Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600276
Title: Functional analysis of the kekkon genes in the Drosophila nervous system
Author: Bishop, Simon
Awarding Body: University of Birmingham
Current Institution: University of Birmingham
Date of Award: 2014
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Abstract:
The canonical vertebrate neurotrophin receptors — the Trk and p75\(^N\)\(^T\)\(^R\) protein families — have not been found in Drosophila, thus it is unclear how neurotrophic signalling is implemented in fruit flies. The Drosophila genome encodes 9 proteins with extracellular domain compositions resembling vertebrate Trks, but lacking an intracellular tyrosine kinase. Here, I investigated whether these 9 proteins, plus 3 further candidates, can function as receptors of the Drosophila neurotrophins (DNTs). Initial characterisation of the candidate proteins highlighted the Kekkon (Kek) family as potential receptors. After tool and mutant generation, I showed that: (1) kek2, kek3 and kek6 overexpression rescues the semi-lethality of DNT1DNT2 double mutants; (2) Kek3, Kek4 and Kek6 interact with DNT2 ligand, eliciting a luciferase readout in S2 cells; and (3) kek3, kek4 and kek6 genetically interact with DNT1 and DNT2. Further analysis revealed Kek6 is expressed in, and required for targeting of, motor neurons, and has a role in locomotion. Surprisingly, Kek4 was enriched in the larval ring gland and affected developmental timing by inhibiting juvenile hormone. Together, data revealed the Keks function in neurodevelopment and growth regulation, and interact with the DNTs. The work uncovered functional conservation of protein domains in neurodevelopment despite domain shuffling throughout the animal kingdom.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.600276  DOI: Not available
Keywords: QH301 Biology
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