Submitted by Automa??o e Estat?stica (sst@bczm.ufrn.br) on 2015-12-14T22:12:12Z No. of bitstreams: 1 BarbaraPinheiroMaiaCavalcantiTadewald_DISSERT.pdf: 813424 bytes, checksum: f43cf35dc3635ca3f310dffda2d52c3f (MD5) / Approved for entry into archive by Arlan Eloi Leite Silva (eloihistoriador@yahoo.com.br) on 2015-12-18T20:47:16Z (GMT) No. of bitstreams: 1 BarbaraPinheiroMaiaCavalcantiTadewald_DISSERT.pdf: 813424 bytes, checksum: f43cf35dc3635ca3f310dffda2d52c3f (MD5) / Made available in DSpace on 2015-12-18T20:47:16Z (GMT). No. of bitstreams: 1 BarbaraPinheiroMaiaCavalcantiTadewald_DISSERT.pdf: 813424 bytes, checksum: f43cf35dc3635ca3f310dffda2d52c3f (MD5) Previous issue date: 2013-12-20 / Os esteroides sexuais influenciam o comportamento de vertebrados por meio de efeitos organizacionais e ativacionais. Estas a??es podem ocorrer em per?odos do desenvolvimento fetal, p?s-natal inicial e, ainda, durante a puberdade (efeito organizacional) ou alterando a express?o de padr?es comportamentais durante todas as fases da vida (efeito ativacional). Estudos sobre lateraliza??o no uso das m?os em primatas humanos e n?o humanos mostram que os horm?nios sexuais participam no processo de estabiliza??o da prefer?ncia manual que parece ocorrer a partir da puberdade e se mant?m na idade adulta. O objetivo deste estudo foi investigar emCallithrix jacchus machos adultos se a estabiliza??o da for?a da prefer?ncia manual, independentemente da dire??o (efeito organizacional), ? influenciada pela varia??o dos andr?genos (efeito ativacional). O uso preferencial de uma ds m?os foi estudado em 14animais em dois contextos: (1) uso espont?neo das m?os em pegar o alimento; (2) durante o uso for?ado de uma das m?os para alcan?ar o alimento com restri??o produzida pelo uso de anteparo com um orif?cio central que permitia o uso de apenas uma das m?os. Os registros foram realizados durante a fase basal em 5 sess?es/20 registros cada para as duas atividades na fase basal (n=100) e ap?s dois tratamentos: (a) uso de 100?g do antagonista do horm?nio liberador de gonadotrofinas (GnRH), Cetrotide - acetate of cetrorrelix (Baxter Oncology GmbH, Germany) (n=10) em dose ?nica, em 10 animais; (2) uso de 0,2 mg do GnRH (Sigma - Aldrich) (n= 8; 4 deles receberam o antagonista entre 6-8 meses antes), nos dias 1, 2, 7, 15 e 30 dias/20 registros em cada, totalizando 100 episodes para cada contexto ap?s os tratamentos. A partir destes registros foi calculado o ?ndice de lateraliza??o absoluto em rela??o apenas a for?a e o ?ndice do desvio de lateralidade para direita ou esquerda. A coleta de fezes para dosagem dos andr?genos fecais foi realizada durante os dias de coleta dos registros de uso da m?o na fase basal e ap?s os dois tratamentos. A an?lise estat?stica utilizou o modelo de efeitos mistos e o teste de Tukey para comparar as diferen?as entre as m?dias dos dois tratamentos, e o teste de Levene de vari?ncia das m?dias, todos para o p-valor de < 0,05. Na fase basal 6 animais usaram preferencialmente a m?o direita, 5 a esquerda e 3 se mostraram ambidestros. As m?dias dos ?ndices de lateraliza??o da fase basal diferiram daquelas ap?s os tratamentos, a partir do dia 7. A vari?ncia das m?dias dos ?ndices de lateraliza??o antes e ap?s a aplica??o dos tratamentos para a atividade espont?nea e a for?ada n?o apresentaram diferen?as significativas, mas o tratamento com o GnRH aumentou significativamente o ?ndice em rela??o ao tratamento com o seu antagonista. Estes resultados sugerem que os andr?genos possuem um efeito ativacional sobre a prefer?ncia manual em machos adultos de C. jacchus. / The role of steroids hormones on the behavior of vertebrates have been described as organizational and activational effects. These actions occur in different periods of the ontogenetic development as fetal, early post natal and during puberty (organizational effect) or modifying the expression of behavioral patterns during time life (activational effects). Studies on brain lateralization in hand use in human and non-human primates have shown that sexual hormones seems to participate in the process of handedness