Estienne Anthony, Lahoz Belén, Jarrier Peggy, Bodin Loys, Folch José, Alabart José-Luis, Fabre Stéphane, Monniaux Danielle
UMR85 PRC, INRA, CNRS, IFCEUniversité de Tours, Nouzilly, France.
Unidad de Producción y Sanidad AnimalCentro de Investigación y Tecnología Agroalimentaria de Aragón (CITA), Instituto Agroalimentario de Aragón - IA2 (CITA-Universidad de Zaragoza), Zaragoza, España.
Reproduction. 2017 Apr;153(4):395-404. doi: 10.1530/REP-16-0507. Epub 2017 Jan 9.
Polymorphisms in the gene encoding bone morphogenetic protein 15 (BMP15) have been associated with multiple ovulations in sheep. As BMP15 regulates inhibin expression in rodents, we assumed that the ovarian inhibin/activin system could mediate part of the effect of BMP15 mutations in the regulation of ovulation rate in sheep. To answer this question, we have studied the effects of two natural loss-of-function mutations of BMP15 on the expression of components of this system. The FecX and the FecX mutations, when present respectively in Rasa Aragonesa ewes at the heterozygous state and in Grivette ewes at the homozygous state, were associated with a twofold increase in ovulation rate. There were only small differences between mutant and wild-type ewes for mRNA expression of INHA, INHBA, ACVR1B, ACVR2A, FST or TGFBR3 in granulosa cells and inhibin A or activin A concentrations in follicular fluid. Moreover, the effects of mutations differed between breeds. In cultures of granulosa cells from wild-type ewes, BMP15, acting alone or in synergy with GDF9, stimulated INHA, INHBA and FST expression, but inhibited the expression of TGFBR3 Activin A did not affect INHBA expression, but inhibited the expression of ACVR2A also. The complexity of the inhibin/activin system, including positive and antagonistic elements, and the differential regulation of these elements by BMP15 and activin can explain that the effects of BMP15 mutations differ when present in different genetic backgrounds. In conclusion, the ovarian inhibin/activin system is unlikely to participate in the increase of ovulation rate associated with BMP15 mutations in sheep.
编码骨形态发生蛋白15(BMP15)的基因多态性与绵羊的多排卵有关。由于BMP15调节啮齿动物中的抑制素表达,我们推测卵巢抑制素/激活素系统可能介导BMP15突变在调节绵羊排卵率中的部分作用。为了回答这个问题,我们研究了BMP15的两种自然功能丧失突变对该系统成分表达的影响。FecX和FecX突变分别以杂合状态存在于阿拉贡纳绵羊母羊中以及以纯合状态存在于格里维特绵羊母羊中时,与排卵率增加两倍有关。在颗粒细胞中,INHA、INHBA、ACVR1B、ACVR2A、FST或TGFBR3的mRNA表达以及卵泡液中抑制素A或激活素A的浓度在突变型和野生型母羊之间只有微小差异。此外,突变的影响在不同品种之间有所不同。在野生型母羊颗粒细胞培养物中,BMP15单独作用或与GDF9协同作用时,刺激INHA、INHBA和FST表达,但抑制TGFBR3的表达。激活素A不影响INHBA表达,但也抑制ACVR2A的表达。抑制素/激活素系统的复杂性,包括正向和拮抗元件,以及BMP15和激活素对这些元件的差异调节,可以解释当BMP15突变存在于不同遗传背景中时其作用不同。总之,卵巢抑制素/激活素系统不太可能参与绵羊中与BMP15突变相关的排卵率增加。