L’induction neurale est le processus au travers duquel les cellules ectodermiques de l’embryon deviennent neurales. De nombreuses études sur les mécanismes contrôlant ce processus on été réalisées mais du fait de sa complexité, de nombreuses questions restent sans réponse. Au cours de ce travail de thèse, je me suis intéressé à l’étude de l’induction neurale sous une perspective évolutive en étudiant ce processus chez le céphalocordé amphioxus, l’un des plus proches parents des vertébrés. J’ai pu mettre en évidence que, comme les vertébrés, l’amphioxus possède un organisateur. J’ai également confirmé une conservation du rôle des voies de signalisation BMP et FGF respectivement dans l’induction de l’épiderme et la régionalisation du tissu neural. Cependant, au contraire des vertébrés, le signal FGF ne semble pas être un acteur prépondérant de l’induction neurale. Au contraire, un rôle important de la voie de signalisation Activine/Nodal a été mis en évidence.Les résultats obtenus soutiennent d’une part la conservation de certains aspects de ce mécanisme chez tous les chordés, et suggèrent d’autre part l’implication de certains acteurs comme la voie Activine/Nodal jusque là inconnue chez les vertébrés. La position phylogénétique de l’amphioxus et la conservation globale de ce processus entre les céphalochordés et les vertébrés nous permettent de suggérer que l’ancêtre des chordés formait du tissue neurale au travers des mécanismes mis en évidence dans cet étude. Ces résultats nous permettent également de proposer de nouvelles études chez les vertébrés visant à établir un rôle putatif de la voie Activine/Nodal au cours de ce processus, rôle jusque la complètement inconnu. / Neural induction is the process through which embryonic ectodermal cells become neural. Many studies on the mechanisms controlling this process have been made, but because of its complexity, many questions remain unanswered. In this thesis, I have focused my interest on the study of neural induction in an evolutionary context studying this process in the cephalochordate amphioxus, one of the closest relatives of vertebrates. I have highlighted that amphioxus, as vertebrates, possesses an organizer. I have demonstrated a conservation of the role of BMP and FGF signals in the induction of the epidermis and the regionalization of neural tissue respectively. However, in contrast to vertebrates, FGF signal does not appear to be a major player in neural induction. Instead, an important role of Activin/Nodal signaling pathway has been demonstrated. These results support, first, the conservation of several aspects of this mechanism in all chordates, and second, they suggest the involvement of the Activin/Nodal signaling in this process, something previously unknown in vertebrates. The phylogenetic position of amphioxus and the overall conservation of this process between cephalochordates and vertebrates allow us to suggest that the ancestor of chordates formed its neural tissue through mechanisms highlighted in this study. These results also allow us to propose new studies in vertebrates for establishing a putative role of the Activin/Nodal signaling during this process, a role previously completely unknown.

Animal chemosensation involves several families of G protein-coupled receptors (GPCRs) and, though some of these families are well characterized in vertebrates and nematode worms, receptors have not been identified for most metazoan lineages. In this dissertation, I use a combination of bioinformatics approaches to identify candidate chemosensory receptors in three invertebrates that occupy key positions in the metazoan phylogeny. In the sea urchin Strongylocentrotus purpuratus, I uncovered 192 candidate chemosensory receptors many of which are expressed in sensory structures including pedicellariae and tube feet. In the cephalochordate Branchiostoma floridae, my survey uncovered 50 full-length and 11 partial odorant receptors (OR). No ORs were identified in the urochordate Ciona intestinalis. By exposing conserved amino acid motifs and testing the ability of those motifs to discriminate between ORs and non-OR GPCRs, I identified three OR-specific amino acid motifs that are common in cephalochordate, fish and mammalian ORs and are found in less than 1% of non-ORs from the rhodopsin-like GPCR family. To further investigate the antiquity of vertebrate ORs, I used the OR-specific motifs as probes to search for orthologs among the protein predictions from 12 invertebrates. My search uncovered a novel group of genes in the cnidarian Nematostella vectensis. Phylogenetic analysis that included representatives from the major subgroups of rhodopsin-like GPCRs showed that the cnidarian genes, the cephalochordate and vertebrate ORs, and a subset of genes S. purpuratus from my initial survey, form a monophyletic clade. The taxonomic distribution of these genes indicates that the formation of this clade began at least 700 million years ago, prior to the divergence of cnidarians and bilaterians. Furthermore, my phylogenetic analyses show that three of the four major subgroups of rhodopsin-like GPCRs existed in the ancestor of cnidarians and bilaterians. The utility of the new genes I describe here is that they can be used to identify candidate olfactory cells and organs in cnidarians, echinoderms and cephalochordates that can be tested for function. These genes also provide the raw material for surveys of other metazoans as their genomes become available. My sequence level comparison between chordates, echinoderms and cnidarians exposed several conserved amino acid positions that may be useful for understanding receptor mediated signal transduction. ORs and other rhodopsin-like GPCRs have roles in cell migration, axon guidance and neurite growth; therefore duplication and divergence in the rhodopsin-like gene family may have played a key role in the evolution of cell type diversity (including the emergence of complex nervous systems) and in the evolution of metazoan body plan diversity. / Graduate