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AUXIN RESPONSE FACTOR1 and AUXIN RESPONSE FACTOR2 regulate senescence and floral organ abscission in Arabidopsis thaliana.

机译:AUXIN响应因子1和AUXIN响应因子2调节拟南芥的衰老和花器官的脱落。

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摘要

In plants, both endogenous mechanisms and environmental signals regulate developmental transitions such as seed germination, induction of flowering, leaf senescence and shedding of senescent organs. Auxin response factors (ARFs) are transcription factors that mediate responses to the plant hormone auxin. We have examined Arabidopsis lines carrying T-DNA insertions in AUXIN RESPONSE FACTOR1 (ARF1) and ARF2 genes. We found that ARF2 promotes transitions between multiple stages of Arabidopsis development. arf2 mutant plants exhibited delays in several processes related to plant aging, including initiation of flowering, rosette leaf senescence, floral organ abscission and silique ripening. ARF2 expression was induced in senescing leaves. ARF2 regulated leaf senescence and floral organ abscission independently of the ethylene and cytokinin response pathways. arf1 mutations enhanced many arf2 phenotypes, indicating that ARF1 acts in a partially redundant manner with ARF2. However, unlike arf2 mutations, an arf1 mutation increased transcription of Aux/IAA genes in Arabidopsis flowers, supporting previous biochemical studies that indicated that ARF1 is a transcriptional repressor. Two other ARF genes, NPH4/ARF7 and ARF19, were also induced by senescence, and mutations in these genes enhanced arf2 phenotypes. NPH4/ARF7 and ARF19 function as transcriptional activators, suggesting that auxin may control senescence in part by activating gene expression.
机译:在植物中,内源性机制和环境信号均调节发育过渡,例如种子发芽,诱导开花,叶片衰老和衰老器官脱落。生长素应答因子(ARF)是介导对植物激素生长素的应答的转录因子。我们检查了在AUXIN RESPONSE FACTOR1(ARF1)和ARF2基因中携带T-DNA插入的拟南芥系。我们发现ARF2促进拟南芥发育的多个阶段之间的过渡。 arf2突变植物在一些与植物衰老相关的过程中表现出延迟,包括开花的开始,莲座叶的衰老,花器官的脱落和角果成熟。在衰老的叶片中诱导了ARF2表达。 ARF2调节叶片衰老和花器官的脱落,而与乙烯和细胞分裂素应答途径无关。 arf1突变增强了许多arf2表型,表明ARF1与ARF2以部分冗余的方式起作用。但是,与arf2突变不同,arf1突变增加了拟南芥花中Aux / IAA基因的转录,从而支持先前的生化研究表明ARF1是转录阻遏物。衰老也诱导了另外两个ARF基因NPH4 / ARF7和ARF19,这些基因中的突变增强了arf2表型。 NPH4 / ARF7和ARF19充当转录激活因子,提示生长素可能通过激活基因表达来部分控制衰老。

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