The genetic investigation of fungi has been extended substantially by
DNA-mediated transformation, providing a supplement to more convention
al generic approaches based upon sexual and parasexual processes. Init
ial transformation studies with the yeast Saccharomyces cerevisiae pro
vided the model for transformation systems in other fungi with regard
to methodology, vector construction and selection strategies. There ar
e, however, certain differences between S. cerevisiae and filamentous
fungi with regard to type of genomic insertion and the availability of
shuttle vectors. Single-site linked insertions are common in yeast du
e to the high level of homology required for recombination between vec
tored and genomic sequences, whereas mycelial fungi often show a high
frequency of heterologous and unlinked insertions, often in the form o
f random and multiple-site integrations. While extrachromosomally-main
tained or replicative vectors are readily available for use with yeast
s, such vectors have been difficult to construct for use with filament
ous fungi. The development of vectors for replicative transformation w
ith these fungi awaits further study. It is proposed that replicative
vectors may be inherently less efficient for use with mycelial fungi r
elative to yeasts, since the mycelium, as an extended and semicontinuo
us network of cells, may delimit an adequate diffusion of the vector c
arrying the selectable gene, thus leading to a high frequency of abort
ive or unstable transformants.