strength that begins in the puberal period and is stabilized at the adult age. The aim of this study was to investigate in adult male Callithrix jacchus if the strength of use of the hand in common marmoset adult male is stable (organizational effect) or androgens variations could affect its stability (activational effect). The preferential use of one hand in 14 common marmoset (Callithrix jacchus was studied in two contexts: (1) spontaneous holding food and directing the food to mouth (feeding episodes), and (2) forced reaching food tests where the animal have to reach the food through a hole within a cover plate with a central hole that allow the use of one hand only to reach the food. The records were made during 5 sessions/20 bouts each during baseline totalizing 100 episodes before two treatments. Firstly it was used GnRH antagonist: a single subcutaneous injection of 100?g de Cetrotide ? acetate of cetrorrelix (Baxter Oncology GmbH, Germany) (n=10). Secondly, a single GnRH injection of 0.2mg of GnRH (Sigma ? Aldrich) (n= 8) was used. After injections 20 successful attempts of hand use episodes was recorded in the 1st , 2 nd, 7th, 15th and 30 th days, totalizing in the whole period 100 episodes for each context, after both treatments. Fecal sampling to measure extracted fecal androgens was performed in all days of data collection across the length of the basal and during the experimental periods. Statistical analysis by mixed model, Tukey test to compare mean values after the two treatments, and Levene test to compare mean variance were used, all for p-value < 0.05. In basal phase 6 animals used preferentially the right hand, 5 the left and 3 were ambidextrous. Mean handedness index in basal phase were different from that after both treatment starting at 7th day. Mean variance of handedness index for spontaneous and forced activities does not differs before and after both treatments but the mean values for GnRH index were higher than that observed for its antagonist. These findings suggested that androgens have an activational effect on handedness in adult male C. jacchus

O objetivo, deste estudo foi investigar o comportamento dos hormônios esteróides 17β-Estradiol (E2), 17α-hidroxiprogesterona (17α-OHP), Testosterona (T) e 11-Ketotestosterona (11-KT), em piracanjuba Brycon orbignyanus de diferentes sexos e idades, na estação reprodutiva, e nas fêmeas submetidas à reprodução induzida. Os animais utilizados no trabalho, eram criados em piscicultura comercial, mantidos em 3 viveiros, separados por lotes de diferentes idades. A coleta dos animais, consistiu de quatro machos e cinco fêmeas (48 meses), identificados através do dimorfismo sexual da espécie, e as demais idades, (12 e 24 meses), coletaram-se, 20 peixes de cada idade, para identificação do sexo através de histologia. Já o experimento de caracterização dos esteróides sexuais na reprodução induzida, foram coletadas cinco fêmeas, selecionadas através das características com: abdome abaulado, papila urogenital, saliente e avermelhada. Após captura, os peixes foram transportados ao laboratório, onde houve coleta de sangue, para quantificação do perfil plasmático de E2, 17α-OHP, T e 11-KT. Posteriormente, os animais foram abatidos e suas gônadas coletadas e fixadas, a fim de que fosse realizada análise histológica para identificação do sexo. Na reprodução induzida, foi coletado sangue em dois momentos: pré-indução (PI) e pós-extrusão (PE). O nível plasmático de E2 nos machos de 12 meses destaca sua ação no processo de proliferação e renovação das espermatogônia observado em machos imaturos. Nas fêmeas o E2 apresentou os maiores níveis (P<0,05) nos animais de 48 meses, confirmando assim, sua principal função na estimulação do processo de vitelogênese, e maturação final do oócito. Quanto aos andrógenos T e 11-KT, os maiores níveis (p<0,05) foram observados nos peixes adultos (48 meses), permitindo afirmar que estes atuam como feedback negativo, do FSH e feedback positivo do LH, fundamental no processo de maturação final e liberação dos gametas, além de regular o comportamento reprodutivo. O