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Responses of a Triple Mutant Defective in Three Iron Deficiency-Induced BASIC HELIX-LOOP-HELIX Genes of the Subgroup Ib(2) to Iron Deficiency and Salicylic Acid

机译:Ib(2)亚型的三个铁缺乏诱导的基本HELIX-LOOP-HELIX基因中的三突变体缺陷对铁缺乏和水杨酸的响应

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摘要

Plants are sessile organisms that adapt to external stress by inducing molecular and physiological responses that serve to better cope with the adverse growth condition. Upon low supply of the micronutrient iron, plants actively increase the acquisition of soil iron into the root and its mobilization from internal stores. The subgroup Ib(2) BHLH genes function as regulators in this response, however their concrete functions are not fully understood. Here, we analyzed a triple loss of function mutant of BHLH39, BHLH100 and BHLH101 (3xbhlh mutant). We found that this mutant did not have any iron uptake phenotype if iron was provided. However, under iron deficiency the mutant displayed a more severe leaf chlorosis than the wild type. Microarray-based transcriptome analysis revealed that this mutant phenotype resulted in the mis-regulation of 198 genes, out of which only 15% were associated with iron deficiency regulation itself. A detailed analysis revealed potential targets of the bHLH transcription factors as well as genes reflecting an exaggerated iron deficiency response phenotype. Since the BHLH genes of this subgroup have been brought into the context of the plant hormone salicylic acid, we investigated whether the 3xbhlh mutant might have been affected by this plant signaling molecule. Although a very high number of genes responded to SA, also in a differential manner between mutant and wild type, we did not find any indication for an association of the BHLH gene functions in SA responses upon iron deficiency. In summary, our study indicates that the bHLH subgroup Ib(2) transcription factors do not only act in iron acquisition into roots but in other aspects of the adaptation to iron deficiency in roots and leaves.
机译:植物是固着生物,通过诱导分子和生理反应适应外部胁迫,从而更好地应对不利的生长条件。在微量营养素铁供应不足的情况下,植物会积极增加土壤铁素向根部的吸收及其从内部存储中的迁移。 Ib(2)亚型BHLH基因在此反应中起调节子的作用,但是其具体功能尚不完全清楚。在这里,我们分析了BHLH39,BHLH100和BHLH101(3xbhlh突变体)功能突变体的三重缺失。我们发现,如果提供铁,则该突变体不具有任何铁摄取表型。然而,在铁缺乏的情况下,该突变体比野生型表现出更严重的叶片萎黄病。基于微阵列的转录组分析表明,这种突变表型导致198个基因的调控异常,其中只有15%与铁缺乏调控本身有关。详细的分析揭示了bHLH转录因子的潜在靶标以及反映夸张的铁缺乏反应表型的基因。由于该亚组的BHLH基因已被引入植物激素水杨酸的环境中,因此我们研究了3xbhlh突变体是否已受到该植物信号分子的影响。尽管有大量基因对SA产生反应,但突变型和野生型之间也存在差异,但我们并未发现任何迹象表明BHLH基因功能与铁缺乏时的SA反应有关。总而言之,我们的研究表明,bHLH亚组Ib(2)转录因子不仅在铁的吸收中起作用,而且在根和叶中对铁缺乏适应的其他方面也起作用。

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