The Zinc Finger-Associated Domain of the Drosophila Transcription Factor Grauzone Is a Novel Zinc-Coordinating Protein-Protein Interaction Module
About one-third of the more than 300 C2H2 zinc finger proteins of Drosophila contain a conserved sequence motif, the zinc finger-associated domain (ZAD). Genes that encode ZAD proteins are specific for and expanded in the genomes of insects. Only three ZAD-encoding gene functions are established, an...
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Veröffentlicht in: | Structure (London) 2003-11, Vol.11 (11), p.1393-1402 |
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Sprache: | eng |
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Zusammenfassung: | About one-third of the more than 300 C2H2 zinc finger proteins of
Drosophila contain a conserved sequence motif, the zinc finger-associated domain (ZAD). Genes that encode ZAD proteins are specific for and expanded in the genomes of insects. Only three ZAD-encoding gene functions are established, and the role of ZAD is unknown. Here we present the crystal structure of the ZAD of Grauzone (ZAD
Grau), a
Drosophila transcription factor that specifically controls the maternal Cdc20-like APC subunit Cortex. ZAD forms an atypical treble-clef-like zinc-coordinating fold. Head-to-tail arrangement of two ZAD
Grau molecules in the crystals suggests dimer formation, an observation supported by crosslinking and dynamic light scattering. The results indicate that ZAD provides a novel protein-protein interaction module that characterizes a large family of insect transcription factors. |
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ISSN: | 0969-2126 1878-4186 |
DOI: | 10.1016/j.str.2003.09.015 |