Grotewold E, Drummond B J, Bowen B, Peterson T
Cold Spring Harbor Laboratory, New York 11724-2212.
Cell. 1994 Feb 11;76(3):543-53. doi: 10.1016/0092-8674(94)90117-1.
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.
玉米P基因决定了玉米粒果皮、玉米穗轴及其他花器官的红色素沉着,自现代遗传学早期以来,它一直是一个重要的模型。我们在此表明,P编码一个识别序列CCT/AACC的Myb同源物,这与脊椎动物Myb蛋白所结合的C/TAACGG形成鲜明对比。P结合并激活3-脱氧类黄酮和紫穗槐二烯生物合成所需的A1基因的转录,但不激活花青素生物合成所需的Bz1基因的转录。同样编码Myb同源物的玉米C1基因,仅在存在由玉米基因R或B编码的碱性螺旋-环-螺旋共激活因子时,才激活A1和Bz1基因。这些结果表明,Myb同源物可通过结合不同的DNA序列、与其他因子的组合相互作用或两者兼而有之,来差异调节基因表达。