To compare the transformation effects of two different forms （cDNA in monocotyledonous plant Echinochloa crusgalli, DNA in monocotyledonous plant Zea mays） of phosphoenolpyruvate carboxylase （PEPC） gene （Ppc） on...To compare the transformation effects of two different forms （cDNA in monocotyledonous plant Echinochloa crusgalli, DNA in monocotyledonous plant Zea mays） of phosphoenolpyruvate carboxylase （PEPC） gene （Ppc） on the growth of transgenic dicotyledonous plant, Agrobacterium-mediated transformation of Ppc genes into Nicotiana tabacum were carried out. Transgenic leaf plates and differentiated seedling leaves were verified by GUS histochemistry, PCR, and RT-PCR. Results showed that transgenic N. tabacum with Ppc-cDNA of E. crusgalli had relatively strong differentiation ability. However, N. tabacum after transformation of complete DNA sequence of Ppc genes in Z mays had relatively poor ability of growth. The differentiated green seedlings had the phenomenon of yellowing; and photosynthesis ability of leaves was poor. This might be caused by the misidentification and wrong splicing in transcription. This indicated that the expression rate of monocotyledonous complete DNA might be reduced in the monocotyledonous cells with relatively far genetic distances. Detection results of showed that Pn in most transgenic N. tabacum with Ppc-cDNA of E. crusgalli was was higher than that in control, which preliminarily proved that PEPC of monocotyledonous plant E. crusgalli had certain regulatory effects on photosynthesis of N. tabacum.展开更多
基金Supported by the Innovation Project of Chinese Academy of Agricultural Sciences~~
文摘To compare the transformation effects of two different forms （cDNA in monocotyledonous plant Echinochloa crusgalli, DNA in monocotyledonous plant Zea mays） of phosphoenolpyruvate carboxylase （PEPC） gene （Ppc） on the growth of transgenic dicotyledonous plant, Agrobacterium-mediated transformation of Ppc genes into Nicotiana tabacum were carried out. Transgenic leaf plates and differentiated seedling leaves were verified by GUS histochemistry, PCR, and RT-PCR. Results showed that transgenic N. tabacum with Ppc-cDNA of E. crusgalli had relatively strong differentiation ability. However, N. tabacum after transformation of complete DNA sequence of Ppc genes in Z mays had relatively poor ability of growth. The differentiated green seedlings had the phenomenon of yellowing; and photosynthesis ability of leaves was poor. This might be caused by the misidentification and wrong splicing in transcription. This indicated that the expression rate of monocotyledonous complete DNA might be reduced in the monocotyledonous cells with relatively far genetic distances. Detection results of showed that Pn in most transgenic N. tabacum with Ppc-cDNA of E. crusgalli was was higher than that in control, which preliminarily proved that PEPC of monocotyledonous plant E. crusgalli had certain regulatory effects on photosynthesis of N. tabacum.
