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
Hauptverfasser: Jauch, Ralf, Bourenkov, Gleb P, Chung, Ho-Ryun, Urlaub, Henning, Reidt, Ulrich, Jäckle, Herbert, Wahl, Markus C
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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.
ISSN:0969-2126
1878-4186
DOI:10.1016/j.str.2003.09.015