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      The myb-homologous P gene controls phlobaphene pigmentation in maize floral organs by directly activating a flavonoid biosynthetic gene subset.

      Cell
      Animals, Base Sequence, Binding Sites, DNA-Binding Proteins, genetics, metabolism, Flavonoids, biosynthesis, Gene Expression Regulation, Genes, Plant, Genes, Regulator, Molecular Sequence Data, Mutagenesis, Oncogene Proteins v-myb, Oncogenes, Pigments, Biological, Plant Proteins, Promoter Regions, Genetic, Retroviridae Proteins, Oncogenic, Sequence Homology, Nucleic Acid, Transcription, Genetic, Vertebrates, Zea mays, physiology

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          Abstract

          The maize P gene, which specifies red pigmentation of the kernel pericarp, cob, and other floral organs, has been an important model since the early days of modern genetics. Here we show that P encodes a Myb homolog that recognizes the sequence CCT/AACC, in sharp contrast with the C/TAACGG bound by vertebrate Myb proteins. P binds to and activates transcription of the A1 gene required for 3-deoxy flavonoid and phlobaphene biosynthesis, but not the Bz1 gene required for anthocyanin biosynthesis. The maize C1 gene, which also encodes a Myb homolog, activates both the A1 and Bz1 genes, but only in the presence of a basic-helix-loop-helix coactivator encoded by the maize genes R or B. These results indicate that Myb homologs can differentially regulate gene expression by binding different DNA sequences, through combinatorial interactions with other factors, or both.

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