Evidence map›Paper›PMID 26501274›Full record

ArticleInternational journal of molecular sciences2015

CRISPR/Cas9-Mediated Rapid Generation of Multiple Mouse Lines Identified Ccdc63 as Essential for Spermiogenesis.

Samantha A M Young, Haruhiko Miyata, Yuhkoh Satouh, Hirotaka Kato, Kaori Nozawa, Ayako Isotani, R John Aitken, Mark A Baker, Masahito Ikawa

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
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  8. International journal of molecular sciences · 2023
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  19. Sperm proteins SOF1, TMEM95, and SPACA6 are required for sperm-oocyte fusion in mice.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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 2 institutions in 2 countries.

Samantha A M YoungSchool of Environmental and Life Science, University of Newcastle, Callaghan, New South Wales 2308, Australia. samantha.a.young@uon.edu.au.
Haruhiko MiyataResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan. hmiya003@biken.osaka-u.ac.jp.
Yuhkoh SatouhResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan. yuhkohs@biken.osaka-u.ac.jp.
Hirotaka KatoResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan. hkato@biken.osaka-u.ac.jp.
Kaori NozawaResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan. nozawak@biken.osaka-u.ac.jp.
Ayako IsotaniImmunology Frontier Research Center, Osaka University, Suita, Osaka 565-0871, Japan. isotani@biken.osaka-u.ac.jp.
R John AitkenSchool of Environmental and Life Science, University of Newcastle, Callaghan, New South Wales 2308, Australia. john.aitken@newcastle.edu.au.
Mark A BakerSchool of Environmental and Life Science, University of Newcastle, Callaghan, New South Wales 2308, Australia. mark.baker@newcastle.edu.au.
Masahito IkawaResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan. ikawa@biken.osaka-u.ac.jp.
The University of Osaka · JPUniversity of Newcastle Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spermatozoa are flagellated cells whose role in fertilization is dependent on their ability to move towards an oocyte. The structure of the sperm flagella is highly conserved across species, and much of what is known about this structure is derived from studies utilizing animal models. One group of proteins essential for the movement of the flagella are the dyneins. Using the advanced technology of CRISPR/Cas9 we have targeted three dynein group members; Dnaic1, Wdr63 and Ccdc63 in mice. All three of these genes are expressed strongly in the testis. We generated mice with amino acid substitutions in Dnaic1 to analyze two specific phosphorylation events at S124 and S127, and generated simple knockouts of Wdr63 and Ccdc63. We found that the targeted phosphorylation sites in Dnaic1 were not essential for male fertility. Similarly, Wdr63 was not essential for male fertility; however, Ccdc63 removal resulted in sterile male mice due to shortened flagella. This study demonstrates the versatility of the CRISPR/Cas9 system to generate animal models of a highly complex system by introducing point mutations and simple knockouts in a fast and efficient manner.

Indexed as

AnimalsCRISPR-Cas SystemsMaleMiceSpermatogenesisSperm Motilitygenome editingspermatogenesissperm motilitytargeted mutagenesis

Identifiers

PMID26501274
PMCPMC4632774
OpenAlexW2163989499

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.