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

Author:

Crespo Diego1ORCID,Fjelldal Per Gunnar2ORCID,Hansen Tom J.2ORCID,Kjærner‐Semb Erik1ORCID,Skaftnesmo Kai Ove1ORCID,Thorsen Anders1ORCID,Norberg Birgitta3ORCID,Edvardsen Rolf B.1ORCID,Andersson Eva1ORCID,Schulz Rüdiger W.14ORCID,Wargelius Anna1ORCID,Kleppe Lene1ORCID

Affiliation:

1. Research Group Reproduction and Developmental Biology Institute of Marine Research Bergen Norway

2. Research Group Reproduction and Developmental Biology Institute of Marine Research, Matre Research Station Matredal Norway

3. Research Group Reproduction and Developmental Biology Institute of Marine Research, Austevoll Research Station Haukanes Norway

4. Reproductive Biology Group, Division Developmental Biology, Department Biology, Science Faculty Utrecht University Utrecht The Netherlands

Abstract

AbstractBone 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.

Funder

Norges Forskningsråd

Publisher

Wiley

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