Although Ustilago maydis is readily amenable to molecular genetic expe
rimentation, few antibiotic-resistance markers are available for DNA-m
ediated transformation. This poses constraints on experiments involvin
g targeted gene disruption and complementation. To address this proble
m, we constructed vectors using one of three additional genes as domin
ant selectable markers for transformation. Two genes, sat-1 (encoding
streptothricin acetyltransferase) and Sh-ble (encoding a phleomycin-re
sistance polypeptide), are of bacterial origin and have been engineere
d for expression in Ustilago sp. The third gene encodes an allele of U
. maydis beta-tubulin that confers resistance to the fungicide benomyl
.