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Published online 12 March 2004

Nucleic Acids Research, 2004, Vol. 32, No. 5 1710-1720
© 2004 Oxford University Press

The maize ID1 flowering time regulator is a zinc finger protein with novel DNA binding properties

Akiko Kozaki1, Sarah Hake1 and Joseph Colasanti*,1,2

1 Department of Plant and Microbial Biology, University of California, Berkeley, and the Plant Gene Expression Center, Albany, CA 94720, USA and 2 Department of Molecular Biology and Genetics, University of Guelph, Guelph, Ontario N1G 2W1, Canada

*To whom correspondence should be addressed. Tel: +1 519 824 4120 ext. 58052; Fax: +1 519 837 2075; Email: jcolasan{at}uoguelph.ca

The INDETERMINATE protein, ID1, plays a key role in regulating the transition to flowering in maize. ID1 is the founding member of a plant-specific zinc finger protein family that is defined by a highly conserved amino sequence called the ID domain. The ID domain includes a cluster of three different types of zinc fingers separated from a fourth C2H2 finger by a long spacer; ID1 is distinct from other ID domain proteins by having a much longer spacer. In vitro DNA selection and amplification binding assays and DNA binding experiments showed that ID1 binds selectively to an 11 bp consensus motif via the ID domain. Unexpectedly, site-directed mutagenesis of the ID1 protein showed that zinc fingers located at each end of the ID domain are not required for binding to the consensus motif despite the fact that one of these zinc fingers is a canonical C2H2 DNA binding domain. In addition, an ID1 in vitro deletion mutant that lacks the extra spacer between zinc fingers binds the same 11 bp motif as normal ID1, suggesting that all ID domain-containing proteins recognize the same DNA target sequence. Our results demonstrate that maize ID1 and ID domain proteins have novel zinc finger configurations with unique DNA binding properties.


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