The present review summarizes the factors involved in controlling the proce
ss of oak somatic embryogenesis as a method for vegetative plant propagatio
n and includes also data on artificial seed production, cryopreservation an
d transformation. One major limitation. the inability to initiate embryogen
ic cultures from mature trees, has: been recently overcome. Leaves from sel
ected cork oak trees with an age of 50 yr and more have been used to, initi
ate somatic embryogenesis (SE) with a frequency of up to 20%. These finding
s offer encouraging prospects for cloning proven superior plant material an
d to integrate this propagation system into, tree improvement programs. Onc
e thr process of SE has been initiated, the multiplication cycle proceeds v
ia secondary embryogenesis. which can bt maintained indefinitely. Problems
are reported by the formation of anomalous embryos. The mutability of somat
ic. embryogenic cell lines of various oak species has been monitored by flo
w cytometry and molecular markers. No somaclonal variation was detected app
lying random amplified polymorphic DNA (RAPD) or amplified fragment length
polymorphism (AFLP) markers. whereas DNA-content measurements via now cytom
etry revealed tetraploidy in some cell lines after several years of continu
ous subculture. Maturation and low germination frequencies are the main bot
tlenecks for a broader use of this technique. Recently attention has been o
n embryo quality and parameters for conversion capacity such as high endoge
nous cytokinin level and low abscisic a id (ABA) level. Although oak is pro
bably the species that is the most well-developed system for a broadleaved
forest tree, data on growth performances of somatic embryo-derived plants a
re rare.