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Bioscientifica Proceedings (2019) 5 RDRRDR27 | DOI: 10.1530/biosciprocs.5.027

REDR2002 Reproduction in Domestic Ruminants V Genes Controlling Reproductive Performance (4 abstracts)

Bone morphogenetic proteins and folliculogenesis: lessons from the Booroola mutation

CJH Souza 1 , BK Campbell 2 , AS McNeilly 3 & DT Baird 1


1Department of Reproductive and Developmental Sciences, University of Edinburgh, Centre for Reproductive Biology, 49 Little France Crescent, Edinburgh EH16 4SB, UK; 2School of Human Development, University of Nottingham, D Floor East Block, Queen's Medical Centre, Nottingham NG7 2UH, UK; and 3MRC Human Reproductive Sciences Unit, Centre for Reproductive Biology, 49 Little France Crescent, Edinburgh EH16 4SB, UK


The Booroola phenotype is associated with a point mutation in the kinase domain of the bone morphogenetic protein receptor 1B (BMPR1B), and is characterized by 'precocious' differentiation of ovarian follicles, leading to the production of large numbers of ovulatory follicles that are smaller in diameter than wild-type follicles. These smaller follicles attain differentiation markers, such as expression of mRNA for P450aromatase and inhibin-ßA subunit, granulosa cell LH receptors and aromatase activity, earlier than follicles from wild-type ewes. However, the preovulatory follicles from mutant ewes collectively secrete similar quantities of oestradiol, androstenedione and inhibin A in exactly the same pattern as wild-type ewes, which result in similar concentrations of FSH. The available evidence strongly indicates that the Booroola mutation exerts its action at the ovary rather than by altering gonadotrophin secretion. The bone morphogenetic protein (BMP) receptors and putative ligands are ubiquitously expressed within the ovary and BMPs seem to be involved in the paracrine regulation of FSH action. Thus, if the mutation is causing a reduction in BMPR1B signalling, it may act on an inhibitor of follicle differentiation. Further research in this area will concentrate on the elucidation of the natural ligands for BMPR1B at different stages of follicle development and examine the effect of BMPR1B mutation on the downstream signalling cascade

© 2003 Society for Reproduction and Fertility

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