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The Initiation of Puberty in Atlantic Salmon Brings About Large Changes in Testicular Gene Expression That Are Modulated by the Energy Status

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2019 Jun 13
PMID 31185904
Citations 6
Authors
Affiliations
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Abstract

Background: When puberty starts before males reach harvest size, animal welfare and sustainability issues occur in Atlantic salmon (Salmo salar) aquaculture. Hallmarks of male puberty are an increased proliferation activity in the testis and elevated androgen production. Examining transcriptional changes in salmon testis during the transition from immature to maturing testes may help understanding the regulation of puberty, potentially leading to procedures to modulate its start. Since differences in body weight influence, via unknown mechanisms, the chances for entering puberty, we used two feed rations to create body weight differences.

Results: Maturing testes were characterized by an elevated proliferation activity of Sertoli cells and of single undifferentiated spermatogonia. Pituitary gene expression data suggest increased Gnrh receptor and gonadotropin gene expression, potentially responsible for the elevated circulating androgen levels in maturing fish. Transcriptional changes in maturing testes included a broad variety of signaling systems (e.g. Tgfβ, Wnt, insulin/Igf, nuclear receptors), but also, activation of metabolic pathways such as anaerobic metabolism and protection against ROS. Feed restriction lowered the incidence of puberty. In males maturing despite feed restriction, plasma androgen levels were higher than in maturing fish receiving the full ration. A group of 449 genes that were up-regulated in maturing fully fed fish, was up-regulated more prominently in testis from fish maturing under caloric restriction. Moreover, 421 genes were specifically up-regulated in testes from fish maturing under caloric restriction, including carbon metabolism genes, a pathway relevant for nucleotide biosynthesis and for placing epigenetic marks.

Conclusions: Undifferentiated spermatogonia and Sertoli cell populations increased at the beginning of puberty, which was associated with the up-regulation of metabolic pathways (e.g. anaerobic and ROS pathways) known from other stem cell systems. The higher androgen levels in males maturing under caloric restriction may be responsible for the stronger up-regulation of a common set of (449) maturation-associated genes, and the specific up-regulation of another set of (421) genes. The latter opened regulatory and/or metabolic options for initiating puberty despite feed restriction. As a means to reduce the incidence of male puberty in salmon, however, caloric restriction seems unsuitable.

Citing Articles

Endocrine and Transcriptome Changes Associated with Testicular Growth and Differentiation in Atlantic Salmon ( L.).

Skjold V, Afanasyev S, Burgerhout E, Sveen L, Rorvik K, Mota V Curr Issues Mol Biol. 2024; 46(6):5337-5351.

PMID: 38920991 PMC: 11202266. DOI: 10.3390/cimb46060319.


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

Andersson E, Schulz R, Almeida F, Kleppe L, Skaftnesmo K, Kjaerner-Semb E Endocrinology. 2024; 165(4).

PMID: 38298132 PMC: 10878062. DOI: 10.1210/endocr/bqae013.


Characterising the Physiological Responses of Chinook Salmon () Subjected to Heat and Oxygen Stress.

Marcoli R, Symonds J, Walker S, Battershill C, Bird S Biology (Basel). 2023; 12(10).

PMID: 37887052 PMC: 10604766. DOI: 10.3390/biology12101342.


Pituitary Gonadotropin Gene Expression During Induced Onset of Postsmolt Maturation in Male Atlantic Salmon: and Tissue Culture Studies.

Crespo D, Skaftnesmo K, Kjaerner-Semb E, Yilmaz O, Norberg B, Olausson S Front Endocrinol (Lausanne). 2022; 13:826920.

PMID: 35370944 PMC: 8964956. DOI: 10.3389/fendo.2022.826920.


Loss of Increases Germ Cell Apoptosis but Is Still Compatible With Sperm Production in Atlantic Salmon ().

Skaftnesmo K, Crespo D, Kleppe L, Andersson E, Edvardsen R, Norberg B Front Cell Dev Biol. 2021; 9:657192.

PMID: 33942021 PMC: 8087537. DOI: 10.3389/fcell.2021.657192.


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