resultado da 17α-OHP, sugere que, nas idades estudadas, é indispensável por participar como precursor dos principais esteróides (T, E2 e 11-KT), além da 17α,20β dihydroxy-4-pregnen-3-one (17α,20β-DHP), essencial no estágio final de maturação, e desova na reprodução induzida. / The objective of this study was to investigate the physiological behavior of steroid hormones 17β-Estradiol (E2), 17α-hydroxyprogesterone (17α-OHP), testosterone (T) and 11-Ketotestosterone (11-KT) in Brycon orbignyanus with different sex and ages on the reproductive season and in females submitted to induced reproduction. The animals used in the study were kept in three ponds on a commercial fish farming, separated by lots with different ages. The sampling of animals consisted of the collection of four males and five females (48 months) identified by the sexual dimorphism of the specie. In the other groups (12 and 24 months), 20 fish of each age were collected for identification of sex through histology. In the experiment with characterization of the sexual steroids in the induced reproduction, were collected five females selected through the following characteristics: bulging abdomen and prominent reddish genital papilla. After capture, the fish were transported to the laboratory, where blood was collected for quantification of the plasma profile of E2, 17α-OHP, T and 11-KT Subsequently, the animals were slaughtered and their gonads were collected and fixed for histological analysis. In the induced females, blood was collected at two moments: pre-induction (PI) and post-extrusion (PE). The plasma profile of E2 is fundamental in immature males, highlighting its action in the process of proliferation and renewal of spermatogonia, observed in males of 12 months. In females E2 presented the highest levels (P <0.05) in animals at 48 months, thus confirming its main function in the stimulation of the vitellogenesis process and final oocyte maturation. The highest levels (p <0.05) of T and 11-KT androgens were observed in adult fish (48 months), allowing to affirm that they are acting as FSH negative feedback and LH positive feedback, fundamental in the final maturation and release of the gametes, besides regulating the reproductive behavior of the fish. The results of 17α-OHP suggest this hormon is fundamental in the studied ages because it is a precursor of the main steroids (T, E2 and 11-KT) and 17α, 20β-dihydroxy-4-pregnen-3-one (17α, 20β-DHP), essential in the final stage of maturation and spawning in induced reproduction.

Hormonally induced artificial propagation of individually marked broodstock was performed identically at two sequential reproductive seasons. In both years, four separate groups of females were intraperitonealy injected by carp pituitary extrakt, Supergestran (containing GnRH analogue Lecirelin), Ovopel and Dagin (containing GnRH analogue and dopamine inhibitor) at 21 °C. In control group, no injection was carried out in broodstock. It observed the effect of treatment on the ovulation ratio, survival and growth of broodfisch, the ability of stripping in the next season and the effect on eggs.

Die GABA-ergen Neurone als Teil des GnRH-Netzwerkes spielen eine Rolle bei den Veränderungen der altersabhängigen Prozesse der Reproduktionsfunktion. Um die Regulation der gonadalen Steroide auf die Expression von GAD in reproduktionsabhängigen Regionen zu untersuchen, wurde im ersten Teil der vorliegenden Arbeit das männliche Rattenmodell gewählt. Nach der Untersuchung des endokrinen Zustands der Tiere anhand der Radioimmunoassay-Methode (RIA) wurden die zellulären Gentranskripte der beiden Isoformen von GAD, GAD65 und GAD67, mittels der Methode der in situ Hybridisierung in der POA, im Nukleus suprachiasmaticus (SCN), im mediobasalen Hypothalamus (MBH) und im Gyrus dentatus bestimmt. In allen untersuchten Regionen konnte nach der Kastration und einer anschließenden dreiwöchigen Erholungszeit kein Effekt beobachtet werden. Die Administration von Estradiol bewirkt in der POA eine signifikante Erhöhung der Expression von GAD65 und GAD67 um nahezu 40%. In den restlichen