Biological invasions pose a serious threat to biodiversity world-wide. Through various means, such as competition or predation, invaders can radically change species composition and the functioning of native ecosystems. Even though our understanding of the mechanisms underlying invasion success is improving, there is still a lack of knowledge on the response of native species under pressure from invasion. This study adds to existing knowledge on the responses of a native species to invasion by non-indigenous species. Pyura pachydermatina is a native ascidian in the southeast coast of New Zealand currently under pressure from increased urbanisation and invasion by other ascidian species. The reproductive strategies employed by P. pachydermatina are investigated and the role of these strategies to increase its resistance to invasion are assessed. A population study on the status of P. pachydermatina around the Banks Peninsula was carried out in Camp Bay, Pigeon Bay, and Wainui. Spawning experiments using P. pachydermatina and gonad histology were done regularly during the one year study period to assess its ability to self-fertilise and determine its reproductive period. In addition, predation experiments were carried out to assess the susceptibility of P. pachydermatina early life stages to two amphipod predators. The surveys indicated that the populations of P. pachydermatina in the three sites are different from one another. Wainui has on average the largest individuals of P. pachydermatina and Camp Bay, the smallest. Abundance of P. pachydermatina was highest in Pigeon Bay and lowest in Wainui. The three life stages of Pyura pachydermatina; recruits, juveniles, and adults, were present in all sites at all seasons. The spawning experiments confirmed the species’ ability to self-fertilise and that it has a year-round spawning period. The two amphipod predators, Jassa marmorata and Caprella mutica, were efficient in consuming the egg and larval stages of P. pachydermatina, but did not feed on the settlers. Year-round reproduction and the ability to self-fertilise potentially give P. pachydermatina increased resistance to the effects of urbanisation and invasion. This population study suggested that the species is thriving around the Banks Peninsula. This, combined with previous studies on the non-indigenous ascidian Styela clava that stated the static or declining populations of the potential invaders, gives a positive outlook for the native species for the future. I suggest the use of genetic techniques to assess, in more detail, the population structure and dispersal potential of this native species. I also suggest constant monitoring of native species is required to keep up to date with the current status of the species, which will in turn help management decisions should regional spread of the Lyttelton S. clava invasion occur in the future.

Durant ma thèse, j’ai participé à une étude fonctionnelle qui a démontré que p120-RasGAP, une protéine appartenant à la famille GAP (GTPase-activating protein), est le médiateur cytoplasmique de l’éphrine lors de l’atténuation d’ERK1/2. Pour confirmer cela, j’ai réalisé une expérience de co-immunoprécipitation et j’ai démontré que p120-RasGAP s’associe au récepteur de l’éphrine, Eph3, quand celui-ci est activé par un ligand éphrine. Ce résultat indique fortement que les signaux FGF et éphrine convergent au niveau de Ras et qu’ils contrôlent de manière antagoniste son activité. Dès lors, j’ai analysé les autres événements de spécification cellulaire impliquant l’antagonisme FGF/éphrine. Chez l’embryon d’ascidie, le signal FGF est décrit comme inducteur du destin neural dans les cellules ectodermiques qui, en absence du signal FGF, adoptent le destin épidermique. L’induction neurale des ascidies a lieu au stade 32 cellules et se traduit par la spécification de quatre précurseurs neuraux (ERK+) parmi les 16 cellules ectodermiques. J’ai démontré que le signal éphrine/Eph/RasGAP antagonise le signal FGF pour générer une activation d’ERK1/2 de type tout ou rien parmi les cellules ectodermiques. Enfin, en collaboration avec Philip Abitua, doctorant dans le laboratoire du Dr. Mike Levine (UC Berkeley), nous démontrons que l’antagonisme entre les signaux éphrine et FGF est impliqué dans la régionalisation antéro-postérieure de la plaque neurale / During my thesis study, I was involved in functional studies to demonstrate that p120-RasGAP, a GTPase-activating-protein (GAP), is a cytoplasmic mediator of the ephrin-mediated ERK attenuation. To confirm this notion, I conducted a co-immunoprecipitation experiment and demonstrated that p120-RasGAP associates with an ephrin receptor, Eph3, when the latter is activated by an ephrin ligand in ascidian embryos. These results strongly indicate that FGF and ephrin signals converge at the level of Ras and control its activity antagonistically. Following this finding, I looked for other cell fate specification events controlled by the antagonism between ephrin and FGF signals. In ascidian embryos, FGF signals are known to induce neural fates in ectodermal cells which otherwise adopt epidermal fates. Ascidian neural induction takes place at the 32-cell stage, resulting in specification of specific four cells as ERK1/2-active neural precursors among 16 ectodermal cells. I was able to demonstrate that ephrin/Eph/RasGAP signals counterbalance FGF neural inducing signals to generate the ON-OFF response of ERK activation among the ectodermal cells. Finally, in collaboration with a PhD student in Dr. Mike Levine’s lab (UC Berkeley), the antagonism between ephrin and FGF signals plays a role in regionalisation of the neural plate along the anterior-posterior axis.

