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A maize α-zein promoter drives an endosperm-specific expression of transgene in rice

机译:玉米α-玉米醇溶蛋白启动子驱动水稻的胚乳特异性转基因表达

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摘要

An alpha-zein promoter isolated from maize containing P-box, E motif sequence TGTAAAGT, opaque-2 box and TATA box was studied for its tissue-specific expression in rice. A 1,098 bp promoter region of alpha-zein gene, fused to the upstream of gusA reporter gene was used for transforming rice immature embryos (ASD 16 or IR 64) via the particle bombardment-mediated method. PCR analysis of putative transformants demonstrated the presence of transgenes (the zein promoter, gusA and hpt). Nineteen out of 37 and two out of five events generated from ASD 16 and IR 64 were found to be GUS-positive. A histological staining analysis performed on sections of mature T1 seeds revealed that the GUS expression was limited to the endosperm and not to the pericarp or the endothelial region. GUS expression was observed only in the following seed development stages : milky (14–15 DAF), soft dough (17–18 DAF), hard dough (20–23 DAF), and mature stages (28–30 DAF) of zein-gusA transformed (T0) plants. On the contrary a constitutive expression of GUS was evident in CaMV35S-gusA plants. PCR and Southern blotting analyses on T1 plants demonstrated a stable integration and inheritance of transgene in the subsequent T1 generation. GUS assay on T2 seeds revealed that the expression of gusA gene driven by alpha-zein promoter was stable and tissue-specific over two generations. Results suggest that this alpha-zein promoter could serve as an alternative promoter to drive endosperm-specific expression of transgenes in rice and other cereal transformation experiments.
机译:研究了从玉米中分离得到的α-玉米醇溶蛋白启动子,该启动子在水稻中具有组织特异性表达,所述启动子包含P-box,E基序序列TGTAAAAT,opaque-2box和TATA box。融合到gusA报告基因上游的α-玉米醇溶蛋白基因的1,098bp启动子区域用于通过粒子轰击介导的方法转化水稻未成熟胚(ASD 16或IR 64)。推定的转化子的PCR分析表明存在转基因(玉米醇溶蛋白启动子,gusA和hpt)。从ASD 16和IR 64产生的事件中,有37个事件中有19个和5个事件中有2个是GUS阳性的。对成熟的T1种子的切片进行的组织学染色分析表明,GUS表达仅限于胚乳,而不限于果皮或内皮区域。仅在以下种子发育阶段观察到GUS表达:玉米醇溶蛋白的乳白色(14-15 DAF),软面团(17-18 DAF),硬面团(20-23 DAF)和成熟阶段(28-30 DAF)。 gusA转化(T0)植物。相反,在CaMV35S-gusA植物中GUS的组成型表达是明显的。对T1植物的PCR和Southern印迹分析表明,转基因在随后的T1世代中稳定整合并遗传。在T2种子上进行GUS分析表明,α-玉米醇溶蛋白启动子驱动的gusA基因的表达在两代内稳定且具有组织特异性。结果表明,这种α-玉米醇溶蛋白启动子可以作为替代启动子,在水稻和其他谷物转化实验中驱动胚乳特异性转基因表达。

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