Evidence map›Paper›PMID 33724408›Full record

ArticleGenetics2021

Infertility due to defective sperm flagella caused by an intronic deletion in DNAH17 that perturbs splicing.

Adéla Nosková, Maya Hiltpold, Fredi Janett, Thomas Echtermann, Zih-Hua Fang, Xaver Sidler, Christin Selige, Andreas Hofer, Stefan Neuenschwander, Hubert Pausch

Open access · greenAbstract read
In one paragraph

Article in Genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 3 institutions in 1 country.

Adéla NoskováAnimal Genomics, Institute of Agricultural Sciences, ETH Zürich, 8315 Lindau, Switzerland.
Maya HiltpoldAnimal Genomics, Institute of Agricultural Sciences, ETH Zürich, 8315 Lindau, Switzerland.
Fredi JanettClinic of Reproductive Medicine, Vetsuisse Faculty, University of Zurich, 8057 Zurich, Switzerland.
Thomas EchtermannDivision of Swine Medicine, Vetsuisse Faculty, University of Zurich, 8057 Zurich, Switzerland.
Zih-Hua FangAnimal Genomics, Institute of Agricultural Sciences, ETH Zürich, 8315 Lindau, Switzerland.
Xaver SidlerDivision of Swine Medicine, Vetsuisse Faculty, University of Zurich, 8057 Zurich, Switzerland.
Christin SeligeSUISAG, 6204 Sempach, Switzerland.
Andreas HoferSUISAG, 6204 Sempach, Switzerland.
Stefan NeuenschwanderAnimal Genetics, Institute of Agricultural Science, ETH Zürich, 8092 Zürich, Switzerland.
Hubert PauschAnimal Genomics, Institute of Agricultural Sciences, ETH Zürich, 8315 Lindau, Switzerland.
ETH Zurich · CHUniversity of Zurich · CHSuisag (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Artificial insemination in pig (Sus scrofa domesticus) breeding involves the evaluation of the semen quality of breeding boars. Ejaculates that fulfill predefined quality requirements are processed, diluted and used for inseminations. Within short time, eight Swiss Large White boars producing immotile sperm that had multiple morphological abnormalities of the sperm flagella were noticed at a semen collection center. The eight boars were inbred on a common ancestor suggesting that the novel sperm flagella defect is a recessive trait. Transmission electron microscopy cross-sections revealed that the immotile sperm had disorganized flagellar axonemes. Haplotype-based association testing involving microarray-derived genotypes at 41,094 SNPs of six affected and 100 fertile boars yielded strong association (P = 4.22 × 10-15) at chromosome 12. Autozygosity mapping enabled us to pinpoint the causal mutation on a 1.11 Mb haplotype located between 3,473,632 and 4,587,759 bp. The haplotype carries an intronic 13-bp deletion (Chr12:3,556,401-3,556,414 bp) that is compatible with recessive inheritance. The 13-bp deletion excises the polypyrimidine tract upstream exon 56 of DNAH17 (XM_021066525.1: c.8510-17_8510-5del) encoding dynein axonemal heavy chain 17. Transcriptome analysis of the testis of two affected boars revealed that the loss of the polypyrimidine tract causes exon skipping which results in the in-frame loss of 89 amino acids from DNAH17. Disruption of DNAH17 impairs the assembly of the flagellar axoneme and manifests in multiple morphological abnormalities of the sperm flagella. Direct gene testing may now be implemented to monitor the defective allele in the Swiss Large White population and prevent the frequent manifestation of a sterilizing sperm tail disorder in breeding boars.

Indexed as

Gene DeletionRNA SplicingAnimalsAxonemal DyneinsHaplotypesInfertility, MaleMalePolymorphism, Single NucleotideSperm TailSwineAxonemal Dyneinsexon skippinggenetic disorderGenetics of Seximpaired male fertilitypolypyrimidine tractsperm flagella defect

Identifiers

PMID33724408
PMCPMC8045731
OpenAlexW3126200546

What OpenQuestion holds

Textmetadata
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.