Hwang Yong-Sic, Ciceri Pietro, Parsons Ronald L, Moose Stephen P, Schmidt Robert J, Huang Ning
Ventria Bioscience, 4110 N. Freeway Blvd, Sacramento, CA 95834, USA.
Plant Cell Physiol. 2004 Oct;45(10):1509-18. doi: 10.1093/pcp/pch173.
A transient expression assay system was employed to investigate the possible use of the maize Opaque 2 (O2) and prolamin box binding factor (PBF) proteins as transcriptional activators of rice and wheat storage protein gene promoters. When assayed in developing rice endosperm cells, either O2 or PBF alone could increase transcription from the promoter of the rice glutelin gene, Gt1. However, mutant forms of O2 and PBF that are defective in DNA binding could not. Co-transfection with both transcriptional activators resulted in an additive increase in transactivation of the Gt1 promoter. Co-bombardment of a Gt1::GUS construct with plasmids expressing the DNA binding domains of O2 and PBF in antisense orientation resulted in a decrease of GUS expression below background levels. Similar stimulatory and additive effects of O2 and PBF could be observed on the promoters from other storage protein genes including rice globulin (Glb), prolamins (RP6 and PG5a) and a wheat glutenin (Bx7). However, responsiveness of the promoters from non-storage protein genes like rice actin and CaMV 35S to O2 and PBF was insignificant. Our results indicate that the maize O2 and PBF proteins can act singly or additively as effective stimulators of heterologous storage protein promoters in developing rice endosperm cells. These data support the use of well-characterized transcription factors from maize as an effective means of increasing the expression level of recombinant proteins in developing rice seeds.
采用瞬时表达分析系统,研究玉米不透明2(O2)蛋白和醇溶蛋白盒结合因子(PBF)作为水稻和小麦贮藏蛋白基因启动子转录激活因子的潜在用途。在发育中的水稻胚乳细胞中进行检测时,单独的O2或PBF均可增加水稻谷蛋白基因Gt1启动子的转录。然而,DNA结合有缺陷的O2和PBF突变体形式则不能。两种转录激活因子共转染导致Gt1启动子的反式激活呈累加增加。将Gt1::GUS构建体与以反义方向表达O2和PBF DNA结合结构域的质粒共轰击,导致GUS表达降至背景水平以下。在包括水稻球蛋白(Glb)、醇溶蛋白(RP6和PG5a)和小麦谷蛋白(Bx7)在内的其他贮藏蛋白基因的启动子上,也可观察到O2和PBF类似的刺激和累加效应。然而,水稻肌动蛋白和花椰菜花叶病毒35S等非贮藏蛋白基因的启动子对O2和PBF的反应不明显。我们的结果表明,玉米O2和PBF蛋白可单独或累加地作为发育中水稻胚乳细胞中异源贮藏蛋白启动子的有效刺激因子。这些数据支持利用已充分表征的玉米转录因子作为提高重组蛋白在发育中的水稻种子中表达水平的有效手段。