No description available.

No description available.

No description available.

No description available.

No description available.

Sexually reproducing eukaryotes are typically going through a biphasic life cycle with a diploid and a haploid phase. Unlike in plants where selection on haploid pollen genotypes is well established, the possibility of selection occurring in animal sperm is currently not known. One of the main reasons for this lack of knowledge is the general assumption that due to the shortness and the apparent absence of gene expression in haploid sperm, selection during that phase is unlikely to occur. The aim of this thesis was to fill this gap and address some of the main fundamental questions. I investigated the interaction between sperm phenotype and offspring phenotype with a focus on the trans-generational effects of (i) selection on the haploid sperm genotype, (ii) sperm ageing and (iii) sperm-mediated epigenetic effects. For one, we performed several experimental studies to investigate how selection on the sperm phenotype affects offspring performance in two externally fertilizing fishes, Atlantic salmon and zebrafish. We found that in Atlantic salmon, sperm of intermediate post-activation longevity sire offspring that hatch earlier. In zebrafish, longer living sperm sire more viable offspring with a higher fitness than their short-lived sibling sperm. We explored the mechanisms of these trans-generational effects and found that neither intrinsic post-ejaculation sperm ageing (Atlantic salmon and zebrafish) nor pre-ejaculation sperm ageing (zebrafish) affect offspring performance. However, we identified genetic differences between sperm pools that were obtained by selecting different phenotypes within ejaculates of zebrafish males. These results suggest a genetic basis for intra-ejaculate sperm phenotype variation and show that there is potential for haploid selection in sperm. In a separate experiment, we explored the role of sexual selection in shaping sperm-mediated epigenetic effects, and found that short-time changes in male-male competition affect offspring hatching time and survival. In conclusion, this thesis provides evidence that sperm phenotype affects offspring phenotype, and that sperm phenotype is affected by both epigenetic changes influenced by the male environment and differences in the haploid genome of sperm.

Testicular function is fundamental to male fertility, since testicular cells act in collaboration with each other to signal sex differentiation, the initiation of puberty and spermatogenesis. Complications that can be influenced by many factors will affect sperm number, morphology, motility, chromatin quality and acrosomal integrity. The purpose of these studies was to analyze the changes in gene expression in the developing testes and analyze the seasonal changes in gene products in sperm of mature bucks. In the first experiment, testes were harvested from five Alpine bucks at 0, 2, 4, 6, and 8 months of age. Northern and in situ hybridization indicated that the largest change in gene expression occurred during the first 4 months of goat testes development. Sex determining region Y-box 9 (SOX9) and Heat Shock protein A8 (HSPA8) peaked at 2 months of age, and were expressed in Sertoli cells and spermatogonium, respectively. At 4 months, expression of Stimulated by Retinoic Acid gene 8 (STRA8), Protamine1 (PRM1) and Outer Dense Fiber protein 2 (ODF2) was strongly up-regulated in early and maturing germ cells, respectively. In the second experiment, RNA from ejaculated spermatozoa collected from mature Alpine bucks in peak (October) and non-peak (April) breeding season were analyzed on a 4 x 44K Agilent bovine microarray. One thousand three hundred and eighteen gene products were differentially expressed 2-fold or more (p ≤ 0.05 ) was expressed in mature goat sperm collected October and April. To eliminate the likelihood of false positives, the cut off was set to fold change of 3 or more at p ≤ 0.01 which narrowed the list of genes to 50 transcripts. Real time PCR results confirmed the expression of Sperm Adhesion Molecule 1 (SPAM1) in April, and the expression of Glycerol kinase 2(GK2) and Myc Binding Protein 2 (MYCBP2) in October. Based on the results from both experiments, it can be concluded that: SOX9 and HSPA8 expression play an important role in tubular formation and germ cell maintenance; two months after SOX9 and HSPA8 expression, genes that are associated with spermatogenesis initiation and completion are upregulated; and validation of the seasonal changes in sperm mRNA levels may provide additional insight to testicular events as they relate to breeding and non-breeding season.

published_or_final_version / Obstetrics and Gynaecology / Master / Master of Philosophy

Diss. (sammanfattning) Uppsala : Univ., 2001. / Härtill 5 uppsatser.

Thesis (M. Phil.)--University of Hong Kong, 2000. / Includes bibliographical references (leaves 108-135).