We have isolated a gene, hmgl, for 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMCR) from Camptotheca acuminata, aChinese tree that produces the anti-cancer monoterpenoid indole alkaloid camptothecin (CPT). HMCR supplies mevalonate for the synthesis of the terpenoid component of CPT as well as for the formation of many other primary and secondary metabolites. In Camptotheca, hmgl transcripts were detected only in young seedlings and not in vegetative organs of older plants. Regulation of the hmgl promoter was studied in transgenic tobacco using three translational fusions (-1678, -1 107, -165) with the B-glucuronidase (GUS) reporter gene. Histochemical analysis of plants containing each of the three promoter fusions showed similar developmental and spatial expression patterns. In vegetative tissues, CUS staining was localized to the epidermis of young leaves and stems, particularly in glandular trichomes. Roots showed intense staining in the cortical tissues in the elongation zone and light staining in the cortex of mature roots. hmgl::CUS expression was also observed in sepals, petals, pistils, and stamens of developing flowers, with darkest staining in the ovary wall, ovules, stigmas, and pollen. Leaf discs from plants containing each of the translational fusions showed a 15-to 20-fold wound induction of hmgl::CUS expression over 72 h; however, this increase in CUS activity was completely suppressed by treatment with methyl jasmonate. Taken together, these data show that a 165-bp fragment of Camptotheca hmgl promoter is sufficient to confer developmental regulation as well as wound induction and methyl jasmonate suppression of GUS expression in transgenic tobacco.