Les embryons d'ascidies se développent avec un lignage cellulaire stéréotypé et évolutionairement conservé pour produire en quelques heures ou jours un têtard comportant un petit nombre de cellules. De ce fait, ils fournissent un cadre intéressant pour décrire avec une résolution cellulaire le programme de développement d’un organisme complet. Pendant mon doctorat, j’ai développé une approche quantitative pour décrire l’évolution morphologique embryonnaire pendant le développement de Phallusia mammillata. J’ai ensuite utilisé cette approche pour systématiquement caractériser en détail les logiques des événements de spécifications de destin cellulaire.Pour caractériser quantitativement les comportements cellulaires pendant l’embryogenèse, nous avons utilisé de la microscopie à feuille de lumière multi-angles pour imager des embryons entiers à haute résolution spatio-temporelle. Les membranes plasmiques étaient marquées pour permettre l’identification des cellules. Pour extraire les informations biologiques de ce jeu de donnés, j’ai développé une nouvelle méthode pour segmenter les cellules en 4D, ASTEC. Une fois appliquée aux embryons de Phallusia mammillata imagés pendant 6 heures entre le stade 64 cellules et le début des stades bourgeon caudal, cette méthode a permis de récupérer la forme et de suivre 1030 cellules pendant 640 divisions. L’embryon digital 4D résultant peut être formalisé par un graphe dynamique, dans lequel les cellules sont représentées par des sommets reliés par des arrêtes représentant au sein d’un point de temps leur voisinage spatial, et entre différents points de temps leur lignage cellulaire.Basé sur cette représentation digitale et quantitative, nous avons systématiquement identifié les événements de spécification cellulaire jusqu’au dernier stade de la gastrulation. Des simulations informatiques ont révélé que des règles remarquablement simples intégrant les aires de contacts cellulaires et les expressions spatio-temporelles booléennes de signaux moléculaires extracellulaires sont suffisantes pour expliquer les inductions cellulaires au cours du développement précoce. Ce travail suggère que pour les embryons établissant des contacts stéréotypés et précis entre cellules voisines, les contraintes génomiques sont relâchées, ce qui permet une évolution plus rapide du génome. / Ascidian embryos develop with stereotyped and evolutionarily conserved invariant cell lineages to produce in a few hours or days tadpole larvae with a small number of cells. They thus provide an attractive framework to describe with cellular resolution the developmental program of a whole organism. During my PhD, I developed a quantitative approach to describe the evolution of embryonic morphologies during the development of the ascidian Phallusia mammillata. I then used this approach to systematically characterize in detail the logic of cell fate induction events. To quantitatively characterize cell behaviors during embryogenesis, we used multi-angle light-sheet microscopy to image with high spatio-temporal resolution entire live embryos with fluorescently labeled plasma membranes. To extract biological information from this imaging dataset, I then developed a conceptually novel automated method for 4D cell segmentation, ASTEC. Applied to a Phallusia mammillata embryo imaged for 6 hours between the 64-cell and the initial tailbud stages, this method allows the accurate tracking and shape analysis of 1030 cells across 640 cell divisions. The resulting 4D digital embryo can be formalized as a dynamic graph, in which cells are represented by nodes, linked within a time point by edges that represent their spatial neighborhood, and between time points by temporal edges describing cell lineages.Based on this quantitative digital representation, we systematically identified cell fate specification events up to the late gastrula stage. Computational simulations revealed that remarkably simple rules integrating measured cell-cell contact areas with boolean spatio-temporal expression data for extracellular signalling molecules are sufficient to explain most early cell inductions. This work suggests that in embryos establishing precise stereotyped contacts between neighboring cells, the genomic constraints for precise gene expression levels are relaxed, thereby allowing rapid genome evolution.

