMICS OF SPERMATOGENIC IMPAIRMENTR01HD078641 · NICHD · WASHINGTON UNIVERSITY · PI Kenneth Ivan Aston, DONALD F. CONRAD · 2014 to 2026
$6.3M
NICHD NIH HHS R01 HD078641
6 · The paper itself

Abstract

backgroundThousands of genes are expressed during spermatogenesis and male infertility has a strong genetic component. Within this study, we focus on the role of Zfr2 in male fertility, a gene previously implicated in human male fertility. To date, very little is known about the role of ZFR2 in either humans or mice. To this end, the requirement for ZFR2 in male fertility was assessed using a knockout mouse model.

resultsZfr2 was found to be expressed in the testes of both humans and mice. Deletion of Zfr2 was achieved via removal of exon 2 using CRISPR-Cas9 methods. The absence of Zfr2 did not result in a reduction in any fertility parameters assessed. Knockout males were capable of fostering litter sizes equal to wild type males, and there were no effects of Zfr2 knockout on sperm number or motility. We note Zfr2 knockout females were also fertile.

conclusionsThe absence of Zfr2 alone is not sufficient to cause a reduction in male fertility in mice.

Indexed as

Infertility, MaleSemenAnimalsFemaleFertilityMaleMiceMice, KnockoutRibonucleoproteinsRNA-Binding ProteinsSpermatogenesisSpermatozoaSperm MotilityTestisZinc FingersRibonucleoproteinsRNA-Binding ProteinsZrsr2 protein, mouse

Identifiers

PMID35679955
PMCPMC12120929
OpenAlexW4281765455

What OpenQuestion holds

Textmetadata
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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.