The Brassica napus nuclear gene, AHAS3R, codes for a mutant chloroplas
t enzyme acetohydroxyacid synthase (AHAS, EC 4.1.3.18) that is resista
nt to inhibition by the sulfonylurea herbicide, chlorsulfuron. It was
introduced into Nicotiana tabacum under control of the cauliflower mos
aic virus 35S promoter and leader sequences. The relative mRNA levels
of the AHAS3R gene and the resident tobacco AHAS genes, SURA and SURB,
were determined by RNAase protection assays. The AHAS3R mRNA level va
ried by more than 6-fold among different transformants, depending on t
he position of insertion and on gene dosage. The expression level was
generally consistant with the percentage of AHAS activity that was chl
orsulfuron-resistant. In contrast, the specific activity of AHAS, whic
h includes the resident tobacco AHAS and introduced AHAS3R activities,
was shown to be independant of AHAS3R gene dosage, mRNA level and pro
portion of chlorsulfuron-resistant enzyme activity. These observations
reveal the presence of a post-transcriptional mechanism that governs
the total amount of AHAS activity in the transgenic plants. When AHAS3
R mRNA levels were at their highest, SURA and SURB activities appeared
to be completely replaced by AHAS3R activity.