Award details

Mechanisms mediating intracellular sorting of Roundabout

Reference	BB/G022399/1
Principal Investigator / Supervisor	Professor Guy Justin Clive Tear
Co-Investigators / Co-Supervisors
Institution	King's College London
Department	MRC Ctr for Developmental Neurobiology
Funding type	Research
Value (£)	346,798
Status	Completed
Type	Research Grant
Start date	01/07/2009
End date	30/06/2012
Duration	36 months

Abstract

Cells must accurately regulate their ability to send and receive signals during normal homeostasis and development. Regulation of receptor protein trafficking is an important mechanism, whereby proteins are localised to different compartments or regions in the cell, to modulate their activity. It has been identified in both mice and Drosophila that the regulated spatial distribution of Robo proteinsin commissural axons is crucial for their ability to navigate the midline of the central nervous system (CNS). In Drosophila, Commissureless acts on the Roundabout receptor to regulate its cellular distribution. As neurons approach the midline Commissureless sorts Roundabout to an intracellular location whereas after the axons cross the midline Commissureless activity is reduced and Roundabout reaches the cell surface. Once Roundabout is at the cell surface it acts to receive the midline derived repellent signal Slit. Little is known about how this mechanism is regulated and we propose to study how Roundabout is distributed in the growing axons during the development of the CNS. We propose to examine in more detail the localisation of the proteins in neurons as they approach and cross the midline using time-lapse studies. This will allow us to identify the nature of the intracellular compartment occupied by Commissureless as neurons extend along their pathway and the precise dynamics of Commissureless and Roundabout trafficking. We also propose to identify additional components of this mechanism using an affinity chromatography approach to identify molecules that bind a region of Comm essential for its function. Although it was previously suggested that the ubiquitin ligase Nedd4 may be a key mediator of Comm activity in commissural neurons this has been challenged and we have confirmed that Nedd4 may not be essential for this process. We therefore seek to identify additional proteins that function with Comm to regulate Robo protein distribution.

Summary

We are dependent on our nervous system functioning correctly for us to move, think, learn, speak and control our bodies. To do this all our nerve cells must connect up in the brain and to the parts of the body they control. Most of this 'wiring together' happens during the growth and development of the embryo in pregnancy. To do this each nerve cell must extend a long process, called an axon, over large distances and through complex environments to find and connect to its appropriate partners. Each axon is guided when to turn and which way to grow to reach its partner by sensing specific chemicals or molecular 'cues' in different parts of the body. These signals are detected by 'receptor' proteins at the tip of the growing axon. The activity of these receptors change as the axons grow into different regions, We want to find the molecules that work to control the activity of these receptors as they guide axons along their pathways. We know already that many of the same molecules and receptors in mammals are also present in smaller animals like the fruitfly Drosophila where they do the same job but on a simpler scale. We are using Drosophila to characterise how one of these receptors called Roundabout is regulated in a subset of neurons. We know that Roundabout must be precisely regulated for axons to grow correctly. Although we have identied one key regulator of the Roundabout protein, a protein called Commissureless we do not know precisely how this molecule acts to regulate Roundabout. We plan to use Drosophila as a model system where we can watch exactly how the Roundabout and Commissureless molecules behave in the axons as they grow. This will give us information on the dynamics of the process. We also use Drosophila as a model system to rapidly identify and test the role of further molecules that may act in this process, e.g. those that bind to Commissureless. By using Drosophila we can reduce the need to sacrifice large numbers of mice in research. Once wehave found out how these molecules work in Drosophila we will inform other researchers so that the molecules can be tested in other model systems. We need this information both to learn how the nervous system is made and to find out what molecules might be useful in helping us to repair neural injuries or diseases that lead to paralysis or neural degeneration. Unfortunately mammals cannot repair nerve damage that occurs in the brain, our hope is that by identifying the molecules that were originally used to drive and direct nerve cell growth in the embryo we can re-supply these molecules to help nerve cell regeneration in people.

Committee	Closed Committee - Genes & Developmental Biology (GDB)
Research Topics	Neuroscience and Behaviour
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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