Bacterial lipopolysaccharide induces apoptosis in the trout ovary

BACKGROUND: In mammals it is well known that infections can lead to alterations in reproductive function. As part of the innate immune response, a number of cytokines and other immune factors is produced during bacterial infection or after treatment with lipopolysaccharide (LPS) and acts on the reproductive system. In fish, LPS can also induce an innate immune response but little is known about the activation of the immune system by LPS on reproduction in fish. Therefore, we conducted studies to examine the in vivo and in vitro effects of lipopolysaccharide (LPS) on the reproductive function of sexually mature female trout. METHODS: In saline- and LPS -injected brook trout, we measured the concentration of plasma steroids as well as the in vitro steroidogenic response (testosterone and 17alpha-hydroxyprogesterone) of ovarian follicles to luteinizing hormone (LH), the ability of 17alpha,20beta-dihydroxy-4-pregnen-3-one to induce germinal vesicle breakdown (GVBD) in vitro, and that of epinephrine to stimulate follicular contraction in vitro. We also examined the direct effects of LPS in vitro on steroid production, GVBD and contraction in brook trout ovarian follicles. The incidence of apoptosis was evaluated by TUNEL analysis. Furthermore, we examined the gene expression pattern in the ovary of saline- and LPS-injected rainbow trout by microarray analysis. RESULTS: LPS treatment in vivo did not affect plasma testosterone concentration or the basal in vitro production of steroids, although a small but significant potentiation of the effects of LH on testosterone production in vitro was observed in ovarian follicles from LPS-treated fish. In addition, LPS increased the plasma concentration of cortisol. LPS treatment in vitro did not affect the basal or LH-stimulated steroid production in brook trout ovarian follicles. In addition, we did not observe any effects of LPS in vivo or in vitro on GVBD or follicular contraction. Therefore, LPS did not appear to impair ovarian steroid production, oocyte final maturation or follicular contraction under the present experimental conditions. Interestingly, LPS administration in vivo induced apoptosis in follicular cells, an observation that correlated with changes in the expression of genes involved in apoptosis, as evidenced by microarray analysis. CONCLUSION: These results indicate that female trout are particularly resistant to an acute administration of LPS in terms of ovarian hormone responsiveness. However, LPS caused a marked increase in apoptosis in follicular cells, suggesting that the trout ovary could be sensitive to the pro-apoptotic effects of LPS-induced inflammatory cytokines

Gonad differentiation in zebrafish is regulated by the canonical Wnt signalling pathway

Zebrafish males undergo a ‘‘juvenile ovary-to-testis’’ gonadal transformation process. Several genes, including nuclear receptor subfamily 5, group A (nr5a) and anti-Mu¨ llerian hormone (amh), and pathways such as Tp53-mediated germ-cell apoptosis have been implicated in zebrafish testis formation. However, our knowledge of the regulation of this complex process is incomplete, and much remains to be investigated about the molecular pathways and network of genes that control it. Using a microarray-based analysis of transforming zebrafish male gonads, we demonstrated that their transcriptomes undergo transition from an ovary-like pattern to an ovotestis to a testislike profile. Microarray results also validated the previous histological and immunohistochemical observation that there is high variation in the duration and extent of commitment to the juvenile ovary phase among individuals. Interestingly, global gene expression profiling of diverging zebrafish juvenile ovaries and transforming ovotestes revealed that some members of the canonical Wnt/beta-catenin signaling pathway were differentially expressed between these two phases. To investigate whether Wnt/beta-catenin signaling plays a role in zebrafish gonad differentiation, we used the Tg (hsp70l:dkk1b-GFP)w32 line to inhibit Wnt/beta-catenin signaling during gonad differentiation. Activation of dkk1b-GFP expression by heat shock resulted in an increased proportion of males and corresponding decrease in gonadal aromatase gene (cyp19a1a) expression. The Wnt target gene, lymphocyte enhancer binding factor 1 (lef1), was also down-regulated in the process. Together, these results provide the first functional evidence that, similarly to mammals, Wnt/beta-catenin signaling is a ‘‘pro-female’’ pathway that regulates gonad differentiation in zebrafish.Web of Scienc