Regionen konnte dagegen kein Effekt gemessen werden. Die Testosteronbehandlung zeigte eine negative Wirkung auf die Regulation nur von GAD67: Eine 30%-ige Abnahme in der POA und eine 15%-ige im SCN. Im Gegensatz dazu trat im MBH und im Gyrus dentatus eine Verminderung der Expression nur bei GAD65 auf. Aus den hier vorgestellten Ergebnissen kann folgendes abgeleitet werden: Testosteron und Estradiol regulieren in unterschiedlicher Weise die Expression von GAD und so wiederum die inhibitorische Funktion von GABA. Da in der SCN, im MBH und im Gyrus dentatus im Gegensatz zu Estradiol eine Testosteron-Wirkung gemessen wurde, existiert eine eigene androgene Regulation von GAD. Weil die Estradiol-Zugabe eine Zunahme der Expression von GAD bewirkte und dieser Effekt von einer Abnahme der LH-Konzentration im Serum der betroffenen Tiergruppe begleitet wurde, ist die These bestätigt, dass GABA mit ihren inhibitorischen Funktionen zur Übermittlung der positiven Rückkopplung von Estradiol auf die LH-Freisetzung auf der Ebene der POA und nicht auf der Ebene der Axone agiert. Im Gegensatz zu Estradiol kann eine Progesteronbehandlung bei persistent östrischen Ratten einen LH-Peak auslösen und somit den Östrus-Zyklus wieder in Gang bringen. Aufgrund dieser Tatsache wurde im zweiten Teil der vorliegenden Arbeit ein Tiermodell zur Untersuchung der molekularbiologischen altersabhängigen Veränderungen entwickelt. Dabei wurden drei Monate alte proöstrische Ratten (Y) und 12 Monate alte persistent östrische Ratten (MA) benutzt. Die MA-Ratten wurden mit Progesteron behandelt. Sowohl die MA-Ratten als auch die Y-Ratten wurden um 13 Uhr und um 17 Uhr getötet. Eine unbehandelte MA-Gruppe, deren Tiere um 10 Uhr getötet wurden, diente hier als Kontrollgruppe. Anhand der LH-Messung der untersuchten Gruppen wurde ein Kontrollwert (5 ng/ml LH) für die positive Reaktion der Tiere auf Progesteron (responding animals) festgestellt. Es konnte bei 44% der persistent östrischen Ratten ein erhöhter LH-Spiegel erfolgreich wieder erreicht werden. In den Gruppen dieses Modells entstand eine Analogie zwischen den Gruppen der behandelten MA-13-Uhr und Y-13-Uhr Tiere sowie zwischen den responding animals und den Y-17 Uhr-Tieren. Um aussagekräftige statistische Veränderungen entlang der hypothalamo-hypophysio-ovariellen Achse in individuellen Tieren zu erhalten, wurde die Taqman®-PCR und die quantitative, kompetitive RT-PCR eingesetzt. Dabei wurden die folgenden Gene untersucht: ER α und ER β, GnRH, GnRH-R, GAD65 und GAD67, sowie FSH-β. In der POA, Hypophyse und im Ovar wurde altersabhängigen Genexpression beobachtet: Eine signifikante Abnahme der Expression von ER β sowohl in der Gruppe responding animals als auch in deren analoger Gruppe wurde in der POA (34 %), Hypophyse (44 %) und im Ovar (um die 30 %) gemessen. In der Hypophyse verzeichneten die mRNA-Transkripte von ER α bei der Gruppe der behandelten mittelalten Ratten der 13 Uhr-Gruppe eine Zunahme von 55% und bei der 13-Uhr-Gruppe der jungen Ratten einen Anstieg von 153 %. Ebenso nehmen die mRNA-Konzentrationen von FSH-β sowohl bei den responding animals als auch bei deren analoger Gruppe in gleichem Masse (ungefähr 300 %) zu. Da die Veränderungen der Expression von ER β, ER α und FSH-β bei den zwei analogen Gruppen auftritt, ist zu vermuten, dass diese Gene altersabhängig expremiert und an der Zyklusregulation ursächlich beteiligt sind. Die restlichen Gene zeigten entlang der Achse keine altersrelevanten Veränderungen. Da ER β-Expressionsveränderungen in der POA, in der Hypophyse und im Ovar gemessen wurden, konnte der wichtigste Schluss der hier vorgestellten Untersuchungen gezogen werden, dass nämlich ER β für den Erhalt des Zyklus essentiell sein kann. In diesem Teil der vorliegenden Arbeit wurde ein Tiermodell zur molekular biologischen Untersuchung der altersabhängigen Veränderungen mit sehr zufriedenstellender Ausbeute zur Wiederherstellung des Östrus-Zyklus (44%) erfolgreich entwickelt. Dieses Modell ermöglichte darüber hinaus die Untersuchung einer relativ hohen Anzahl an Genen entlang der hypothalamo-hypophysio-ovariellen Achse.

