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Two negative cis-regulatory regions involved in fruit-specific promoter activity from watermelon (Citrullus vulgaris S.)

机译:西瓜(Citrullus vulgaris S.)的果实特异性启动子活性中涉及两个负的顺式调控区

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摘要

A 1.8 kb 5′-flanking region of the large subunit of ADP-glucose pyrophosphorylase, isolated from watermelon (Citrullus vulgaris S.), has fruit-specific promoter activity in transgenic tomato plants. Two negative regulatory regions, from –986 to –959 and from –472 to –424, were identified in this promoter region by fine deletion analyses. Removal of both regions led to constitutive expression in epidermal cells. Gain-of-function experiments showed that these two regions were sufficient to inhibit RFP (red fluorescent protein) expression in transformed epidermal cells when fused to the cauliflower mosaic virus (CaMV) 35S minimal promoter. Gel mobility shift experiments demonstrated the presence of leaf nuclear factors that interact with these two elements. A TCCAAAA motif was identified in these two regions, as well as one in the reverse orientation, which was confirmed to be a novel specific cis-element. A quantitative β-glucuronidase (GUS) activity assay of stable transgenic tomato plants showed that the activities of chimeric promoters harbouring only one of the two cis-elements, or both, were ∼10-fold higher in fruits than in leaves. These data confirm that the TCCAAAA motif functions as a fruit-specific element by inhibiting gene expression in leaves.
机译:从西瓜(Citrullus vulgaris S.)分离出的ADP-葡萄糖焦磷酸化酶大亚基的1.8 kb 5'侧翼区域在转基因番茄植株中具有果实特异性启动子活性。通过精细缺失分析在该启动子区域中鉴定了两个负调控区,从–986至–959和从–472至–424。两个区域的去除导致在表皮细胞中组成型表达。功能获得的实验表明,与花椰菜花叶病毒(CaMV)35S最小启动子融合时,这两个区域足以抑制转化表皮细胞中的RFP(红色荧光蛋白)表达。凝胶迁移率迁移实验证明存在与这两个元素相互作用的叶核因子。在这两个区域以及反向的一个区域都鉴定出了TCCAAAA基序,这被证实是一种新颖的特异性顺式元件。稳定的转基因番茄植物的定量β-葡萄糖醛酸苷酶(GUS)活性分析表明,仅携带两个顺式元件之一或两者的嵌合启动子的活性比果实高约10倍。这些数据证实了TCCAAAA基序通过抑制叶子中的基因表达而充当了果实特异性元件。

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