Advances in comparative endocrinology : vol. VIII

Ponències presentades al 10th Congress of the Iberian Association of Comparative Endocrinology (AIEC), celebrat a la Universitat Jaume I, els dies 23 al 25 de setembre de 2015Les diverses comunicacions presentades al 10è Congrés de la Asociación Ibérica de Endocrinología Comparada (23-25 setembre 2016, Castelló) s'agrupen en aquest volum. Les intervencions han aportat els darrers avenços en àrees científiques com ara reproducció, metabolisme, estrés, resposta immune, creixement, mineralització i pigmentació...Las diversas comunicaciones presentadas en el 10º Congreso de la Asociación Ibérica de Endocrinología Comparada (23-25 septiembre 2016, Castellón) se agrupan en este volumen. Las intervenciones han aportado los últimos adelantos en áreas científicas como por ejemplo reproducción, metabolismo, estrés, respuesta inmune, crecimiento, mineralización y pigmentación...The present volume of Advances in Comparative Endocrinology collects the contributions of the participants at the 10th Congress of the Iberian Association of Comparative Endocrinology (AIEC). Eighteen years after the foundational meeting of our Association in Peñíscola, the return of this Congress to Castellón highlights the growing success of this initiative to foster the research and scientific development in the field of comparative endocrinology developed in the Iberian Peninsula. AIEC meetings have proven to be a way to keep in contact among research groups with common interests. Some of the participants in this last meeting were also present in the foundational one, others members came after and keep assisting every time. As one of the aims of AIEC has been to encourage students to participate, we are particulary proud of those young students and doctors from the first editions that have gained more permanent positions and continue participating in the AIEC meetings with new students

Aging of Xenopus tropicalis Eggs Leads to Deadenylation of a Specific Set of Maternal mRNAs and Loss of Developmental Potential

As first shown more than 100 years ago, fertilization of an aged (overripe) egg increases the rate of malformations and embryonic loss in several vertebrates, including possibly humans as well. Since the molecular events in aging eggs may be similar in these species, we established in the frog Xenopus tropicalis a defined protocol for delayed fertilization of eggs. A three-hour delayed fertilization led to a dramatic increase in malformation and mortality. Gene expression profiling revealed that 14% of the polyadenylated maternal transcripts were downregulated upon aging. These transcripts were not degraded, but rather deadenylated as shown for specific maternal mRNAs. The affected transcripts are characterized by a relatively short 3′UTR and a paucity of cytoplasmic polyadenylation elements (CPE) and polyadenylation signals (PAS). Furthermore, maternal mRNAs known to be deadenylated during egg maturation as well as after fertilization were preferentially deadenylated in aged eggs. Taken together our analysis of aging eggs reveals that unfertilized eggs are in a dynamic state that was previously not realized. On the one hand deadenylation of transcripts that are typically deadenylated during egg maturation continues and this implies overripeness of the aged egg in the truest sense of the word. On the other hand transcripts that normally are deadenylated after fertilization loose their poly(A) in the aged egg and this implies that the egg awaiting fertilization starts processes that are normally only observed after fertilization. Based on our novel finding we postulate that the imbalance of the polyadenylated maternal transcripts upon egg aging contributes to the loss of developmental potential. Based on this hypothesis the developmental consequences of downregulation of specific transcripts can be analyzed in future

Meta-analysis of microarray data of rainbow trout fry gonad differentiation modulated by ethynylestradiol

Sex differentiation in fish is a highly labile process easily reversed by the use of exogenous hormonal treatment and has led to environmental concerns since low doses of estrogenic molecules can adversely impact fish reproduction. The goal of this study was to identify pathways altered by treatment with ethynylestradiol (EE2) in developing fish and to find new target genes to be tested further for their possible role in male-to-female sex transdifferentiation. To this end, we have successfully adapted a previously developed bioinformatics workflow to a meta-analysis of two datasets studying sex reversal following exposure to EE2 in juvenile rainbow trout. The meta-analysis consisted of retrieving the intersection of the top gene lists generated for both datasets, performed at different levels of stringency. The intersecting gene lists, enriched in true positive differentially expressed genes (DEGs), were subjected to over-representation analysis (ORA) which allowed identifying several statistically significant enriched pathways altered by EE2 treatment and several new candidate pathways, such as progesterone-mediated oocyte maturation and PPAR signalling. Moreover, several relevant key genes potentially implicated in the early transdifferentiation process were selected. Altogether, the results show that EE2 has a great effect on gene expression in juvenile rainbow trout. The feminization process seems to result from the altered transcription of genes implicated in normal female gonad differentiation, resulting in expression similar to that observed in normal females (i.e. the repression of key testicular markers cyp17a1, cyp11b, tbx1), as well as from other genes (including transcription factors) that respond specifically to the EE2 treatment. The results also showed that the bioinformatics workflow can be applied to different types of microarray platforms and could be generalized to (eco)toxicogenomics studies for environmental risk assessment purposes

Maternal effects on oocyte quality in farmed Atlantic halibut (Hippoglossus hippoglossus L.)

