Cloning of an ovule specific promoter from <i style="">Arabidopsis thaliana </i>and expression of β-glucuronidase

Abstract

Tissue specific expression of transgenes in plant species has several advantages over constitutive expression. Identification of ovule specific promoters would be useful in genetic engineering of plants with a variety of desirable traits such as genetically engineered parthenocarpy, female sterile plants or seedless fruits. Relative inaccessibility and difficulty in harvesting adequate amounts of tissue at known developmental stages has impeded the progress in cloning of promoters involved in ovule development. In the present study an ovule specific promoter was cloned from <i style="">Arabidopsis AGL11</i>^Ψ<i style=""> </i>gene and used to express GUS (β-<i style="">glucuronidase</i>) gene in transgenic <i style="">Arabidopsis</i>. Histochemical staining of GUS appeared in the center of young ovary (ovules), but no detectable GUS<i style=""> </i>activity was observed in vegetative plant tissues, sepals, petals and androecium. <i style="">AGL11</i> gene promoter can be useful to modify the developmental path of plants by expressing either plant hormones or lethal genes for agronomic purpose.<b style=""> </b>