Master of Science / Department of Animal Sciences and Industry / Jeffrey S. Stevenson / A study was performed to determine the minimum effective dose of human chorionic gonadotropin (hCG) needed to induce ovulation of follicles in cattle (Exp. 1). Another study determined the effects of replacing the first injection of GnRH (d -7) with hCG or saline in a Resynch-Ovsynch protocol [injection of GnRH 7 d before and 48 h after PGF[subscript2alpha] before a resynchronized fixed-timed AI (TAI)] on pregnancy rates in cows diagnosed not pregnant and pregnancy survival in cows diagnosed pregnant (d 0; Exp. 2). A final study determined the ovulation potential of hCG compared with GnRH and saline (Exp. 3). In Exp. 1, ovaries of Holstein cows were mapped by using transrectal ultrasonography 7 d before pregnancy diagnosis. Cows were assigned to treatments of saline, 100 [Mu]g of GnRH, or 500, 1,000, 2,000, or 3,000 IU of hCG. Ovarian structures were monitored 7 d later and proportion of cows and follicles that ovulated were recorded. In Exp. 2, cows in 4 herds were assigned to treatments of 1,000 IU of hCG, 100 [Mu]g of GnRH, or left as untreated controls 7 d before pregnancy diagnosis. Nonpregnant cows were given PGF[subscript2alpha] (d 0), then inseminated 72 h later, concurrent with a GnRH injection. Pregnancy rates tended (P = 0.08) to be increased by GnRH (17.9%; n = 703) compared with control (12.9%; n = 505), but not hCG (16.5%; n = 541). Incidences of ovulation in nonpregnant cows (Exp. 3) were: hCG (51.6%; n = 126), GnRH (46.1%; n = 102), and control (28.1%; n = 96), whereas those in pregnant cows were: hCG (59.3%; n = 59), GnRH (24.5%; n = 49), and control (6.9%; n = 58). We concluded that: 1) a minimum dose of 1,000 IU of hCG resulted in a greater ovulatory response than saline, GnRH, or 500 IU of hCG (Exp. 1); 2) initiating a Resynch-Ovsynch protocol 7 d before pregnancy diagnosis with saline reduced timed AI pregnancy rates (Exp. 2); and 3) incidence of new CL was greater after hCG than GnRH in pregnant cows, but not in nonpregnant cows (Exp. 3).

The plasma membrane electrical activities of neurons that secrete gonadotropin releasing hormone (GnRH), referred to as GnRH neurons hereafter, have been studied extensively. A couple of mathematical models have been developed previously to explain different aspects of these activities including spontaneous spiking and responses to stimuli such as current injections, GnRH, thapsigargin (Tg) and apamin. The goal of this paper is to develop one single, minimal model that accounts for the experimental results reproduced by previously existing models and results that were not accounted for by these models. The latter includes two types of membrane potential bursting mechanisms and the associated calcium oscillations in the cytosol. One of them has not been reported in experimental literatures on GnRH neurons and is thus regarded as a model prediction. Other improvements achieved in this model include the incorporation of a more detailed description of calcium dynamics in a three dimensional cell body with the ion channels evenly distributed on the cell surface. Although the model is mainly based on data collected in cultured GnRH cell lines, we show that it is capable of explaining some properties of GnRH neurons observed in several of other preparations including mature GnRH neurons in hypothalamic slices. One potential explanation is suggested. A phenomenological reduction of this model into a simplified form is presented. The simplified model will facilitate the study of the roles of plasma membrane electrical activities on the pulsatile release of GnRH by these neurons when it is coupled with a model of pulsatile GnRH release based on the autoregulation mechanism. / Science, Faculty of / Mathematics, Department of / Graduate

