Evidence map›Paper›PMID 33635866›Full record

ArticlePLoS genetics2021

Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility.

Isabella Aprea, Johanna Raidt, Inga Marlena Höben, Niki Tomas Loges, Tabea Nöthe-Menchen, Petra Pennekamp, Heike Olbrich, Thomas Kaiser, Luisa Biebach, Frank Tüttelmann and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
14.0field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. A Case of Primary Ciliary Dyskinesia Caused byCase reports in medicine · 2026
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Case Report: Minigene assays reveal a novelFrontiers in genetics · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Primary Ciliary Dyskinesia.Pediatrics · 2024
    Review
  20. [Primary ciliary dyskinesia].Innere Medizin (Heidelberg, Germany) · 2024
    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

15 authors at 1 institution in 1 country.

Isabella ApreaDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0001-5681-874X
Johanna RaidtDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-1571-2647
Inga Marlena HöbenDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-1133-6496
Niki Tomas LogesDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-1534-2105
Tabea Nöthe-MenchenDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-0571-6767
Petra PennekampDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-8202-3809
Heike OlbrichDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.
Thomas KaiserDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-6699-0014
Luisa BiebachDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0003-2863-4841
Frank TüttelmannInstitute of Reproductive Genetics, University of Muenster, Muenster, Germany.ORCID 0000-0003-2745-9965
Judit HorvathInstitute of Human Genetics, University Hospital Muenster, Muenster, Germany.
Maria SchubertDepartment of Clinical and Surgical Andrology, Centre of Reproductive Medicine and Andrology, University Hospital Muenster, Muenster, Germany.ORCID 0000-0001-8548-9551
Claudia KrallmannDepartment of Clinical and Surgical Andrology, Centre of Reproductive Medicine and Andrology, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-3679-0628
Sabine KlieschInstitute of Human Genetics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-7561-4870
Heymut OmranDepartment of General Pediatrics, University Hospital Muenster, Muenster, Germany.ORCID 0000-0003-0282-6765
University Hospital Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Axonemal protein complexes, such as outer (ODA) and inner (IDA) dynein arms, are responsible for the generation and regulation of flagellar and ciliary beating. Studies in various ciliated model organisms have shown that axonemal dynein arms are first assembled in the cell cytoplasm and then delivered into axonemes during ciliogenesis. In humans, mutations in genes encoding for factors involved in this process cause structural and functional defects of motile cilia in various organs such as the airways and result in the hereditary disorder primary ciliary dyskinesia (PCD). Despite extensive knowledge about the cytoplasmic assembly of axonemal dynein arms in respiratory cilia, this process is still poorly understood in sperm flagella. To better define its clinical relevance on sperm structure and function, and thus male fertility, further investigations are required. Here we report the fertility status in different axonemal dynein preassembly mutant males (DNAAF2/ KTU, DNAAF4/ DYX1C1, DNAAF6/ PIH1D3, DNAAF7/ZMYND10, CFAP300/C11orf70 and LRRC6). Besides andrological examinations, we functionally and structurally analyzed sperm flagella of affected individuals by high-speed video- and transmission electron microscopy as well as systematically compared the composition of dynein arms in sperm flagella and respiratory cilia by immunofluorescence microscopy. Furthermore, we analyzed the flagellar length in dynein preassembly mutant sperm. We found that the process of axonemal dynein preassembly is also critical in sperm, by identifying defects of ODAs and IDAs in dysmotile sperm of these individuals. Interestingly, these mutant sperm consistently show a complete loss of ODAs, while some respiratory cilia from the same individual can retain ODAs in the proximal ciliary compartment. This agrees with reports of solely one distinct ODA type in sperm, compared to two different ODA types in proximal and distal respiratory ciliary axonemes. Consistent with observations in model organisms, we also determined a significant reduction of sperm flagellar length in these individuals. These findings are relevant to subsequent studies on the function and composition of sperm flagella in PCD patients and non-syndromic infertile males. Our study contributes to a better understanding of the fertility status in PCD-affected males and should help guide genetic and andrological counselling for affected males and their families.

Indexed as

Axonemal DyneinsAxonemeCiliaCohort StudiesCytoplasmCytoskeletal ProteinsFlagellaHumansInfertility, MaleIntracellular Signaling Peptides and ProteinsMaleMicroscopy, Electron, TransmissionMutationNerve Tissue ProteinsSpermatozoaAxonemal DyneinsCFAP300 protein, humanCytoskeletal ProteinsDNAAF11 protein, humanDNAAF4 protein, humanDNAAF6 protein, humanIntracellular Signaling Peptides and ProteinsNerve Tissue Proteins

Identifiers

PMID33635866
PMCPMC7909641
OpenAlexW3129493904

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.