首页> 美国卫生研究院文献>Molecular Biology and Evolution >Synergistic Binding of bHLH Transcription Factors to the Promoter of the Maize NADP-ME Gene Used in C4 Photosynthesis Is Based on an Ancient Code Found in the Ancestral C3 State
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Synergistic Binding of bHLH Transcription Factors to the Promoter of the Maize NADP-ME Gene Used in C4 Photosynthesis Is Based on an Ancient Code Found in the Ancestral C3 State

机译:bHLH转录因子与玉米NADP-ME基因启动子(用于C4光合作用)的启动子的协同结合是基于在祖先C3状态中发现的古老密码

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摘要

C4 photosynthesis has evolved repeatedly from the ancestral C3 state to generate a carbon concentrating mechanism that increases photosynthetic efficiency. This specialized form of photosynthesis is particularly common in the PACMAD clade of grasses, and is used by many of the world’s most productive crops. The C4 cycle is accomplished through cell-type-specific accumulation of enzymes but cis-elements and transcription factors controlling C4 photosynthesis remain largely unknown. Using the NADP-Malic Enzyme (NADP-ME) gene as a model we tested whether mechanisms impacting on transcription in C4 plants evolved from ancestral components found in C3 species. Two basic Helix-Loop-Helix (bHLH) transcription factors, ZmbHLH128 and ZmbHLH129, were shown to bind the C4NADP-ME promoter from maize. These proteins form heterodimers and ZmbHLH129 impairs trans-activation by ZmbHLH128. Electrophoretic mobility shift assays indicate that a pair of cis-elements separated by a seven base pair spacer synergistically bind either ZmbHLH128 or ZmbHLH129. This pair of cis-elements is found in both C3 and C4 Panicoid grass species of the PACMAD clade. Our analysis is consistent with this cis-element pair originating from a single motif present in the ancestral C3 state. We conclude that C4 photosynthesis has co-opted an ancient C3 regulatory code built on G-box recognition by bHLH to regulate the NADP-ME gene. More broadly, our findings also contribute to the understanding of gene regulatory networks controlling C4 photosynthesis.
机译:C4的光合作用已从祖先的C3状态反复演化,以产生提高光合作用效率的碳浓缩机制。这种特殊的光合作用形式在PACMAD草丛中尤为常见,并且被世界上许多生产力最高的农作物所采用。 C4循环是通过酶的细胞类型特异性积累来完成的,但控制C4光合作用的顺式元件和转录因子仍然未知。我们使用NADP-苹果酸酶(NADP-ME)基因作为模型,测试了影响C4植物转录的机制是否从C3物种的祖先成分进化而来。两种基本的Helix-Loop-Helix(bHLH)转录因子ZmbHLH128和ZmbHLH129与玉米的C4NADP-ME启动子结合。这些蛋白质形成异二聚体,ZmbHLH129损害ZmbHLH128的反式激活。电泳迁移率变动分析表明,一对被七个碱基对间隔子隔开的顺式元件可协同结合ZmbHLH128或ZmbHLH129。在PACMAD进化枝的C3和C4 Panicoid草种中都发现了这对顺式元素。我们的分析与这种源自祖先C3状态的单个基序的顺式元件对一致。我们得出的结论是,C4光合作用已采用了一种古老的C3调控密码,该密码基于bHLH的G-box识别来调节NADP-ME基因。更广泛地说,我们的发现也有助于理解控制C4光合作用的基因调控网络。

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