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Constitutive promoters available for transgene expression instead of CaMV 35S RNA promoter: Arabidopsis promoters of tryptophan synthase protein #beta# subunit and phytochrome B

机译:可用于转基因表达的组成型启动子,而不是CaMV 35S RNA启动子:色氨酸合酶蛋白#beta#亚基和植物色素B的拟南芥启动子

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摘要

To search for strong promoters that confer constitutive expression of transgenes, we evaluated the promoters of an Arabidopsis tryptophan synthase protein #beta# subunit gene (PTSB1) and a phytochrome B gene (PPHYB) as alternatives to the 35S RNA promoter (P35S) of Cauliflower mosaic virus. Characteristics of the Soybean chrolotic mottle virus promoter (PNCR) were also studied for comparison. In transgenic calli, GUS gene fused with PTSB1, PPHYB and PNCR showed 50 percent or more of the activity ofP35S. To drive the NPTII marker gene, the four promoters were similarly useful. In generated transgenic tobacco plants, both PTSB1 and PPHYB were active in all tissues tested, and superior to P35S in the leaves. The four promoters differed slightly in their tissue - specific expression, but were expressed constitutively, indicating that PTSB1 and PPHYB as well as PNCR are useful as strong, and constitutive promoters as alternatives to P35S for genetic manipulation of plants.
机译:为了寻找能赋予转基因组成型表达的强启动子,我们评估了拟南芥色氨酸合酶蛋白#beta#亚基基因(PTSB1)和植物色素B基因(PPHYB)的启动子,作为花椰菜35S RNA启动子(P35S)的替代物花叶病毒。还研究了大豆色斑驳病毒启动子(PNCR)的特征以进行比较。在转基因愈伤组织中,与PTSB1,PPHYB和PNCR融合的GUS基因显示出P35S活性的50%或更多。为了驱动NPTII标记基因,四个启动子同样有用。在生成的转基因烟草植物中,PTSB1和PPHYB在所有测试的组织中均具有活性,并且在叶片中均优于P35S。这四个启动子在其组织特异性表达上略有不同,但组成性表达,这表明PTSB1和PPHYB以及PNCR可用作强力组成型启动子,作为P35S的替代品用于植物的基因操作。

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