Atlantic halibut (Hippoglossus hippoglossus) oocyte quality is highly variable and one of the major bottlenecks during fry-production for on-growth in commercial Atlantic halibut farming. In this study, the effect of maternally derived oocyte constituents (i.e. yolk components and mRNAs) on oocyte quality (i.e fertilisation, embryonic hatching and normal blastomere symmetry) in farmed Atlantic halibut has been investigated. Atlantic halibut embryos and larvae depend on nutritional yolk components until larval first feeding. The importance of yolk n-3 fatty acids for oocyte quality was confirmed. However, highest positive correlations with oocyte quality were found for the less studied fatty acids dihomo-γ-linolenic acid (DGLA, 20:3n6) and docosapentaenoic acid (DHA, 20:5n3) that are known to compete with two of the most abundant fatty acids, arachidonic acid (ARA, 20:4n6)and docosahexaenoic acid (DPA, 22:5n3), respectively during fatty acid metabolism. High methionine and aspartic concentrations, amino acids essential to eukaryotic protein synthesis, were found to influence oocyte quality positively while no significant correlations were found between oocyte folate concentrations and oocyte quality. Before activation of zygotic transcription, maternal mRNAs control cell divisions and embryonic patterning. Due to the limited available genomic information on Atlantic halibut maternal transcripts, an expressed sequence tag (EST) maternal library containing 2,341high quality ESTs was created by suppressive subtractive hybridization (SSH). The maternal library constitutes an EST pool to identify suitable Atlantic halibut reference genes and identify differentially expressed maternal genes in high and low quality Atlantic halibut oocytes. To perform reliable quantification of gene expression by qPCR, stable reference genes have to be used to normalize target gene expression. Tubb2/Actb and Tbb2/Fau were identified as the best two-gene normalization factors during Atlantic halibut embryonic and larval development. Either of these normalization factors can be used for future developmental gene expression studies in Atlantic halibut. Tubb2/Actb was further used as reference gene during this study. Poor embryonic hatching success was found to not be correlated with a general decrease in oocyte maternal transcript abundance but with low transcript levels of specific maternal transcripts by qPCR. The majority of genes showed either no or very minor correlations between their transcript levels and oocyte quality parameters (Fertilisation: 13-93 %, embryonic hatching: 1-94 %). However, maternal transcript levels of three genes, most likely involved in nuclear protein and mRNA transport, growth factor regulation, and embryonic patterning, correlated with oocyte quality. Further, a new Atlantic halibut 4x44k oligonucleotide microarray was constructed and used to identify 192 strictly maternal genes during Atlantic halibut embryonic development and 20 differentially expressed genes between high and low quality oocytes, involved in immune response, metabolism, RNA transcription, protein degradation, cell signalling and the cytoskeleton. Microarray validation confirmed its suitability for future gene expression studies during Atlantic halibut embryonic development. The identified maternal genes in this study can serve as a pool for future in-depth studies of embryonic gene expression to advance the knowledge of important developmental processes such as germ cell development, growth and immune response in Atlantic halibut. Some of these may serve as possible markers for Atlantic halibut oocyte quality due to their high expression differences between high and low quality oocytes. Future nutritional studies on Atlantic halibut broodstock should focus on the identified yolk constituents acting positively on oocyte quality

Study of genetic factors and temperature influence on sex determination and differentiation in turbot

