Insertional mutagenesis in Arabidopsis can be conveniently accomplished either by Agrobacterium mediated TDNA transformation, or by transposable element mobilization. Recent advances have made T-DNA transformation one of the most efficient methods to generate large numbers of insertions in the Arabidopsis genome (1-3). Typically, several hundred independent T-DNA insertions can be generated per transformed plant. This is many more insertions than in most transposon schemes, but despite the labor involved, transposons have some important advantages: