Many systems have been developed for the removal of a selection marker in o
rder to generate marker-free transgenic plants. These systems consist of (1
) a site-specific recombination system (Cre/lox) or a phage-attachment regi
on (attP) to remove the selectable marker gene and (2) a transposable eleme
nt system (Ac) or a cotransformation system to segregate the gene of intere
st from the selectable marker gene. Overall, the process is more time-consu
ming than conventional transformation methods because two rounds of transfo
rmation - two steps of regeneration or sexual crossings - are required to o
btain the desired transgenic plants. Recently, removal systems combined wit
h a positive marker, denoted as MAT vectors, have been developed to save ti
me and effort by generating marker-free transgenic plants through a single-
step transformation. We summarize here the transformation procedures using
these systems and discuss their feasibility for practical use.