Sex, as intuitive and simple as it may seem to us, poses some of the most interesting and complex questions when studying life. Sex is an intrinsic characteristic of most eukaryote species which eventually has led to the appearance of two differentiated adult phenotypes or sexes, males and females. This distinction rules a huge part of our lives and is the origin of important evolutionary processes based on intra-sex competition or inter-sex conflict due to sexual antagonism. Furthermore, sex is an important character for a plethora of species involved in human activities, for example in aquaculture many fish species present sex size dimorphisms where one sex grows faster than the other, and so knowing how sex is determined in each species is of the outmost interest. Traditionally, sex determination has been considered a cascade process with a master gene at the top, but recent findings have suggested that, instead, it might be a network process where different genetic and environmental factors can alter gonad fate, which in turn would be connected with a huge number of different sex determination mechanisms in vertebrates, especially in poikiloterms. In this new view of sex, the different players involved in sex differentiation gain relevance and their study may help us understanding how the fate of the gonad is determined. In this work, we have studied sex differentiation in turbot, a flatfish with a marked sex dimorphism where females grow faster than males. This species presents genetic sex determination, but also temperature effects on sex ratios have been reported, which seem to be family-dependant. Our aim was to study sex differentiation in turbot to gain knowledge about how sex is determined in this species and also in a broader sense in fish. This work consists of expression studies in turbot gonads using two different techniques: real-time PCR and microarrays. First of all, the real time PCR technique was setup for gonad development studies in turbot. The different methods available for reference gene stability calculation and efficiency determination were assessed. Then, using this information we performed an extensive expression study on turbot sex differentiation ranging from undifferentiated to differentiated gonads at three different temperatures. We found that the first molecular signs of sex differentiation are observed at 90 days post fertilization and that three genes, cyp19a1a, amh and vasa, can be used to sex turbot at this stage. Furthermore, the expression of genes involved in germ cell development pointed towards their involvement in early sex differentiation and possibly sex determination. Temperature effects on sex differentiation were also assessed in this study. A higher proportion of females was obtained at cold temperatures and several genes showed temperature dependant expression changes. Finally, to complete our study, we also performed a microarray analysis in turbot gonad samples from undifferentiated individuals to male and female juveniles. Female gonads were found to be more different from undifferentiated gonads than those of males, requiring the regulation of a large number of genes and the involvement of different processes including epigenetic mechanisms. Furthermore, the involvement of known sex differentiation genes and previously unrelated genes in sex differentiation was observed. This study has widened our knowledge on sex differentiation in turbot in particular and in fish in general, helping to understand the role of many genes involved in sex differentiation across the whole vertebrate taxa and pointing towards other genes which have been connected with sex for the first time. Our data suggest that a network model might be more accurate to explain sex determination in turbot, where the environment can interact with genetic factors and modify gonad fate

Photoperiod regulation of molecular clocks and seasonal physiology in the Atlantic salmon (Salmo salar)

