Evidence map›Paper›PMID 35618043›Full record

ArticleDevelopmental biology2022

IRGC1, a testis-enriched immunity related GTPase, is important for fibrous sheath integrity and sperm motility in mice.

Yuki Kaneda, Haruhiko Miyata, Keisuke Shimada, Yuki Oyama, Rie Iida-Norita, Masahito Ikawa

Open access · hybridAbstract 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Identification of protein candidates in spermatozoa of water buffalo (Frontiers in cell and developmental biology · 2023
    Article
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 2 institutions in 1 country.

Yuki KanedaResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka, 5650871, Japan; Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka, 5650871, Japan. Electronic address: kaneda-y@biken.osaka-u.ac.jp.
Haruhiko MiyataResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka, 5650871, Japan. Electronic address: hmiya003@biken.osaka-u.ac.jp.
Keisuke ShimadaResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka, 5650871, Japan. Electronic address: shimada-k@biken.osaka-u.ac.jp.
Yuki OyamaResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka, 5650871, Japan; Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka, 5650871, Japan. Electronic address: oyama-y@biken.osaka-u.ac.jp.
Rie Iida-NoritaResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka, 5650871, Japan. Electronic address: iida-r@biken.osaka-u.ac.jp.
Masahito IkawaResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka, 5650871, Japan; Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka, 5650871, Japan; The Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo, 1088639, Japan; Center for Infectious Disease Education and Research, Osaka University, 2-8 Yamadaoka, Suita, Osaka, 5650871, Japan. Electronic address: ikawa@biken.osaka-u.ac.jp.
The University of Osaka · JPThe University of Tokyo · JP

Funding

Targeting sperm-specific proteins during meiosis and sperm morphogenesisP01HD087157 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI GARCIA, THOMAS · 2017 to 2021
$6.2M
Functional analysis of novel testis-expressed secreted and transmembrane proteinsR01HD088412 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI MARTIN M. MATZUK · 2016 to 2026
$4.5M
NICHD NIH HHS P01 HD087157NICHD NIH HHS R01 HD088412
6 · The paper itself

Abstract

Immunity-related GTPases (IRGs), also known as p47 GTPases, are a family of interferon-inducible proteins that play roles in immunity defense against intracellular pathogens. Although the molecular functions of IRGs have been well studied, the function of the family member, IRGC1, remains unclear. IRGC1 is unique among IRGs because its expression is not induced by interferon and it is expressed predominantly in the testis. Further, IRGC1 is well conserved in mammals unlike other IRGs. Here, we knocked out (KO) Irgc1 in mice using the CRISPR/Cas9 system and found that the fertility of Irgc1 KO males was severely impaired because of abnormal sperm motility. Further analyses with a transmission electron microscope revealed that the fibrous sheath (FS), an accessory structure of the sperm tail, was disorganized in Irgc1 KO mice. In addition, IRGC1 was detected in the sperm tail and fractionated with FS proteins. These results suggest that IRGC1 is a component of the FS and is involved in the correct formation of the FS.

Indexed as

Sperm MotilityTestisAnimalsGTP PhosphohydrolasesInterferonsMaleMammalsMiceMice, KnockoutProteinsSpermatozoaSperm TailGTP PhosphohydrolasesInterferonsIrgc1 protein, mouseProteinsCRISPR/Cas9Fibrous sheathFlagellump47 GTPasesSperm motility

Identifiers

PMID35618043
PMCPMC9232189
OpenAlexW4281288111

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.