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Microinjection - Another possible delivery system might involve the direct injection of foreign DNA into plant cells using minute needles.

Microinjection of DNA into the nuclei of isolated protoplasts could be an efficient means of gene transfer. One good example is alfalfa.

As a technique, microinjection has the following merits:

(1) fairly high transformation efficiencies,

(2) minimal somaclonal variation because of avoidance of the cell culture phase following egg cell injection, and

(3) high efficiency of transfer of chromosomes and organelles. This is now being exploited for the transformation of gametes and the transfer of chromosomes and organelles between plant species.

The microinjection technique has been routinely applied in mice. The mouse egg is first immobilized by applying mild suction.

Many copies of the gene of interest are then injected through the fine sharp end of a narrow microneedle. Scientists have obtained some promising preliminary results using this method.

The germ cells of the rye plant are located in a flower cluster known as an inflorescence.

Materials injected into the inflorescence can penetrate the developing germ cells.

For example, injection of the chemicals caffeine and colchicine penetrate the cells and produce developmental abnormalities in them.

To test whether DNA would also penetrate the cells, de la Pena (1987) injected rye inflorescences with DNA plasmids consisting primarily of a gene coding for resistance to the antibiotic kanamycin.

The seeds eventually produced were then screened for kanamycin resistance by germinating them in the presence of the antibiotic.

The first batch of about 3,000 seeds, derived from approximately 70 injected rye inflorescences, produced three seedlings that contained and expressed the kanamycin resistance gene.

Although this initial success should be considered preliminary and in need of replication, the result indicates that simple methods can probably be developed for introducing foreign genes into cereal plants.