This thesis describes the chemical investigations of several ascidian species collected from the Great Barrier Reef, Queensland, Australia. The thesis is divided into two separate components, Part A focuses on the isolation and structure elucidation of 11 previously undescribed ascidian metabolites. All structures were assigned using a combination of spectroscopic and/or chemical methods. Part B relates to the isolation and chemical conversion of a natural product to a combinatorial template. The natural product template was subsequently used in the generation of a solution-phase combinatorial chemistry library. A further two combinatorial libraries were generated from a synthesised model compound that was related to the natural product template. Part A. Investigation of Aplidium longithorax collected from the Swains Reefs resulted in the isolation of two new para-substituted cyclofarnesylated quinone derived compounds, longithorones J (30) and K (31). The former compound had its absolute stereochemistry determined by the advanced Mosher method. From an Aplidium longithorax collected from Heron Island, two new cyclofarnesylated hydroquinone compounds, longithorols C (46) and D (47) and a novel macrocyclic chromenol, longithorol E (48) were isolated. Longithorol C (46) had its absolute stereochemistry determined by the advanced Mosher method. Chemical investigation of the deep-purple colonial ascidian, Didemnum chartaceum collected from Swains Reefs led to the isolation of five new lamellarin alkaloids, which included the 20-sulfated derivatives of lamellarins B (94), C (95) and L (96), the 8-sulfated derivative of lamellarin G (97) and the non-sulfated compound, lamellarin Z (98). The known lamellarins A (63), B (80), C (64), E (65), G (67), and L (71) plus the triacetate derivatives of lamellarin D (82) and N (83) were also isolated. An aberration in the integration of signals in the 1H NMR spectra of the 20-sulfated derivatives (94-96) led to NMR relaxation studies. T1 values were calculated for all protons in the sulfated lamellarins (94-97) and their corresponding non-sulfated derivatives (80, 64, 71, 67). The protons ortho to the sulfate group in compounds (94-97) had T1 values up to five times larger than the corresponding protons in their non-sulfated derivatives (80, 64, 71, 67). A specimen of Eudistoma anaematum collected from Heron Island was shown to contain a new b-carboline alkaloid, eudistomin V (130), in addition to the two known metabolites, eudistomin H (105) and I (106). Part B. The known natural products, 1,3-diphenethylurea (29), 1,3-dimethylxanthine (30), 1,3-dimethylisoguanine (31) and the salts of tambjamine C (16), E (18) and F (19) were isolated from the ascidian, Sigillina signifera collected in Blue Lagoon, Lizard Island. Base hydrolysis on mixtures of the salts of tambjamine C (16), E (18) and F (19) resulted in the production of 4-methoxy-2,2-bipyrrole-5-carbaldehyde (26). This natural product template (26) was used in the generation of an enamine combinatorial chemistry library (98, 103-111) using solution-phase parallel synthesis. The biaryl compound, 4-(2-thienyl)-1H-pyrrole-2-carbaldehyde (59) was successfully synthesised using Suzuki-Miyaura coupling conditions and subsequently used as a template in the generation of an amine (67, 77, 80-87) and imine (78, 92-95) combinatorial library using solution-phase parallel synthesis.

