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AgResearch, Wallaceville Animal Research Centre, PO Box 40063, Upper Hutt, New Zealand, 1 Teagasc, Athenry Research Centre, Athenry, Ireland,2 School of BMS, Oxford Brookes University, Gipsy Lane, Headington, Oxford X3 OBP, UK and 3 Biomedicum Helsinki, PO Box 63 (Haartmaninkatu 8), FIN-00014, University of Helsinki, Helsinki, Finland
Correspondence should be addressed to Ken P McNatty; Email: ken.mcnatty{at}agresearch.co.nz
Ovulation rate in mammals is determined by a complex exchange of hormonal signals between the pituitary gland and the ovary and by a localised exchange of hormones within ovarian follicles between the oocyte and its adjacent somatic cells. From examination of inherited patterns of ovulation rate in sheep, point mutations have been identified in two oocyte-expressed genes, BMP15 (GDF9B) and GDF9. Animals heterozygous for any of these mutations have higher ovulation rates (that is, + 0.8–3) than wild-type contemporaries, whereas those homozygous for each of these mutations are sterile with ovarian follicular development disrupted during the preantral growth stages. Both GDF9 and BMP15 proteins are present in follicular fluid, indicating that they are secreted products. In vitro studies show that granulosa and/or cumulus cells are an important target for both growth factors. Multiple immunisations of sheep with BMP15 or GDF9 peptide protein conjugates show that both growth factors are essential for normal follicular growth and the maturation of preovulatory follicles. Short-term (that is, primary and booster) immunisation with a GDF9 or BMP15 peptide-protein conjugate has been shown to enhance ovulation rate and lamb production. In summary, recent studies of genetic mutations in sheep highlight the importance of oocyte-secreted factors in regulating ovulation rate, and these discoveries may help to explain why some mammals have a predisposition to produce two or more offspring rather than one.
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