Sendo o GnRH a molécula capaz de iniciar a cascata hormonal reprodutiva, realizamos a clonagem, analisamos os efeitos da indução à reprodução e as funções dos GnRHs de A. altiparanae. Como resultados, obtivemos as sequências dos cDNAs do GnRH2 e GnRH3. Quando induzidos à reprodução, a desova foi às 20 h pós-estímulo (hpe) em fêmeas e às 16 hpe em machos, o aumento da expressão do mRNA de GnRH3 ocorreu às 8 hpe em fêmeas, e o aumento da expressão do mRNA de GnRH2 foi às 0 hpe em machos. Com relação ao efeito dos GnRHs, todos estimularam a expressão do mRNA de &beta;LH, mas não de &beta;FSH, e só o GnRH2 foi capaz de elevar o MIS e causar a desova. Como conclusão, temos que as sequências dos cDNAs dos GnRHs se mostraram conservadas; a indução à reprodução por redução do nível da água foi eficaz; em cativeiro, a espécie teve desenvolvimento assincrônico; o GnRH2 provavelmente está ligado ao comportamento reprodutivo, e o GnRH3 é a possível forma hipofisiotrópica. Por fim, só o GnRH2 desencadeou toda a cascata hormonal. / The study on reproduction in fish has been acquired great importance in last years, mainly for the benefit of threatened species. During the reproductive process, the hypothalamic neurons synthesize and release GnRH that stimulates the pituitary cells to release FSH and LH, which, in turn, promote the gonadal maturation. In fact, the morphological changes in gonads are the result of the endocrine action of the reproductive axis, in which the GnRH is the key molecule to starting the reproductive axis control. Thus, the knowledge about the GnRH, as well as about the gonadal morphological changes in the spawning might contribute to effectiveness of reproduction. Therefore, in this work, with Astyanax altiparanae as a model, we made the molecular characterization of the GnRHs, and we analyzed the gonadal morphological changes during the reproductive stimulus. In addition, we evaluated the role of injected GnRHs in vivo. As results, we obtain the cDNA complete sequence of preproGnRH2 (612bp) and preproGnRH3 (407bp) of A. altiparanae. Regarding the induction of reproduction by water level drawdown, the released of gametes occurred at 20 hours after stimulus in female and at 16 hours after stimulus in males, the mRNA expression of GnRH3 increased at 8 hours after stimulus in female and the mRNA expression of GnRH2 increased at 0 hours in males. Regarding the effects of injected GnRH, all of them stimulated the &beta;LH but not &beta;FSH mRNA expression, and only the GnRH2 was able to rise the MIS and stimulate the released of gametes. We conclude that the cDNAs sequences of preproGnRH2 and preproGnRH3 were conserved, although there is a change in the amino acid at the position 8 of the GnRH3 decapeptide of A. altiparanae. Furthermore, the induced reproduction by water level drawdown was effective, and in captivity, the A. altiparanae has an asynchronous development with splitted spawning during the breeding season. The analysis of the animals submitted to the reproductive stimulus allowed us to suggest that in A. altiparanae, the GnRH2 probably has a role in sexual behavior and the GnRH3 possibly is the hypophysiotropic form. Finally, analyzing the GnRH effects, we observed that only the GnRH2 was able to start the entire reproductive hormonal cascade, leading the animal to spawning.

