Evidence map›Paper›PMID 37882691›Full record

ArticleDevelopment (Cambridge, England)2023

The katanin A-subunits KATNA1 and KATNAL1 act co-operatively in mammalian meiosis and spermiogenesis to achieve male fertility.

Jessica E M Dunleavy, Maddison Graffeo, Kathryn Wozniak, Anne E O'Connor, D Jo Merriner, Joseph Nguyen, Ralf B Schittenhelm, Brendan J Houston, Moira K O'Bryan

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. 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

9 authors at 3 institutions in 1 country.

Jessica E M DunleavySchool of BioSciences and Bio21 Institute, Faculty of Science, The University of Melbourne, Melbourne, VIC 3010, Australia.ORCID 0000-0003-2009-0165
Maddison GraffeoSchool of BioSciences and Bio21 Institute, Faculty of Science, The University of Melbourne, Melbourne, VIC 3010, Australia.
Kathryn WozniakMonash Biomedicine Discovery Institute and The Department of Anatomy and Developmental Biology, Monash University, Melbourne, VIC 3800, Australia.ORCID 0009-0000-7729-2556
Anne E O'ConnorSchool of BioSciences and Bio21 Institute, Faculty of Science, The University of Melbourne, Melbourne, VIC 3010, Australia.
D Jo MerrinerSchool of BioSciences and Bio21 Institute, Faculty of Science, The University of Melbourne, Melbourne, VIC 3010, Australia.
Joseph NguyenSchool of BioSciences and Bio21 Institute, Faculty of Science, The University of Melbourne, Melbourne, VIC 3010, Australia.
Ralf B SchittenhelmMonash Proteomics & Metabolomics Facility, Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.
Brendan J HoustonSchool of BioSciences and Bio21 Institute, Faculty of Science, The University of Melbourne, Melbourne, VIC 3010, Australia.ORCID 0000-0002-1078-756X
Moira K O'BryanSchool of BioSciences and Bio21 Institute, Faculty of Science, The University of Melbourne, Melbourne, VIC 3010, Australia.ORCID 0000-0001-7298-4940
The University of Melbourne · AUAustralian Regenerative Medicine Institute · AUMonash University · AU

Funding

Australian Research Council DP160100647Male Contraceptive InitiativeNational Health and Medical Research Council APP1180929The University of Melbourne
6 · The paper itself

Abstract

Katanins, a class of microtubule-severing enzymes, are potent M-phase regulators in oocytes and somatic cells. How the complex and evolutionarily crucial, male mammalian meiotic spindle is sculpted remains unknown. Here, using multiple single and double gene knockout mice, we reveal that the canonical katanin A-subunit KATNA1 and its close paralogue KATNAL1 together execute multiple aspects of meiosis. We show KATNA1 and KATNAL1 collectively regulate the male meiotic spindle, cytokinesis and midbody abscission, in addition to diverse spermatid remodelling events, including Golgi organisation, and acrosome and manchette formation. We also define KATNAL1-specific roles in sperm flagellum development, manchette regulation and sperm-epithelial disengagement. Finally, using proteomic approaches, we define the KATNA1, KATNAL1 and KATNB1 mammalian testis interactome, which includes a network of cytoskeletal and vesicle trafficking proteins. Collectively, we reveal that the presence of multiple katanin A-subunit paralogs in mammalian spermatogenesis allows for 'customised cutting' via neofunctionalisation and protective buffering via gene redundancy.

Indexed as

KataninMicrotubulesProteomicsAnimalsFertilityMaleMeiosisMiceSemenSpermatogenesisKataninKatna1 protein, mouseKatnal1 protein, mouseAcrosomeAxonemeHead-to-tail coupling apparatusKataninManchetteMeiotic spindleMicrotubule severingSpermatogenesisSpermiationVesicle transport

Identifiers

PMID37882691
PMCPMC10690054
OpenAlexW4387948568

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.