Comment la morphogenèse embryonnaire peut-elle être conservée malgré une divergence importante des séquences codantes et non-codantes ? Pour répondre à cette question, nous avons travaillé sur le développement précoce d’ascidies divergentes, Phallusia mammillata et Ciona intestinalis. Ces espèces partagent une morphogénèse pratiquement identique et des lignages cellulaires stéréotypés. Or, leurs génomes sont tellement divergents que leurs séquences ne peuvent pas être alignées.Nous avons choisi d’étudier les cellules précurseuses de l’endoderme au cours de deux processus développementaux conservés : spécification du destin et la gastrulation. Nous avons comparé par hybridation in situ l’expression transcriptionelle des gènes régulateurs orthologues dans Phallusia et Ciona. Nous avons trouvé que l’expression dans l’endoderme de 8 gènes régulateurs impliqués dans ces processus développementaux est qualitativement conservée entre les deux espèces.Pour étudier comment ces gènes ont conservé leur régulation malgré une divergence non-codante importante, nous avons collaboré avec l’équipe Gomez-Skarmeta pour cartographier, par ATAC-seq, la chromatine ouverte dans les deux espèces pour identifier les régions régulatrices actives à l’échelle du génome. 35 sur les 39 séquences ouvertes avoisinant les gènes de l’endoderme ont été trouvé active avant le stade larval, par éléctroporation. La plupart des séquences testées ont conservé leur activité dans les deux espèces malgré la divergence de séquence. Nous avons alors identifié des sites de fixations pour facteurs de transcription potentiels se trouvant dans les enhancers pour l’endoderme pour identifier les régulateurs dans Phallusia et Ciona.Nos résultats suggèrent des changements assez importants de l’ordre des sites de fixations sans pour autant avoir de changement dans l’architecture dans les réseaux de gènes régulateurs ; ceci explique la conservation qualitative de l’expression des gènes entre ces ascidies divergentes. En outre, nous avons trouvé que les shadow enhancers sont plus répandus qu’anticipé. / How can embryonic morphogenesis be evolutionarily conserved in spite of extensive divergence in coding and non-coding genome sequences? To address this question, we worked on the early development of two very divergent ascidians, Phallusia mammillata and Ciona intestinalis. These species share an almost identical early morphogenesis and stereotyped cell lineages. Remarkably, however, their genomes are divergent to the extent that their non-coding sequences cannot be aligned and gene order has not been conserved.We focus our attention on the behaviour of endoderm precursors throughout two important evolutionarily conserved developmental processes: initial fate specification and early gastrulation. We first compared by in situ hybridisation the transcriptional expression of orthologous regulatory genes in Phallusia and in Ciona. We found that the endodermal expression of 8 regulatory genes known to be involved in these developmental processes is qualitatively conserved between the two species.To study how these genes conserved their regulation in spite of extensive non-coding sequence divergence, we collaborated with the Gomez-Skarmeta lab to map, by ATAC-seq, open chromatin regions in both species to identify active regulatory regions genomewide. Three quarters of the 39 open chromatin regions for endodermal genes behaved as active regulatory sequences by the larval stage, when tested by electroporation in embryos. Many of the tested sequences had conserved cis-regulatory activity in both species in spite of sequence divergence. We have identifed putative transcription factor binding sites in endodermal enhancers in both species to identify conserved upstream regulators shared between Phallusia and Ciona.Taken together our results suggest that extensive transcription factor binding site turn over, without radical change in GRNs architecture, may explain the qualitative conservation of gene expression patterns between highly divergent ascidian genomes. Furthermore, we found that shadow enhancers are much more prevalent than initially anticipated.Taken together our results suggest that extensive transcription factor binding site turn over, without radical change in GRNs architecture, may explain the qualitative conservation of gene expression patterns between highly divergent ascidian genomes. Furthermore, we found that shadow enhancers are much more prevalent than initially anticipated.

Precise descriptions and comprehensive taxonomies of species and their ecology are essential in monitoring changes in marine biodiversity at multiple spatial scales. A currently undescribed species of commensal amphipod in the genus Leucothoe is reported from New Zealand, collected from the endemic tunicate Cnemidocarpa bicornuta. This species differs from others in the genus in having a one-articulate first maxilla palp and an apically produced tuberculate lobe on the inner margin of the outer plate of the maxilliped. Previous taxonomic surveys in New Zealand waters did not document this species, indicating that it may be a recent arrival. This research highlights the importance of biodiversity monitoring and taxonomic surveys to record occurrences of undescribed or recently-arrived taxa.