BACKGROUND: Pleiotropy is a biological phenomenon of a single gene exhibiting influence over several different seemingly disparate phenotypes. This phenomenon poses significant challenges to fully understanding the etiologies of many different Mendelian diseases. Two such Mendelian diseases are Idiopathic Hypogonadotropic Hypogonadism (IHH) and Craniosynostosis (CS). IHH results from the failure of differentiation, migration, secretion, or action of the GnRH neurons resulting in absent puberty and infertility. CS is characterized by premature fusion of one or more of the cranial sutures resulting in dysmorphic shape of the skull that can lead to life-threatening raised intercranial pressure requiring surgical intervention. Thus far, 77 genes have been implicated in IHH and 128 genes have been implicated CS, both representing ~50% of the cases in their respective diseases. Recent research has suggested a shared molecular landscape in CS and IHH but the full ensemble of this overlap is not known. OBJECTIVE: This study will attempt to utilize human genetics, bioinformatics, statistics, phenotype data of IHH patients, and the prior literature in order to ascertain the full extent of the shared biology of IHH and CS. METHODS: The gene sets of both IHH and CS were used in gene overlap statistical analysis to investigate shared genetics. Whole exome sequencing data from 1,395 patients from the IHH cohort of the Massachusetts General Hospital were used for gene-variant burden analysis to determine genetic overlap with CS. Detailed physician notes from this cohort were used to determine phenotypic presence of CS in IHH. Conversely, evidence of reproductive phenotypes in genetically characterized CS patients was gathered from the reported CS gene literature. The CS and IHH gene sets were also bioinformatically analyzed using both the Metascape and DAVID bioinformatic platforms for pathway annotation, protein-protein interaction (PPI), and functional interactions to provide evidence for the mechanism of shared biology. RESULTS: Of the 128 CS genes and 77 IHH genes, 4 were determined to be causal for both diseases with a further 3 considered as potentially causal candidates for both diseases. The 4 overlapping causal genes were tested using three different methods and this overlap was determined to be of statistical significance (p<0.05). Furthermore, the phenotypic review revealed that while there was not a significant enrichment for CS phenotypes in the IHH cohort, the literature review yielded 49 of 128 CS genes that were reported with phenotypic evidence of failure of the hypothalamic-pituitary portion of the HPG axis. Gene-variant burden analysis yielded nominal (p<0.05) enrichment in the IHH cohort for 17 CS genes, of which 3 were significant after Bonferroni multiple testing correction (p<0.00039). The CS/IHH gene sets were both enriched in 44 shared pathways according to Metascape and 17 shared pathways according to DAVID. PPI analysis yielded 3 shared communities between the two disorders with enrichment in fibroblast signaling, ossification, and cardiac chamber development. CONCLUSIONS: The shared biology between IHH and CS was significantly greater than what was previously appreciated. Shared pathways of the two gene sets point toward the neural crest origin of subpopulations of the GnRH neuron and cranial suture osteoblast as a possible foundation for this shared biology, as well as the migratory nature of these two cells and the role that many genes in both gene sets play in cellular motility. Several CS genes emerge as candidates for IHH and must be individually evaluated. Functional studies should be used to confirm and further unravel the underlying mechanisms for the biological overlap between these two diseases. This study may provide a model for preemptive in silico work prior to more expensive in vitro or in vivo studies of pleiotropy.

L’apparition de la puberté et la régulation de la fertilité chez les mammifères sont contrôlées par un réseau neuronal complexe, situé principalement dans l'hypothalamus, et qui converge vers les neurones synthétisant l'hormone de libération des gonadotrophines (GnRH). Ces neurones régulent la sécrétion des gonadotrophines, la croissance et le fonctionnement des gonades. Le développement correct du système à GnRH, incluant des changements rapides dans l'expression et la signalisation de l’hormone GnRH au sein de cette population clairsemée de quelques centaines de neurones, est essentiel pour la maturation sexuelle et le fonctionnement normal de l'axe hypothalamo-hypophyso-gonadique. Lors du développement embryonnaire, ces neurones migrent de la placode olfactive vers leur emplacement définitif, l’hypothalamus, pour y recevoir les connexions afférentes qui permettront une libération pulsatile de la GnRH et la libération subséquente des gonadotrophines (l'hormone de stimulation des follicules (FSH) et l'hormone lutéinisante (LH)). Dès les années 90, l'oxyde nitrique (NO) a été identifié comme molécule clé dans la décharge pré-ovulatoire de GnRH/LH. En effet, de nombreux travaux ont suggéré que des interactions entre les neurones exprimant la forme neuronale de l’enzyme de synthèse du NO (la nNOS) et le système GnRH étaient impliquées dans le contrôle central de la fonction de reproduction à l'âge adulte. De plus, si le NO est reconnu depuis longtemps comme un acteur majeur du contrôle central de l’ovulation à l’âge adulte, la possibilité qu’il soit aussi impliqué dans la