Efficient LEC2 activation of OLEOSIN expression requires two neighboring RY elements on its promoter.

NanYing Che, Yang Yang, YanDong Li, LiLi Wang, Ping Huang, Yin Gao, ChengCai An
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引用次数: 20

Abstract

As the main structural protein of oil body, OLEOSIN is highly expressed only during seed development. OLEOSIN promoter is a very useful tool for seed-specific gene engineering and seed bioreactor designing. The B3 domain transcription factor leafy cotyledon2 (LEC2) plays an important role in regulating seed development and seed-specific gene expression. Here, we first report how seed-specific B3 domain transcription factor leafy cotyledon2 (LEC2) efficiently activates OLEOSIN expression. The central promoter region of OLEOSIN, responsible for seed specificity and LEC2 activation, was determined by 5'-deletion analysis. Binding experiments in yeast cells and electrophoretic mobility shift assays showed that LEC2 specifically bound to two conserved RY elements in this region. In transient expression assays, mutation in either RY element dramatically reduced LEC2 activation of OLEOSIN promoter activity, while double mutation abolished it. Analysis of the distribution of RY elements in seed-specific genes activated by LEC2 also supported the idea that genes containing neighboring RY elements responded strongly to LEC2 activation. Therefore, we conclude that two neighboring RY elements are essential for efficient LEC2 activation of OLEOSIN expression. These findings will help us better utilize seed-specific promoter activity.

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高效的LEC2激活OLEOSIN表达需要两个相邻的RY元件在其启动子上。
作为油体的主要结构蛋白,OLEOSIN仅在种子发育过程中高表达。油红启动子是种子特异性基因工程和种子生物反应器设计的重要工具。B3结构域转录因子叶子叶don2 (B3 domain transcription factor leafy cotyledon2, LEC2)在调控种子发育和种子特异性基因表达中起重要作用。在这里,我们首次报道了种子特异性B3结构域转录因子绿叶子叶don2(绿叶子叶don2)如何有效地激活OLEOSIN的表达。OLEOSIN的中心启动子区域负责种子特异性和LEC2激活,通过5'-缺失分析确定。酵母细胞的结合实验和电泳迁移转移实验表明,LEC2特异性地结合了该区域的两个保守的RY元件。在瞬时表达实验中,任何一个RY元素的突变显著降低了OLEOSIN启动子活性的LEC2激活,而双突变则消除了它。对被LEC2激活的种子特异性基因中RY元件分布的分析也支持了含有邻近RY元件的基因对LEC2激活反应强烈的观点。因此,我们得出结论,两个相邻的RY元件对于高效激活OLEOSIN表达的LEC2是必不可少的。这些发现将有助于我们更好地利用种子特异性启动子活性。
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