Abstract: Described are plants not naturally capable of reducing dihydrokaempferol and containing a DNA sequence inserted according to recombinant DNA techniques which DNA sequence encodes a protein with the enzymatic activity of a dihydroflavonol 4-reductase (DFR) with extended substrate specificity for dihydrokaempferol. Furthermore, methods for the production of said plants, recombinant vectors and the use of said plants for the breeding of plants and parts of plants with modified flower colour are described.

Abstract: Expression constructs are provided employing a plant EF-1.alpha. promote which allows for elevated expression in rapidly dividing cells. Sequences from the gene and untranslated regions associated with the gene may be employed in an antisense construct to reduce growth rate. The promoter finds particular use in protecting rapidly dividing tissue and tender shoots from a wide variety of environmentally induced stress conditions.

Abstract: Process for introducing foreign DNA into the genome of plants by infecting plants or explantates thereof or plant protoplasts or by incubating plant protoplasts with Agrobacterium, in which Agrobacteria are used, which contain one or more T-regions and a Vir-region from the Ti-plasmid of Agrobacterium in their genetic material and/or one or more T-regions comprising an artificial T-region which consists of each DNA desired, flanked by border sequences as present in the wild type T-region of Agrobacterium or sequences being functionally analogous thereto.

Abstract: Fragments of the 35S promoter of cauliflower mosaic virus are disclosed which exhibit selective expression of chimeric plant genes in plant tissue. Promoter fragment A exhibits selective expression in root tissue and the radical of the seed. Promoter fragment B exhibits constitutive expression in plant tissue other than root tissue.

Abstract: DNA sequence of S-genes which encode S-proteins and control the self-incompatibility reaction in gametophytic self-incompatible plants have been identified. The DNA sequence encoding several S-proteins of N. alata and their attendant signal sequences are specifically provided. Regulatory sequences which direct expression of the S-genes in reproduction tissue of self-incompatible plants have also been identified. A method for the identification and isolation of cDNA and genomic DNA coding sequences of the S-genes is described.