Loss of bmp15 function in the seasonal spawner Atlantic salmon results in ovulatory failure

• Published in: The FASEB journal 2024-07, Vol.38 (14), p.e23837-n/a
• Main Authors: Crespo, Diego, Fjelldal, Per Gunnar, Hansen, Tom J., Kjærner‐Semb, Erik, Skaftnesmo, Kai Ove, Thorsen, Anders, Norberg, Birgitta, Edvardsen, Rolf B., Andersson, Eva, Schulz, Rüdiger W., Wargelius, Anna, Kleppe, Lene
• Format: Article
• Language: English
• Subjects: Animals; Atlantic salmon; bone morphogenetic protein 15; Bone Morphogenetic Protein 15 - genetics; Bone Morphogenetic Protein 15 - metabolism; CRISPR/Cas9; Female; Fish Proteins - genetics; Fish Proteins - metabolism; Male; Oocytes - metabolism; oogenesis; Ovarian Follicle - metabolism; Ovary - metabolism; Ovulation; Salmo salar - genetics; Salmo salar - growth & development; Salmo salar - metabolism; Seasons
• ISSN: 0892-6638; 1530-6860; 1530-6860
• DOI: 10.1096/fj.202400370R

Bone morphogenetic protein 15 (BMP15) is an oocyte‐specific growth factor important for successful female reproduction in mammals. While mutations in BMP15/Bmp15 cause ovulatory deficiency and/or infertility in certain mammalian species, loss of bmp15 in zebrafish, a continuous spawner and the only bmp15 knockout model in fish to date, results in complete arrest of follicle development and later female‐to‐male sex reversal, preventing to examine effects on ovulation/fertilization. Here, we used Atlantic salmon, a seasonal spawner, and generated bmp15 mutants to investigate ovarian development and fertility. Histological and morphometric analyses revealed that in biallelic frameshift (bmp15 fs/fs) mutant ovaries, folliculogenesis started earlier, resulting in an advanced development compared to wild‐type (WT) controls, accompanied by a weaker expression of the (early) oocyte‐specific factor figla. This precocious ovarian development was followed in bmp15 fs/fs females by enhanced follicle atresia during vitellogenic stages. Although genes involved in steroid synthesis and signaling (star, cyp11b, cyp17a1 and esr1) were dramatically higher in late vitellogenic bmp15 fs/fs mutant ovaries, estradiol‐17β plasma levels were lower than in WT counterparts, potentially reflecting compensatory changes at the level of ovarian gene expression. At spawning, bmp15 fs/fs females displayed lower gonado‐somatic index values and reduced oocyte diameter, and the majority (71.4%), showed mature non‐ovulating ovaries with a high degree of atresia. The remaining (28.6%) females spawned eggs but they either could not be fertilized or, upon fertilization, showed severe malformations and embryonic mortality. Our results show that Bmp15 is required for proper follicle recruitment and growth and later ovulatory success in Atlantic salmon, providing an alternative candidate target to induce sterility in farmed salmon. Moreover, since loss of bmp15 in salmon, in contrast to zebrafish, does not result in female‐to‐male sex change, this is the first mutant model in fish allowing further investigations on Bmp15‐mediated functions in the ovulatory period. Schematic illustration showing the main stages of Atlantic salmon oogenesis affected in bmp15 fs/fs mutant females. Phenotypic defects observed in bmp15 fs/fs females, including sampling points (red arrowheads) and stage of ovarian development. bmp15 fs/fs females displayed a precocious development during the secondary growth phase follo