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A promoter of the PNZIP(Pharbitis nil leucine zipper)gene(1.459 kb)was cloned from Pharbitis nil and fused to the GUS(b-glucuronidase)and Bacillus thuringiensis endotoxin(Cry9C)genes.Several transgenic PNZIP::GUS and PNZIP::Cry9C cotton lines were developed by Agrobacterium-mediated transformation.Strong GUS staining was detected in the green tissues of the transgenic PNZIP::GUS cotton plants.In contrast,GUS staining in the reproductive structures such as petals,anther,and immature seeds of PNZIP::GUS cotton was very faint.Two transgenic PNZIP::Cry9C lines and one transgenic cauliflower mosaic virus(Ca MV)35S::Cry9C line were selected for enzyme-linked immunosorbent assay(ELISA)and insect bioassays.Expression of the Cry9C protein in the 35S::Cry9C line maintained a high level in most tissues ranging from24.6 to 45.5μg g~(-1) fresh weight.In green tissues such as the leaves,boll rinds,and bracts of the PNZIP::Cry9C line,the Cry9C protein accumulated up to 50.2,39.7,and 48.3μg g~(-1) fresh weight respectively.In contrast,seeds of the PNZIP::Cry9C line(PZ1.3)accumulated only 0.26μg g~(-1) fresh weight of the Cry9C protein,which was 100 times lower than that recorded for the seeds of the Ca MV 35S::Cry9C line.The insect bioassay showed that the transgenic PNZIP::Cry9C cotton plant exhibited strong resistance to both the cotton bollworm and the pink bollworm.The PNZIP promoter could effectively drive Bt toxin expression in green tissues of cotton and lower accumulated levels of the Bt protein in seeds.These features should allay public concerns about the safety of transgenic foods.We propose the future utility of PNZIP as an economical,environmentally friendly promoter in cotton biotechnology.
A promoter of the PNZIP (Pharbitis nil leucine zipper) gene (1.459 kb) was cloned from Pharbitis nil and fused to the GUS (b-glucuronidase) and Bacillus thuringiensis endotoxin (Cry9C) genes.Several transgenic PNZIP :: GUS and PNZIP :: Cry9C cotton lines were developed by Agrobacterium-mediated transformation. Strong GUS staining was detected in the green tissues of the transgenic PNZIP :: GUS cotton plants. In contrast, GUS staining in the reproductive structures such as petals, anther, and immature seeds of PNZIP :: GUS cotton was very faint. Two transgenic PNZIP :: Cry9C lines and one transgenic cauliflower mosaic virus (Ca MV) 35S :: Cry9C line were selected for enzyme-linked immunosorbent assay (ELISA) and insect bioassays. Expression of the Cry9C protein in the 35S :: Cry9C line maintained a high level in most tissues ranging from 24.6 to 45.5 μg g -1 fresh weight. In green kits such as the leaves, boll rinds, and bracts of the PNZIP :: Cry9C line , the Cry9C protein accumulated up to 50.2, 39.7, and 48.3 μg g ~ (-1) f resh weight respectively.In contrast, seeds of the PNZIP :: Cry9C line (PZ1.3) accumulated only 0.26 μg g -1 fresh weight of the Cry9C protein, which was 100 times lower than that recorded for the seeds of the Ca MV 35S :: Cry9C line.The insect bioassay showed that the transgenic PNZIP :: Cry9C cotton plant showed strong resistance to both the cotton bollworm and the pink bollworm.The PNZIP promoter could effectively drive Bt toxin expression in green tissues of cotton and lower accumulated levels of the Bt protein in seeds. these features should allay public concerns about the safety of transgenic foods.We propose the future utility of PNZIP as an economical, environmentally friendly promoter in cotton biotechnology.