Use this URL to cite or link to this record in EThOS:
Title: Roles of Reelin and Disabled1 in neural development in zebrafish
Author: Costagli, A.
Awarding Body: University of London
Current Institution: University College London (University of London)
Date of Award: 2007
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Reelin and Disabled 1 (Dab1) are known to be involved in neuronal migration in vertebrates and in particular in radial migration. Reelin is a secreted protein that can bind several receptors and the signal is intracellular transduced by Dabl. The final targets of the Reelin pathway are molecules that regulate cytoskeletal remodeling. In my project I studied the expression pattern of reelin and dabl in several areas of the zebrafish CNS. The differences found in the telencephalic expression of reelin and dabl between teleosts and tetrapods are likely to arise from the process of eversion, which is specific for the teleost telencephalon. On the contrary, all the other regions of the CNS present a conservative pattern of expression, in comparable structures among vertebrates, with the only exception of the olfactory bulb that does not express reelin in zebrafish. As the dabl gene shows a high degree of complexity in mammals and mice, I studied the genomic organization of the dabl gene in zebrafish and found a similarly complex organization. In order to study the functions of the Reelin pathway in neuronal migration in zebrafish, I performed loss of function experiments with morpholino antisense oligonucleotides. I found defects at level of several neuronal groups including the facial branchiomotor nucleus, the Mauthner neurons and neural crests. To investigate whether the role of dabl in the migration of these neuronal groups may be that of conveying a Reelin signal, I attempt to rescue these phenotypes by overexpressing full length dabl or truncated forms of the protein that lack the Reelin or the CDK5 responsive domains. It appears that the presence of the tyrosine domain, but not of the CDK5 phosphorylation domain, is necessary for partial resoiing of most of these phenotypes. I also found that some populations of neurons that express dabl show defects in neurites growth in morpholino injected embryos.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available