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Using chemical tools to study Wnt signalling in neural development

Reference	BB/E013872/1
Principal Investigator / Supervisor	Professor Karen Liu
Co-Investigators / Co-Supervisors
Institution	King's College London
Department	Craniofacial Dev Orthodon and Microbiol
Funding type	Research
Value (£)	347,224
Status	Completed
Type	Research Grant
Start date	01/10/2007
End date	30/09/2010
Duration	36 months

Abstract

The Wnt/beta-catenin signalling pathway is evolutionarily conserved and plays important roles in proliferation and patterning. While this pathway has been well studied genetically and developmentally, many of the biochemical interactions remain unclear. Building new molecular tools to study Wnt signalling will provide important insight into a variety of biological processes. I have available a mouse carrying a drug-dependent knock-in of GSK-3beta. This allele of GSK-3beta is a 'drug-on' allele; in the presence of a rapamycin analogue, GSK-3beta protein function is restored. In the absence of drug, this allele phenocopies a conventional knockout of GSK-3beta. Because our mutant is a knock-in, endogenous protein is properly localized and active when treated with drug. To develop more tools for studying the Wnt pathway, additional specific, fast-acting, drug-sensitive protein alleles are being constructed and tested using Xenopus as a rapid assay system. These proteins are then being used to study anterior patterning of the embryonic axis and subcellular requirements of GSK-3beta.

Summary

Studying the functions of specific proteins by inactivation within an intact animal presents several challenges. Genetic deletion, or 'knockout,' technology completely eliminates a protein, but since the protein may have roles in different tissues or at different stages of development, a knockout mouse may not survive to the desired stage of maturity. Pharmacologic approaches are attractive alternatives because small molecules can be used to inhibit protein function in a genetically normal animal, they can be administered and removed at specific times and are thus reversible, and they often provide attractive lead compounds for drug development. However, small molecules present their own challenges. Is there a small molecule that targets the protein of interest? Can it be delivered to a live animal? Most importantly, can off-target effects of the small molecule be minimized? To study the function of signaling proteins in development I am combining the advantages of gene targeting and small molecules, using a novel approach called inducible stabilization in which a non-toxic drug regulates the stability of any specific protein of interest. As an embryo develops and grows, each cell must be precisely coordinated with its neighbors in order for the animal to be properly patterned. These cells must be communicating with surrounding tissues and making cell fate decisions at all times. How do cells know which stimuli to respond to and which stimuli to ignore? A more thorough understanding of what key signaling molecules are doing in specific types of cells will give us a better understanding of how an animal is built, as well as what happens when development goes awry. My work aims to address these questions by adapting novel chemical tools to help us better understand embryonic development. A major problem when studying developmental processes is that these processes occur over time. For example, first the embryo makes neural precursors, then it allocates some ofthese cells to become different types of neural tissue. Meanwhile, because the embryo is growing and changing in shape, all these tissues need to development and be moved to the right place at the right time. Somehow the cells can sense an 'architectural plan' and coordinate to make brains in the head and motor neurons precisely where the limbs are developing. My work currently focuses on a signaling protein called GSK-3 in Wnt signalling, a pathway known to be important for the development of the neural axis. Early in development, Wnt signalling is thought be important for patterning the posterior part of the embryo. Too much Wnt activation results in a truncation of anterior head structures while inhibiting Wnts results in enlarged head structures. GSK-3 plays an opposing role in the Wnt pathway and presumably helps to maintain a balance in the amount of signals received in different parts of the animal. My work allows us to manipulate GSK-3 levels during embryogenesis with much finer control than previously available. In addtion, I can control the localization of GSK-3 within the cell, moving it into and out of the nucleus using a drug. The new chemical tools I am using may be applicable to other proteins as well which would provide a whole new set of tools to study development.

Committee	Closed Committee - Genes & Developmental Biology (GDB)
Research Topics	X – not assigned to a current Research Topic
Research Priority	X – Research Priority information not available
Research Initiative	Selective Chemical Intervention in Biological Systems (SCIBSII) [2006]
Funding Scheme	X – not Funded via a specific Funding Scheme

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