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Molecular and Cellular Biology, October 2006, p. 7178-7189, Vol. 26, No. 19
0270-7306/06/$08.00+0 doi:10.1128/MCB.00130-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Stowers Institute for Medical Research, 1000 E. 50th St., Kansas City, Missouri 64110
Received 21 January 2006/ Returned for modification 3 March 2006/ Accepted 17 July 2006
Histone acetylation provides a switch between transcriptionally repressive and permissive chromatin. By regulating the chromatin structure at specific promoters, histone acetyltransferases (HATs) carry out important functions during differentiation and development of higher eukaryotes. HAT complexes are present in organisms as diverse as Saccharomyces cerevisiae, humans, and flies. For example, the well-studied yeast SAGA is related to three mammalian complexes. We previously identified Drosophila melanogaster orthologues of yeast SAGA components Ada2, Ada3, Spt3, and Tra1 and demonstrated that they associate with dGcn5 in a high-molecular-weight complex. To better understand the function of Drosophila SAGA (dSAGA), we sought to affinity purify and characterize this complex in more detail. A proteomic approach led to the identification of an orthologue of the yeast protein Ada1 and the novel protein encoded by CG4448, referred to as WDA (will decrease acetylation). Embryos lacking both alleles of the wda gene exhibited reduced levels of histone H3 acetylation and could not develop into adult flies. Our results point to a critical function of dSAGA and histone acetylation during Drosophila development.
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