Evidence map›Paper›PMID 38298132›Full record

ArticleEndocrinology2024

Loss of Fshr Prevents Testicular Maturation in Atlantic Salmon (Salmo salar L.).

Eva Andersson, Rüdiger W Schulz, Fernanda Almeida, Lene Kleppe, Kai Ove Skaftnesmo, Erik Kjærner-Semb, Diego Crespo, Per Gunnar Fjelldal, Tom Johnny Hansen, Birgitta Norberg and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

4 citing papers in PubMed, 17 citations in OpenAlex.

  1. Germ cell manipulation in farmed fishes.The Journal of reproduction and development · 2026
    Review
  2. Generation of IgMScientific reports · 2025
    Article
  3. Article
  4. 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

12 authors at 3 institutions in 4 countries.

Eva AnderssonInstitute of Marine Research, NO-5817 Bergen, Norway.ORCID 0000-0002-7864-1014
Rüdiger W SchulzInstitute of Marine Research, NO-5817 Bergen, Norway.ORCID 0000-0001-9115-669X
Fernanda AlmeidaEmbrapa Amazônia Ocidental, 69010-97 Manaus, Amazonas, Brazil.ORCID 0000-0003-3507-2808
Lene KleppeInstitute of Marine Research, NO-5817 Bergen, Norway.
Kai Ove SkaftnesmoInstitute of Marine Research, NO-5817 Bergen, Norway.
Erik Kjærner-SembInstitute of Marine Research, NO-5817 Bergen, Norway.
Diego CrespoInstitute of Marine Research, NO-5817 Bergen, Norway.
Per Gunnar FjelldalInstitute of Marine Research, NO-5817 Bergen, Norway.ORCID 0000-0001-9237-2706
Tom Johnny HansenInstitute of Marine Research, NO-5817 Bergen, Norway.
Birgitta NorbergInstitute of Marine Research, NO-5817 Bergen, Norway.
Rolf B EdvardsenInstitute of Marine Research, NO-5817 Bergen, Norway.
Anna WargeliusInstitute of Marine Research, NO-5817 Bergen, Norway.
Norwegian Institute of Marine Research · NOBrazilian Agricultural Research Corporation · BRUniversity of Applied Sciences Utrecht · NL

Funding

Research Council of Norway 267610
6 · The paper itself

Abstract

Early puberty poses a significant challenge for male Atlantic salmon in aquaculture due to its negative impact on growth and welfare. The regulation of puberty in vertebrates involves 2 key reproductive hormones: follicle-stimulating hormone (FSH) and luteinizing hormone (LH) and their gonadal receptors. In male mice lacking FSH receptor, testes size is reduced, but fertility is maintained, while medaka and zebrafish with a disrupted fshr gene exhibit near normal testis size and fertility. In these fishes both Fsh and Lh are present during puberty and Lh may rescue fertility, while in salmonid fish only Fsh is present in the circulation during puberty. Using CRISPR-Cas9, we produced crispants with a high prevalence of fshr mutations at the target site, which remained fertile, although more than half showed a testis development deviating from wild-type (wt) males. Crossing out these F0 crispants to each other produced a viable F1 generation showing frameshift (fshr-/-) or in-frame mutations (fshrif/if). Nearly all wt males matured while all fshr-/- males remained immature with small testes containing A spermatogonia as the furthest developed germ cell type and prepubertal plasma androgen levels. Also, the pituitary transcript levels of gnrhr2bba and lhb, but not for fshb, were reduced in the fshr-/- males compared with maturing males. More than half of the fshrif/if mutant males showed no or a delayed maturation. In conclusion, Atlantic salmon show the unique characteristic that loss of Fshr function alone results in male infertility, offering new opportunities to control precocious puberty or fertility in salmon.

Indexed as

Receptors, FSHSalmo salarAnimalsFollicle Stimulating HormoneMaleMiceSexual MaturationTestisZebrafishFollicle Stimulating HormoneReceptors, FSHaquacultureCRISPR-Cas9FSH receptorpubertysterility

Identifiers

PMID38298132
PMCPMC10878062
OpenAlexW4391441832

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.