ZM13 is a pollen-specific maize gene which is expressed in the late st
ages of pollen development. We wished to utilize the ZM13 promoter to
examine the expression of a synthetic green fluorescent protein (SGFP)
in germinating pollen. The usefulness of the SGFP expression product
is that its appearance and distribution can be monitored non-destructi
vely in vivo. A plasmid containing the SGFP coding region under the co
ntrol of the ZM13 promoter was constructed and then transiently transf
ormed into pollen of Tradescantia paludosa and Nicotiana tabacum by th
e use of microprojectile bombardment. The expression of the green fluo
rescent protein was analyzed by fluorescence microscopy using a fluore
scein filter. Expression began about 3 h post-bombardment, and all par
ts of the pollen grain and tube fluoresced. High levels of fluorescenc
e were observed for several days following treatment.