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Model Organisms in Drug Discovery

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4<br />

Drosophila as a Tool for <strong>Drug</strong><br />

<strong>Discovery</strong><br />

Hao Li and Dan Garza<br />

Comparative genomics of humans and Drosophila demonstrates a high degree<br />

of conservation both at the level of molecular build<strong>in</strong>g blocks (genes) and at the<br />

level of disease-relevant pathways (gene networks). This conservation provides<br />

the basis for at least four major areas of Drosophila application <strong>in</strong> drug<br />

discovery: discovery of drug targets, mechanism-of-action studies, compound<br />

screen<strong>in</strong>g and genotoxicity tests. This chapter discusses how fly models of<br />

human diseases can be established and utilized <strong>in</strong> the four areas of drug<br />

discovery. We also <strong>in</strong>clude a brief discussion of the available experimental tools<br />

and high throughput tools that need to be developed further.<br />

4.1 Drosophila as a model organism for biomedical science<br />

Introduction<br />

One of the major paradigms <strong>in</strong> today’s basic biomedical research is to use<br />

experimentally tractable model organisms to study human gene function. For<br />

nearly a century, the fruit fly Drosophila melanogaster has been utilized as a<br />

genetic system to study a variety of basic biological processes. Several features<br />

make Drosophila attractive as a model organism for genetic and biomedical<br />

research. First, Drosophila is easily cultured <strong>in</strong> the laboratory. Flies are small<br />

(ca. 1 mm), have a life cycle of less than 2 weeks and grow on simple cornmeal/<br />

<strong>Model</strong> <strong>Organisms</strong> <strong>in</strong> <strong>Drug</strong> <strong>Discovery</strong>. Edited by Pamela M. Carroll and Kev<strong>in</strong> Fitzgerald<br />

Copyright © 2003 John Wiley & Sons, Ltd. ISBN: 0-470-84893-6

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