A novel DNA-binding domain in theShrunken initiator-binding protein (IBP1)

Abstract
South-western screening of λgt11 expression library with a fragment of theShrunken promoter containing the initiator element resulted in cloning of a novel maize gene. The encoded initiator-binding protein (IBP1) interacts at the transcription start site of theShrunken promoter. Analysis of the 680 amino acid (aa) long polypeptide revealed a novel bipartite DNA-binding domain at the carboxyl terminus. In its amino-terminal part, it is weakly related toMyb R-repeats but the following basic region is also essential for DNA binding. A region of similarity to the conserved 2.1 and 2.2. motifs in bacterial σ-factors is located close to the IBP1 amino terminus. Two putative nuclear localization signals are compatible with the presence of antigenically related polypeptides in nuclear protein extracts. TheIBP1 gene was mapped to the long arm of chromosome 9 (9L095); a second highly related geneIBP2 is located on the short arm of chromosome 1 (1S014). Both genes encode proteins sharing 93% similarity and are transcribed with similar activity in different plant organs. A small 82 nucleotide intron in theIBP2 transcript is found unspliced to a variable degree in different tissues. Translation of this incompletely processed transcript would result in a truncated amino-terminal polypeptide lacking the DNA-binding domain.