maturation sexuelle en régulant l’activité des neurones à GnRH à des stades précoces précédant la puberté n’a pas été explorée auparavant. Cependant, même si nous avons progressé dans la connaissance des interactions entre les neurones à nNOS et des différents acteurs importants de l’axe gonadotrope, l’identité moléculaire de ces neurones reste mal connue. Au cours de cette étude, nous avons recherché 1) l'identité moléculaire des neurones á nNOS dans l'hypothalamus au cours de développement 2) si le NO régule la migration et l’intégration des neurones à GnRH dans l’hypothalamus et 3) si le NO régule la maturation sexuelle. Pendant ma thèse nous avons répertorié pour la première fois les différents neurotransmetteurs et les principaux récepteurs dans les neurones à nNOS au cours du développement post-natal. De plus, les résultats de ma thèse montrent pour la première fois une implication de la signalisation du NO dans la migration des neurones à GnRH vers l'hypothalamus et font échos à l'identification d'une série de mutations de la NOS1 chez des patients atteints du syndrome de Kallmann, une maladie génétique congénitale rare qui associe une carence en GnRH, due à un défaut de migration neuronale, et une anosmie. Enfin, mes travaux montrent que le NO est un nouveau protagoniste dans la maturation post-natale du système à GnRH, la survenue de la puberté et l’acquisition de la capacité à se reproduire. Plus généralement, les résultats de ce travail de thèse permettent d’identifier de nouveaux mécanismes potentiellement responsables de troubles développementaux dans la mise en place des circuits neuronaux contrôlant l’axe gonadotrope chez les mammifères en général et l’homme en particulier. Nous espérons que ces résultats élargiront notre compréhension de la régulation de l'axe reproducteur, offrant ainsi des possibilités nouvelles de stratégies thérapeutiques contre les troubles de la fertilité. / The onset of puberty and the regulation of fertility in mammals are governed by a complex neural network, primarily in the hypothalamus, that converges onto gonadotropin-releasing hormone (GnRH)-producing neurons, the master regulators of gonadotropin secretion and postnatal gonadal growth and function. The proper development of the GnRH system, including timely changes in GnRH expression and signaling by this sparse population of a few hundred neurons, is essential for sexual maturation and the normal functioning of the hypothalamic-pituitary-gonadal axis. As the brain develops during embryogenesis, these neurons should move from the olfactory placode into the correct brain location in adequate numbers, and then establish the afferent connections that will allow the pulsatile release of GnRH peptide, and the subsequent release of the gonadotropins (follicle stimulating hormone, i.e FSH and luteinizing hormone, ie. LH). As early as in the 90’s NO was presented as a key molecule in the preovulatory GnRH/LH surge, and results from different groups, have suggested the interaction of NOS-containing neurons with the GnRH system, and their involvement in the regulation of reproductive capacity. Even though nitric oxide has now been long recognized as a key player in the central hormonal regulation of ovulation during adulthood, no one has considered the possibility that it could act in an earlier stage as the master regulator of GnRH neurons before puberty, hence participating in the actual maturation of the neuroendocrine axis. The relationship of nNOS-expressing neurons with other important molecules of the hypothalamic axis has been well studied, whilst the molecular identity of this neuronal NOS-expressing population is poorly documented. . To this end, we address the hitherto unaddressed questions concerning 1) the molecular identity of nNOS-expressing neurons in the developing hypothalamus, 2) the putative involvement of the NO molecule in the migration of GnRH neurons and the proper establishment of their afferent connections in the hypothalamic region and 3) the plausible determinant role of NO signaling in the maturation of the reproductive system. During this study we identified for the first time the cohort of the principal neurotransmitters and important receptors expressed by these cells in the hypothalamic region during development. Additionally, our results reveal for the first time an involvement of NO signaling in the migration of GnRH neurons in the hypothalamus and are in line with the identification of a series of NOS1 mutations in Kallmann syndrome (KS), a rare congenital genetic condition presenting a unique combination of GnRH deficiency, arising from a faulty migration of the neuronal population, and anosmia. Lastly, our study identifies NO as a novel protagonist during postnatal development, in the regulation of the onset of puberty and the acquisition of reproductive competence. Overall, the results of my Phd thesis identify putative new targets causing alterations of developmental programming under pathophysiological gestational environment in mammals in general, and in humans in particular. Here we thus provide new insights into the mechanisms by which the alteration of GnRH neuronal function leads to hypogonadotropic hypogonadism and infertility. We are hopeful that our results will expand our understanding of how the neuroendocrine axis is regulated and will possibly provide opportunities for therapeutic strategies against debilitating conditions.

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