Chromatin structure of transferred genes in transgenic plants

Abstract

AbstractThe chromatin structure of foreign genes in transgenic tobacco plants was investigated by digestion of nuclei with DNase I and micrococcal nuclease, respectively, followed by restriction and Southern analysis of the digestion products. The results were compared to the differential expression of the different transgenes. Two model systems were used: plants harbouring vector DNA derived from the disarmed vector pGV 3850 and plants harbouring the light‐regulated and organ‐specifically expressed potato ST‐LS1 gene and the cotransferred ncpaline synthase (nos) reporter gene. Our results show that transferred genes are located in DNase l‐sensitive domains in all transformants. Slight variations of DNase l‐sensitivity of the transferred ST‐LS1 constructs in different transformants neither reflected the between‐transformant variability of expression nor the organ‐specific activity of the transgenes. A deletion event was found responsible for silencing the ST‐LS1 gene but not the nos gene in one of the transformants. Whereas no DNase l‐hypersensitive sites were found within the 3850‐T‐DNA and the ST‐LS1 gene, one prominent site was mapped to the nos promoter within the ST‐LS1 construct in all transformants. Digestion of chromatin harbouring 3850‐T‐DNA with micrococcal nuclease resulted in a blurred nucleosomal pattern as compared to nucleolar and bulk chromatin, the extent of blurring being independent of the expression of transferred genes. The present results favour the “permissive domain” hypothesis which capitalizes on the chromatin surrounding the integration site as the determining factor for the chromatin structure of incoming alien genes. However, between‐transformant variability of expression is not reflected by differential sensitivity to DNase I. Hence, other factors than chromatin structure must be involved in creating “position effects”.