TARGETING TRANSGENE EXPRESSION IN APPLE TREE TISSUES -ROLES FOR HETEROLOGOUS AND HOMOLOGOUS PROMOTERS

Targeting transgene expression to specific cells and tissues is desirable for a number of reasons (Gittins et al., 2000) not least of which is the requirement to reduce perceived risks with GM technology. In fruit crops, where invariably the product is consumed fresh, this assumes unparalleled importance.
To this end, the ability of several heterologous and homologous gene promoters to drive expression of the -glucuronidase (gusA) marker gene in the vegetative tissues of transgenic apple (Malus pumila, Mill.) have and are being tested.
These promoters originally drove expression in leaves (Rubisco, small subunit (SSU), RBCS3C from tomato, SRS1 from soybean), in vascular tissue (rolC, and CoYMV) and in root tissue (extA from Brassica). Homologous promoters from apple were cloned for expression in fruit.
Transgenic lines were produced by Agrobacterium-mediated transformation and the levels of gusA activity in the vegetative tissues of young plants were compared with those using the CaMV 35S promoter to drive expression of the same gene.
Quantitative GUS data were related to the copy number of transgene loci assessed by Southern blotting.
The precise location of GUS activity in each tissue was identified by staining of whole leaves and tissue sections with the chromogenic substrate X-Gluc.
Light-regulation and patterns of expression are recorded in various vegetative tissues of apple.