80 research outputs found
Making sense of zebrafish neural development in the Minervois
The meeting 'From sensory perception to motor output: genetic bases of behavior in the zebrafish embryo' was held at Minerve (South of France) on March 16–18, 2007. The meeting site was beautifully situated in the heart of the Minervois wine country, and its remoteness promoted conversations and interaction over the course of the program. The meeting covered neurogenesis and eye development on day 1, ear and lateral line development on day 2, and brain connectivity and behavior on day 3. Underlying all sessions, however, ran the growing importance of live imaging, an approach that takes full advantage of the transparency of fish embryos and early larvae, as illustrated by several movies and links in this report
Control of cell migration in the development of the posterior lateral line: antagonistic interactions between the chemokine receptors CXCR4 and CXCR7/RDC1
BACKGROUND: The formation of the posterior lateral line of teleosts depends on the migration of a primordium that originates near the otic vesicle and moves to the tip of the tail. Groups of cells at the trailing edge of the primordium slow down at regular intervals and eventually settle to differentiate as sense organs. The migration of the primordium is driven by the chemokine SDF1 and by its receptor CXCR4, encoded respectively by the genes sdf1a and cxcr4b. cxcr4b is expressed in the migrating cells and is down-regulated in the trailing cells of the primordium. sdf1a is expressed along the path of migration. There is no evidence for a gradient of sdf1a expression, however, and the origin of the directionality of migration is not known. RESULTS: Here we document the expression of a second chemokine receptor gene, cxcr7, in the migrating primordium. We show that cxcr7 is highly expressed in the trailing cells of the primordium but not at all in the leading cells, a pattern that is complementary to that of cxcr4b. Even though cxcr7 is not expressed in the cells that lead primordium migration, its inactivation results in impaired migration. The phenotypes of cxcr4b, cxcr7 double morphant embryos suggest, however, that CXCR7 does not contribute to the migratory capabilities of primordium cells. We also show that, in the absence of cxcr4b, expression of cxcr7 becomes ubiquitous in the stalled primordium. CONCLUSION: Our observations suggest that CXCR7 is required to provide directionality to the migration. We propose that directionality is imposed on the primordium as soon as it comes in contact with the stripe of SDF1, and is maintained throughout migration by a negative interaction between the two receptors
Wnt/Dkk Negative Feedback Regulates Sensory Organ Size in Zebrafish
SummaryCorrect organ size must involve a balance between promotion and inhibition of cell proliferation. A mathematical model has been proposed in which an organ is assumed to produce its own growth activator as well as a growth inhibitor [1], but there is as yet no molecular evidence to support this model [2]. The mechanosensory organs of the fish lateral line system (neuromasts) are composed of a core of sensory hair cells surrounded by nonsensory support cells. Sensory cells are constantly replaced and are regenerated from surrounding nonsensory cells [3], while each organ retains the same size throughout life. Moreover, neuromasts also bud off new neuromasts, which stop growing when they reach the same size [4, 5]. Here, we show that the size of neuromasts is controlled by a balance between growth-promoting Wnt signaling activity in proliferation-competent cells and Wnt-inhibiting Dkk activity produced by differentiated sensory cells. This negative feedback loop from Dkk (secreted by differentiated cells) on Wnt-dependent cell proliferation (in surrounding cells) also acts during regeneration to achieve size constancy. This study establishes Wnt/Dkk as a novel mechanism to determine the final size of an organ
The developmental biology of neural connectivity
How can the development of an ordered array of neuronal connections be encoded in the genome? Results on the establishment of sensory connections in insects indicate that this programming is a multi-stepped process which begins as soon as the first axons develop. Because each step relies on the previous level of organization, the first steps of the process are subject to intense structural constraints, and therefore have been largely conserved through evolution. What is known of the molecular biology of some essential steps, like the differentiation of excitable cells, their aggregation in nerve cords, and the diversification of a periodic structure, supports the idea that the basic organization of the CNS evolved before the divergence between the chordate and the arthropod/annelid lineage.SCOPUS: re.jinfo:eu-repo/semantics/publishe
Le développement du système nerveux chez la drosophile
Doctorat en Sciencesinfo:eu-repo/semantics/nonPublishe
Etude de mutants affectés dans la traduction ou la transcription
Doctorat en Sciencesinfo:eu-repo/semantics/nonPublishe
Le développement du système nerveux chez la drosophile.
The formation of sense organs in Drosophila involves a series of choices, each of which depends on the co-ordinated activity of a small battery of genes. Two essential steps of this process have been extensively studied over the past few years: the determination of neural precursor cells, and their diversification. In both cases, the choices are dichotomous, and each choice reflects the fact that a specific control gene is or is not expressed. This principle is illustrated in the case of the genes "cut" and "poxn", the expression of which controls the type of sense organ that a given precursor will form.SCOPUS: ar.jinfo:eu-repo/semantics/publishe
Neuronal Connectivity: Bis Repetita Placent
AbstractThe mechanism that allows a sensory neuron to extend its terminal branches along the appropriate fascicle within the CNS turns out to be the same as that which positioned the fascicle earlier on, and the gene that controls this position is the same as that which determined the neuron's identity
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