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Differences in the reproductive potential of female broiler parent and layer fowl are related to differences in the recruitment of follicles to the preovulatory hierarchy. Broiler and laying hens were fed ad libitum or a restricted diet during rearing and ad libitum after sexual maturity. The sensitivity of thecal tissue, from ovarian follicles of different sizes, from layer and broiler fowl to stimulation by pregnant mares' serum gonadotrophin (PMSG) was determined to test the hypothesis that differences in egg production are associated with changes in the sensitivity of ovarian follicles to stimulation by gonadotrophin. The activity of ornithine decarboxylase 0.5–4 h after injection of 200 iu PMSG kg−1 body mass was assessed in thecal tissue from small white follicles 2–3 and 5–6 mm in diameter and in the smallest preovulatory yellow follicle. Basal activity was similar in layers and broiler breeders. PMSG-stimulated ornithine decarboxylase activity in follicles of 5–6 mm diameter was greater in broiler breeders than in layers. There was no difference between the lines in PMSG-stimulated ornithine decarboxylase activity in follicles of 2–3 mm diameter or in small yellow follicles. It was concluded that the low egg production and high prevalence of eggs with defective shells in broiler parents compared with layers may be related to the increased sensitivity of follicles to endogenous gonadotrophins at the critical stage of recruitment to the preovulatory hierarchy.
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Critical age, weight and body composition have been suggested as necessary correlates of sexual maturity. A genome scan to identify quantitative trait loci (QTL) for age and body weight at first egg (AFE and WFE) was conducted on 912 birds from an F2 broiler–layer cross using 106 microsatellite markers. Without a covariate, QTL for body WFE were detected on chromosomes 2, 4, 8, 27 and Z and a single QTL for AFE was detected on chromosome 2. With AFE as a covariate, additional QTL for body WFE were found on chromosomes 1 and 13, with abdominal fat pad as covariate a QTL for body WFE was found on chromosome 1. With body WFE as covariate, additional QTL for AFE were found on chromosomes 1, 3, 4, 13 and 27. The QTL generally acted additively and there was no evidence for epistasis. Consistent with the original line differences, broiler alleles had positive effects on body WFE and negative effects on AFE, whereas the phenotypic correlation between the two traits was positive. The mapped QTL for body WFE cumulatively accounted for almost half the body weight difference between the chicken lines at puberty. Overlapping QTL for body WFE and body weight to 9 weeks of age indicate that most QTL affecting growth rate also affect body WFE. The co-localisation of QTL for body weight, growth and sexual maturity suggests that body weight and growth rate are closely related to the attainment of sexual maturity and that the genetic determination of growth rate has correlated effects on puberty.
