Skip to main content

Spastic paraplegia genes and endosomal signaling in Drosophila

Objective

The hereditary spastic paraplegias (HSPs) are a group of neurodegenerative conditions characterised by the degeneration of longer spinal cord motor tract axons. The normal function of the 13 cloned spastic paraplegia genes (SPGs) is largely unknown, but most encode intracellular membrane-associated proteins. Recently, the host laboratory has established that one of these genes, SPG6, encodes an endosomal regulator of BMP receptor trafficking, and regulates synaptic growth and axonal microtubules via this effect. The aim of this project is to test whether other intracellular membrane SPG products also function in receptor membrane trafficking and signalling, particularly in the BMP pathway. The focus of the study will be on the three SPGs currently most amenable to study in Drosophila melanogaster, a model system with proven power in this area. Top priority will be given to the recently identified spastizin (SPG15), an endosomal localised protein containing a FYVE motif, found on proteins that function in the regulation of endocytic trafficking. Mutants of the Drosophila SPG15 homologue will be generated to study phenotypes, particularly at the neuromuscular junction (NMJ). Also, antibodies will be generated to investigate spastizin colocalisation and association with BMP, Wnt, and Notch pathway subunits. In addition, I will use similar approaches to test two other membrane associated SPG products: spastin (SPG4) and atlastin (SPG3A). These are among the most commonly mutated SPGs, thus Drosophila stocks and reagents are already available, but their potential role in regulating endosomal trafficking pathways is not well studied. This investigation, into the functional pathways of spastizin, spastin, and atlastin, will further the understanding of the mechanism of action of mutated proteins in motor neuron degeneration.

Field of science

  • /natural sciences/biological sciences/biochemistry/biomolecules/proteins

Call for proposal

FP7-PEOPLE-IEF-2008
See other projects for this call

Funding Scheme

MC-IEF - Intra-European Fellowships (IEF)

Coordinator

THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE
Address
Trinity Lane The Old Schools
CB2 1TN Cambridge
United Kingdom
Activity type
Higher or Secondary Education Establishments
EU contribution
€ 170 733,61
Administrative Contact
Edna Murphy (Ms.)