Recent years have seen considerable advances in the study of biological rhythms and the underlying molecular mechanisms that drive the daily and seasonal physiology of vertebrates. Amongst teleosts the majority of work in this field has focused on the model species the zebrafish to characterise clock genes and the molecular feedback loop that underpins circadian rhythms and physiology. Daily profiles of clock gene expression in a wide variety of tissues and cell types are now relatively well described. However the zebrafish is a tropical species that does not display distinct seasonality and therefore may not be the species of choice to investigate the entrainment of circannual physiology. In contrast, Atlantic salmon is a highly seasonal teleost that displays considerable temporal organisation of most physiological processes. In salmonids photoperiod is widely known to synchronise physiology to the environmental conditions and as such photoperiod manipulation is routinely used by the salmon industry throughout the production cycle to control and manipulate spawning, smoltification and puberty. Previous studies in salmonid species have already identified a set of clock genes that are linked to these seasonal physiological processes. However, to date, the molecular mechanisms regulating daily and seasonal physiology are largely unknown despite the strong commercial relevance in the Atlantic salmon. In the Atlantic salmon, Davie et al (2009) was the first to report the photoperiod dependent circadian expression of clock genes (Clock, Bmal and Per2 and Cry2) in the brain of the Atlantic salmon. In the same investigation the expression of clock genes was reported in a wide variety of peripheral tissues, however 24h profiles of expression in peripheral tissues were not characterised. In order to examine further the role of seasonal photoperiod on the circadian expression of clock genes, the present work first aimed to characterise diel profiles of Clock, Per1 and Per 2 expression in the brain together with plasma melatonin levels in II Atlantic salmon acclimated to either long day (LD), short day (SD), 12L:12D (referred to as experiment 1 throughout) and SNP (referred to as experiment 2 throughout). Photoperiod dependent clocks were also investigated in peripheral tissues, namely in the fin and liver. Results showed circadian profiles of melatonin under all photoperiods. In experiment 1 both Clock and Per2 displayed significant circadian expression in fish exposed to LD. This is in contrast to previous results where rhythmic clock gene expression was observed under SD. In addition, clock gene expression differed in response to experimental photoperiod in the liver, and diel rhythm differed to that of the brain. No rhythmic expression was observed in the fin. Levels of plasma melatonin exhibited a circadian rhythm peaking during the nocturnal phase as expected. However the amplitude of nocturnal melatonin was significantly elevated under LD (experiment 1) and the SNP long day photoperiod and 2010 autumnal equinox samples (experiment 2). Overall results from these experiments suggested that the control of clock gene expression would be photoperiod dependent in the brain and the liver however photoperiod history is also likely to influence clock gene expression. Interestingly, the gradual seasonal changes in photoperiod under SNP did not elicit similar profiles of clock gene expression as compared to experimental seasonal photoperiods and clock gene expression differed between experimental photoperiod and SNP treatments. In experiment 2 significant seasonal differences were also observed in the amplitude of individual clock gene expression. The mechanisms underlying this and potential impact on seasonal physiology are unknown. Developmental changes such as the smoltification process or abiotic factors such as temperature or salinity should be further investigated. In mammals previous work has focused on the molecular switch for photoperiod response and regulation of thyroid hormone bioactivity via deiodinase mediated conversion of T4 to the biologically active form T3. In mammals and birds expression of key seasonal molecular markers i.e. Tsh, Eya3 and Dio2, are up-regulated hours after exposure to the first LD and III persist under chronic LD conditions. In order to confirm the involvement of these genes in the seasonal photoperiodic response in salmon, a microarray study was first carried out. Results displayed transcriptome level differences in the seasonal expression of a wide variety of target genes including Eya3 and Dio1-3 in relation to LD and SD photoperiod suggesting that these genes may have a conserved role in salmon. qPCR validations of selected genes of interest were then performed (Dio1, Dio2 and Dio3, Eya3 and Tshover diel cycles in fish exposed to LD and SD photoperiod (autumn acclimated fish). In addition an unrelated qPCR study was undertaken in salmon parr acclimated to LD, 12L12D and SD photoperiod (spring acclimated fish)(Dio2, Eya3 and Tsh. Consistent with findings obtained in other vertebrate species, circadian expression of Dio2 was observed under LD. However expression of Eya3 and Tsh appeared to be dependent on photoperiod history prior to acclimation to the experimental photoperiods as already suggested for clock gene expression in this thesis. This is potentially a consequence of direct regulation by clock genes. To our knowledge, this is the first report on the expression of key molecular components that drive vertebrate seasonal rhythms in a salmonid species. The thesis then focused on another key component of the photoneuroendocrine axis in fish, the pineal organ. In the Atlantic salmon, as in other teleosts the photoreceptive pineal organ is considered by many to be essential to the generation, synchronisation and maintenance of circadian and seasonal rhythms. This would be primarily achieved via the action of melatonin although direct evidence is still lacking in fish. In salmonids the production of pineal melatonin is regulated directly by light and levels are continually elevated under constant darkness. In non salmonid teleosts the rhythmic high at night/ low during day melatonin levels persists endogenously under constant conditions and is hypothesised to be governed by light and intra- pineal clocks. The aims of the present in vitro and in vivo trials were to determine if circadian clocks and Aanat2 expression, the rate limiting enzyme for melatonin IV production, are present in salmon, test the ability of the pineal to independently re-entrain itself to a different photoperiod and establish whether the candidate clock genes and Aanat2 expression can be sustained under un-entrained conditions. Expression of clock genes was first studied in vitro with pineal organs exposed to either 12L:12D photoperiod, reversed 12D:12L photoperiod and 24D. Clock gene expression was also determined in vivo, in fish exposed to 12L:12D. Results were then contrasted with an in vitro (12L:12D) investigation in the European seabass, a species displaying endogenous melatonin synthesis. Results revealed no rhythmic clock gene (Clock, per1 and per2) expression in isolated salmon pineals in culture under any of the culture conditions. In the seabass, Clock and Per1 did not also display circadian expression in vitro. However rhythmic expression of Cry2 and Per1 was observed in vivo in the salmon pineal. This suggested some degree of extra-pineal regulation of clocks in the Atlantic salmon. In terms of Aanat2 no rhythmic expression was observed in the Atlantic salmon under any experimental conditions while rhythmic expression of Aanat2 mRNA was observed in seabass pineals. This is consistent with the hypothesis that in salmonids AANAT2 is regulated directly at the protein level by light while in other teleosts, such as seabass, AANAT2 is also regulated by clocks at a transcriptional level. Post hoc in silico analysis of the Aanat 2 5’ regulatory region revealed the absence of a functional E-box element in the salmon in comparison to other teleosts, including the European seabass, confirming the absence of clock regulation of Aanat2 mRNA in salmon. Although it is crucial to first characterise the molecular mechanisms regulating daily and seasonal rhythms, understanding how these mechanisms impact on the animal’s physiology is critical. One such aspect is the circadian regulation of fatty acid metabolism and cholesterol homeostasis ultimately impacting fat deposition in commercially produced Atlantic salmon. This is an area of considerable research interest both in terms of human health and improving the sustainability of commercial salmon feed. In mammals a number of genes involved in V liver lipid and cholesterol homeostasis are rhythmically expressed under the control of clock genes via Rev-erb . The aim of the present work was to determine diel mRNA expression patterns of selected genes involved in cholesterol homeostasis (Srebp 1, Srebp 2, Fas, Lxr, Elovl5, Hmgcr and D6 Fad) together with circadian clocks (Bmal1, Clock, Per 1, Per 2 and Rev-erb ) in the liver of the Atlantic salmon. Results demonstrated significant circadian expression of Srebp 1 and Bmal 1, similar to previous results in mice, Lxr also exhibited significant circadian expression. Additionally the gene coding for the rate limiting enzyme in cholesterol synthesis, Hmgcr, was significantly elevated during the day. This is in contrast to mammals where mRNA expression and protein activity was elevated during the night. Also in contrast to results obtained in mammals, Per1, Per2, Fas, and Reverb did not display significant circadian rhythmicity in salmon. This investigation represents the first attempt to correlate 24h profiles of clock gene expression to a functionally important process in peripheral tissues, lipid metabolism, which is an area of considerable interest for future research in this commercially important species. This thesis has significantly advanced knowledge on the expression of clock and seasonal genes in response to photoperiod information in the Atlantic salmon. Moreover it has given an important insight into the expression of clock genes in multiple tissue types and how clocks can regulate important physiological processes. However research is still in the early days and much work is needed to understand such a complex network in this highly seasonal and commercially important species

