Isolation and identification of a vegetative organ-specific promoter from maize.

To avoid the unregulated overexpression of the exogenous genes, specific or inducible expression is necessary for some exogenous genes in transgenic plants. But little is known about organ- or tissue-specific promoters in maize. In the present study, the expression of a maize pentatricopeptide repeat (PPR) protein encoding gene, , was analyzed by RNA-sequencing data and confirmed by quantitative real time PCR. The results showed that the gene specifically expressed in vegetative organs. Consequently, a 1830 bp sequence upstream of the start codon of the promoter for gene was isolated from maize genome ( ). To validate whether the promoter possesses the vegetative organ-specificity, the full-length and three 5'-end deletion fragments of of different length (1387, 437, and 146 bp) were fused with glucuronidase (GUS) gene to generate constructs and transformed into tobacco. The transient expression and fluorometric GUS assay in transgenic tobacco showed that all promoter could drive the expression of the gene, the - 437 to - 146 bp region possessed some crucial elements for root-specific expression, and the shortest and optimal sequence to maintain transcription activity was 146 and 437 bp in length, respectively. These results indicate that the promoter of the gene is a vegetative organ-specific promoter and will be useful in transgenic modification of commercial crops for moderate specific expression after further evaluation in monocotyledons.