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首页> 外文期刊>The Plant Cell >EFD Is an ERF Transcription Factor Involved in the Control of Nodule Number and Differentiation in Medicago truncatula
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EFD Is an ERF Transcription Factor Involved in the Control of Nodule Number and Differentiation in Medicago truncatula

机译:EFD是ERF转录因子,参与了run藜苜蓿根瘤数量和分化的控制。

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Mechanisms regulating legume root nodule development are still poorly understood, and very few regulatory genes have been cloned and characterized. Here, we describe EFD (for ethylene response factor required for nodule differentiation), a gene that is upregulated during nodulation in Medicago truncatula. The EFD transcription factor belongs to the ethylene response factor (ERF) group V, which contains ERN1, 2, and 3, three ERFs involved in Nod factor signaling. The role of EFD in the regulation of nodulation was examined through the characterization of a null deletion mutant (efd-1), RNA interference, and overexpression studies. These studies revealed that EFD is a negative regulator of root nodulation and infection by Rhizobium and that EFD is required for the formation of functional nitrogen-fixing nodules. EFD appears to be involved in the plant and bacteroid differentiation processes taking place beneath the nodule meristem. We also showed that EFD activated Mt RR4, a cytokinin primary response gene that encodes a type-A response regulator. We propose that EFD induction of Mt RR4 leads to the inhibition of cytokinin signaling, with two consequences: the suppression of new nodule initiation and the activation of differentiation as cells leave the nodule meristem. Our work thus reveals a key regulator linking early and late stages of nodulation and suggests that the regulation of the cytokinin pathway is important both for nodule initiation and development.
机译:调节豆类根瘤发育的机制仍知之甚少,而且很少有调节基因被克隆和鉴定。在这里,我们描述了EFD(针对结节分化所需的乙烯反应因子),该基因在Medi藜苜蓿的结瘤过程中被上调。 EFD转录因子属于乙烯反应因子(ERF)组V,该组包含ERN1、2和3,这三个与Nod因子信号传导有关的ERF。通过表征缺失缺失突变体(efd-1),RNA干扰和过表达研究,研究了EFD在结节调节中的作用。这些研究表明,EFD是根瘤和根瘤菌感染的负调节剂,而EFD是形成功能性固氮根瘤所必需的。 EFD似乎与根瘤分生组织下发生的植物和类细菌分化过程有关。我们还表明,EFD激活了Mt RR4,一种编码A型应答调节因子的细胞分裂素主要应答基因。我们提出,EFD诱导Mt RR4导致细胞分裂素信号转导的抑制,具有两个后果:抑制新的结节起始和分化激活,因为细胞离开了结节分生组织。因此,我们的工作揭示了结瘤早期和晚期阶段之间的关键调节剂,并表明细胞分裂素途径的调节对于结节的起始和发育均很重要。

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