Genetic variation within and between species is based on recombination of D
NA molecules. Recombination also plays a very important role in the repair
of damaged DNA. Clarity about the mechanism by which recombination occurs i
s of profound interest not only to understand how this process assures the
maintenance of genome integrity and at the same time is the driving force o
f evolution, but also for its application in biotechnology. The isolation o
f genes involved in recombination and the elucidation of the role of many o
f the corresponding gene products in Escherichia coli and Saccharomyces cer
evisiae has formed the basis for comparative analysis in other, more comple
x eukaryotic systems. The identification of homologous genes from different
organisms, including plants, suggests a conservation of the general mechan
isms of recombination.
Transgenes introduced in an organism may be incorporated in the genome by e
ither homologous or nonhomologous recombination (end joining). The preferre
d pathway differs strongly between organisms. In plants there is a preferen
ce for random integration of the introduced DNA by nonhomologous recombinat
ion, which might lead to the accidental inactivation of important genes and
to variable and unpredictable expression of the transgene itself. Therefor
e, there is an urgent need for the development and improvement of technique
s for the directed integration of transgenes at specific locations in the g
enome. The integration of transgenes by homologous recombination would allo
w specific modification or disruption of endogenous genes, providing a tool
for more detailed analysis of gene function. In combination with the recen
t introduction of site-specific recombination systems from E. coil or yeast
into plants, this may lead to the development of versatile systems for mod
ification of the plant genome.