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Small Molecule Developmental Screens Reveal the Logic and Timing of Vertebrate Development

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Specialty Science
Date 2000 Nov 23
PMID 11087852
Citations 157
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Abstract

Much has been learned about vertebrate development by random mutagenesis followed by phenotypic screening and by targeted gene disruption followed by phenotypic analysis in model organisms. Because the timing of many developmental events is critical, it would be useful to have temporal control over modulation of gene function, a luxury frequently not possible with genetic mutants. Here, we demonstrate that small molecules capable of conditional gene product modulation can be identified through developmental screens in zebrafish. We have identified several small molecules that specifically modulate various aspects of vertebrate ontogeny, including development of the central nervous system, the cardiovascular system, the neural crest, and the ear. Several of the small molecules identified allowed us to dissect the logic of melanocyte and otolith development and to identify critical periods for these events. Small molecules identified in this way offer potential to dissect further these and other developmental processes and to identify novel genes involved in vertebrate development.

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References
1.
Mayer T, Kapoor T, Haggarty S, King R, Schreiber S, Mitchison T . Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen. Science. 1999; 286(5441):971-4. DOI: 10.1126/science.286.5441.971. View

2.
Gaffield W, Incardona J, Kapur R, Roelink H . A looking glass perspective: thalidomide and cyclopamine. Cell Mol Biol (Noisy-le-grand). 1999; 45(5):579-88. View

3.
Schreiber S . Target-oriented and diversity-oriented organic synthesis in drug discovery. Science. 2000; 287(5460):1964-9. DOI: 10.1126/science.287.5460.1964. View

4.
Blader P, Strahle U . Zebrafish developmental genetics and central nervous system development. Hum Mol Genet. 2000; 9(6):945-51. DOI: 10.1093/hmg/9.6.945. View

5.
KEELER R . Teratogenic compounds of Veratrum californicum (Durand) X. Cyclopia in rabbits produced by cyclopamine. Teratology. 1970; 3(2):175-80. DOI: 10.1002/tera.1420030210. View