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转录因子苯类物质 II 激活 MYB 气味受体 1 启动子,该启动子在特定于芳香型矮牵牛的 MYB 结合位点上。

The transcription factor EMISSION OF BENZENOIDS II activates the MYB ODORANT1 promoter at a MYB binding site specific for fragrant petunias.

机构信息

Department of Plant Physiology, Swammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, The Netherlands.

出版信息

Plant J. 2011 Sep;67(5):917-28. doi: 10.1111/j.1365-313X.2011.04644.x. Epub 2011 Jul 1.

Abstract

Fragrance production in petunia flowers is highly regulated. Two transcription factors, ODORANT1 (ODO1) and EMISSION OF BENZENOIDS II (EOBII) have recently been identified as regulators of the volatile benzenoid/phenylpropanoid pathway in petals. Unlike the non-fragrant Petunia hybrida cultivar R27, the fragrant cultivar Mitchell highly expresses ODO1. Using stable reporter lines, we identified the 1.2-kbp ODO1 promoter from Mitchell that is sufficient for tissue-specific, developmental and rhythmic expression. This promoter fragment can be activated in non-fragrant R27 petals, indicating that the set of trans-acting factors driving ODO1 expression is conserved in these two petunias. Conversely, the 1.2-kbp ODO1 promoter of R27 is much less active in Mitchell petals. Transient transformation of 5' deletion and chimeric Mitchell and R27 ODO1 promoter reporter constructs in petunia petals identified an enhancer region, which is specific for the fragrant Mitchell cultivar and contains a putative MYB binding site (MBS). Mutations in the MBS of the Mitchell promoter decreased overall promoter activity by 50%, highlighting the importance of the enhancer region. We show that EOBII binds and activates the ODO1 promoter via this MBS, establishing a molecular link between these two regulators of floral fragrance biosynthesis in petunia.

摘要

矮牵牛花朵中的香气产生受到高度调控。最近,两个转录因子,气味受体 1(ODO1)和苯丙烷类化合物的排放 II(EOBII),被鉴定为花瓣中挥发性苯丙烷/苯丙氨酸途径的调节剂。与无香味的矮牵牛杂交品种 R27 不同,芳香品种 Mitchell 高度表达 ODO1。使用稳定的报告基因系,我们从 Mitchell 中鉴定出了 1.2kbp 的 ODO1 启动子,该启动子足以进行组织特异性、发育性和节律性表达。这个启动子片段可以在无香味的 R27 花瓣中被激活,表明驱动 ODO1 表达的一组反式作用因子在这两个矮牵牛中是保守的。相反,R27 的 1.2kbp ODO1 启动子在 Mitchell 花瓣中的活性要低得多。在矮牵牛花瓣中瞬时转化 5'缺失和嵌合 Mitchell 和 R27 ODO1 启动子报告基因构建体,确定了一个增强子区域,该区域特异性存在于芳香的 Mitchell 品种中,包含一个假定的 MYB 结合位点(MBS)。Mitchell 启动子 MBS 中的突变使总体启动子活性降低了 50%,突出了增强子区域的重要性。我们表明,EOBII 通过这个 MBS 结合并激活 ODO1 启动子,在这两个调节矮牵牛花香气生物合成的因子之间建立了分子联系。

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