Expression profiling of rainbow trout testis development identifies evolutionary conserved genes involved in spermatogenesis.

Chantier qualité GAInternational audienceBACKGROUND: Spermatogenesis is a late developmental process that involves a coordinated expression program in germ cells and a permanent communication between the testicular somatic cells and the germ-line. Current knowledge regarding molecular factors driving male germ cell proliferation and differentiation in vertebrates is still limited and mainly based on existing data from rodents and human. Fish with a marked reproductive cycle and a germ cell development in synchronous cysts have proven to be choice models to study precise stages of the spermatogenetic development and the germ cell-somatic cell communication network. In this study we used 9K cDNA microarrays to investigate the expression profiles underlying testis maturation during the male reproductive cycle of the trout, Oncorhynchus mykiss. RESULTS: Using total testis samples at various developmental stages and isolated spermatogonia, spermatocytes and spermatids, 3379 differentially expressed trout cDNAs were identified and their gene activation or repression patterns throughout the reproductive cycle were reported. We also performed a tissue-profiling analysis and highlighted many genes for which expression signals were restricted to the testes or gonads from both sexes. The search for orthologous genes in genome-sequenced fish species and the use of their mammalian orthologs allowed us to provide accurate annotations for trout cDNAs. The analysis of the GeneOntology terms therefore validated and broadened our interpretation of expression clusters by highlighting enriched functions that are consistent with known sequential events during male gametogenesis. Furthermore, we compared expression profiles of trout and mouse orthologs and identified a complement of genes for which expression during spermatogenesis was maintained throughout evolution. CONCLUSION: A comprehensive study of gene expression and associated functions during testis maturation and germ cell differentiation in the rainbow trout is presented. The study identifies new pathways involved during spermatogonia self-renewal or rapid proliferation, meiosis and gamete differentiation, in fish and potentially in all vertebrates. It also provides the necessary basis to further investigate the hormonal and molecular networks that trigger puberty and annual testicular recrudescence in seasonally breeding species