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The Ethylene Responsive Factor Required for Nodulation 1 (ERN1) Transcription Factor Is Required for Infection-Thread Formation in Lotus japonicus

机译:莲花中感染线形成需要结瘤1(ERN1)转录因子所需的乙烯响应因子。

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Several hundred genes are transcriptionally regulated during infection-thread formation and development of nitrogen-fixing root nodules. We have characterized a set of Lotus japonicus mutants impaired in root-nodule formation and found that the causative gene, Ern1, encodes a protein with a characteristic APETALA2/Ethylene Responsive Factor (AP2/ERF) transcription-factor domain. Phenotypic characterization of four ern1 alleles shows that infection pockets are formed but root-hair infection threads are absent. Formation of root-nodule primordia is delayed and no normal transcellular infection threads are found in the infected nodules. Corroborating the role of ERN1 (ERF Required for Nodulation1) in nodule organogenesis, spontaneous nodulation induced by an autoactive CCaMK and cytokinin–induced nodule primordia were not observed in ern1 mutants. Expression of Ern1 is induced in the susceptible zone by Nod factor treatment or rhizobial inoculation. At the cellular level, the pErn1:GUS reporter is highly expressed in root epidermal cells of the susceptible zone and in the cortical cells that form nodule primordia. The genetic regulation of this cellular expression pattern was further investigated in symbiotic mutants. Nod factor induction of Ern1 in epidermal cells was found to depend on Nfr1, Cyclops, and Nsp2 but was independent of Nin and Nf-ya1. These results suggest that ERN1 functions as a transcriptional regulator involved in the formation of infection threads and development of nodule primordia and may coordinate these two processes.
机译:在感染线形成和固氮根瘤的发育过程中,数百个基因受到转录调控。我们已经定性了一组在根瘤形成中受损的Lotus japonicus突变体,并发现致病基因Ern1编码具有特征性APETALA2 /乙烯响应因子(AP2 / ERF)转录因子结构域的蛋白质。四个ern1等位基因的表型表征表明,形成了感染袋,但没有根毛感染线。根瘤原基的形成被延迟,在被感染的结节中未发现正常的跨细胞感染线。证实ERN1(结节1所需的ERF)在结节器官发生中的作用,在ern1突变体中未观察到由自发CCaMK和细胞分裂素诱导的结节原基诱导的自发结节。通过Nod因子处理或根瘤菌接种在敏感区域诱导Ern1的表达。在细胞水平上,pErn1:GUS报告基因在易感区的根表皮细胞和形成结节原基的皮质细胞中高度表达。在共生突变体中进一步研究了这种细胞表达模式的遗传调控。发现表皮细胞中Ern1的Nod因子诱导依赖于Nfr1,Cyclops和Nsp2,但独立于Nin和Nf-ya1。这些结果表明,ERN1充当转录调节因子,参与感染线的形成和结节原基的形成,并可能协调这两个过程。

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