Functional Analysis of the ZAG2 Promoter from Maize in Transgenic Tobaccos

Abstract

AbstractThe function of the 3 040 bp sequence at the upstream translation starting site (ATG) of the ZAG2 gene, isolated from the maize genome, was studied. The sequence analysis showed that the sequence contained a typical class C MADS-box gene regulatory element. The 5′ UTR region of the gene contains a 1 299-bp intron that might have important regulatory functions. To study the sequence function, deletion derivatives of promoter-reporter (uidA) gene fusions were generated and transformed into tobaccos. The GUS staining and fluorescence quantification results showed that the GUS activity was detected only in the third and fourth whorl floral organs of the transgenic tobaccos under driving the promoter including the first intron, while detected in all the organs and was stronger under driving the promoter without the first intron. However, the GUS activity was just detected in one whorl of the fourth or third floral organs under driving of the 35S promoter. These results suggested that the first intron of the ZAG2 gene contains functional regulatory elements, which turned out to be important for gene expression in the heterologous systems. Moreover, the GUS activity was decreased when the reporter gene driven by the promoters with 5′-deletions, respectively, from −1 606 to −951 and −951 to-426 nts, which indicates that positive regulatory elements are present in these two sequence stretches.