En biologie développementale, l'étude d'organismes modèles vise à comprendreles mécanismes génétiques responsables de la morphogenèse chez le vivant. Lamicroscopie confocale à fluorescence permet aujourd'hui d'observer in vivo àl'échelle de la cellule et avec une haute fréquence temporelle le développementd'organismes. Les séquences d'images 3D+t ainsi obtenues nécessitent d'avoirdes outils de traitement d'images adaptés.Dans cette thèse, nous construisons des outils dédiés à l'étude dudéveloppement de deux organismes, l'embryon de l'ascidie Phallusiamammillata et le bouton floral d'Arabidopsis thaliana.Nous développons d'abord une méthode de comparaison de segmentationsadaptée aux images de tissus épithéliaux d'organismes en développement.Nous nous appuyons sur cet outil pour valider notre seconde contribution quiporte sur la mise en place d'un outil de détection et de reconstruction demembranes cellulaires conçu afin de procéder à la segmentation de cellulesdans les images d'ascidies et d'arabidopsis.Nous utilisons ensuite l'outil de segmentation de membranes précédemmentintroduit pour construire une stratégie de recalage spatial inter-individusappliquée aux embryons d'ascidies. Enfin, nous élaborons une stratégie derecalage spatio-temporel inter-individus appliquée à des séquences d'images 3Dde méristèmes floraux / In developmental biology, the study of model organisms aims for theunderstanding of genetic mechanisms responsible of morphogenesis. Today,fluorescent confocal microscopy is a means for in vivo imaging of developingorganisms at cell level with a high spatio-temporal resolution. To handle such3D+t image sequences, adapted computer-assisted methods are highlydesirable.In this thesis, we build dedicated tools for the study of two developingorganisms, the ascidian Phallusia mammillata's embryo and the Arabidopsisthaliana's floral meristem.We first develop a method for segmentation comparison adapted to developingorganism epithelial tissue images. This tool is then used to validate our secondcontribution that is about the development of a cell membranes detection andreconstruction tool for cell shape segmentation process applied to ascidian andarabidopsis images.We then use the previously introduced membrane detection tool to build aninter-individual spatial registration strategy applied to ascidian embryo images.Finally, we develop an inter-individual spatio-temporal registration strategyapplied to 3D image sequences of arabidopsis floral meristems

Abstract Die Phorbazole und Diazonamide sind Naturstoffe marinen Ursprungs. Als strukturelle Gemeinsamkeiten zeichnen sie sich durch einen oder mehrere Oxazol-Ringe sowie durch das Vorhandensein von Chloratomen aus. In der vorliegenden Arbeit wurde erstmals eine Totalsynthese von Phorbazol C entwickelt, ausgehend von p-Hydroxybenzaldehyd und 2- Methylpyrrol-5-carbonsäureethylester. In den Schlüsselschritten wurden die Bausteine über eine Amidbindung verknüpft und der Oxazolring durch Cyclodehydratisierung aufgebaut. Für das 4-Chloroxazol-haltige Phorbazol A wurde ein alternativer Syntheseweg gewählt. Dieser führte jedoch wegen einer unerwarteten Umlagerungsreaktion zu einem neuem Konstitutionsisomeren der Zielstruktur. Für das komplex aufgebaute Diazonamid A wurde eine Retrosynthese entwickelt und entsprechende Modellreaktionen durchgeführt. Dabei wurden Indolyl-4-Chloroxazole mit verschiedenen Substituenten synthetisiert. Für die Synthese von 2,2-Diarylessigsäureestern erwiesen sich Chromarenkomplexe als geeignete Elektrophile. Die Einführung eines weiteren Substituenten zum Aufbau des quartären Kohnelstoffatoms gelang in nur mäßigen Ausbeuten. Hier führten Bleiarylverbindungen zum Erfolg. / Abstract Phorbazoles and Diazonamides are marine natural products. They share one or more oxazole rings and the presence of chloro atoms as common structural features. The present thesis describes the first total synthesis of Phorbazole C, starting from p-hydroxybenzaldehyde and 2-methylpyrrol-5-ethylcarboxylate. As key step the building blocks were connected as amide. The oxazole-ring was formed via cyclo- dehydration. An alternative synthetic approach was chosen for Phorbazole A that contains a 4-chloro- oxazole. This led to a new constitutional isomer of the lead structure due to an usual rearrangement. For the complex structure of Diazonamide A a retrosynthetic approach was developed. Different key structures were examined by model reactions. As a result, indolyl-4- chlorooxazoles with various substituents were synthesized. A second arene ring was introduced into 2-aryl-acetic acid by chromium fluoroarene complexes as electrophiles. The introduction of another substituent in order to establish the quaternary carbon atom was accomplished in low yields. Lead aryl compounds turned out to be advantageous in this reaction.