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Cloning and characterization of the Iron-Regulated Transporter (IRT) genes and their transcription factors in Populus.

机译:毛白杨铁调控转运蛋白(IRT)基因及其转录因子的克隆与鉴定。

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摘要

Iron deficiency causes chlorosis in many plant species, resulting in yield loss and poor quality. Many tree species including poplar are susceptible to iron deficiency. Trees suffering from iron deficiency often show interveinal chlorotic leaves and in severe cases, branches or an entire tree may die.;In this study, two trees of Populus tremula L.`Erecta' growing near each other but with contrasting leaf color phenotypes were used to study the causes of chlorosis and the mechanisms of tolerance or susceptibility to iron chlorosis in poplar. A leaf analysis revealed that the iron deficiency tolerant tree (PtG) had a higher level of dry matter content, chlorophyll (a+b), Chl a/b ratio, Zn and Fe content than the iron chlorosis susceptible tree (PtY). A hydroponic culture confirmed the differences in aforementioned physiological parameters between PtG and PtY responding to iron deficiency.;Two iron-regulated transporter genes (PtIRT1 and PtIRT3), the native promoter of the PtIRT1 gene (PtIRT1-pro), and two basic helix-loop-helix (bHLH) transcription factors (PtFIT and PtIRO) were cloned and characterized for their responses to iron deficiency in PtG and PtY. Deduced amino acid analysis revealed that PtIRT1, PtIRT3, PtFIT, and PtIRO in PtG were identical to those in PtY. Phylogenetic and putative domain analyses showed that PtIRT1, PtFIT, and PtIRO may function in iron homeostasis, while PtIRT3 may play a role in zinc transport in poplar. The expression of PtIRT1 and PtFIT are root-specific and up-regulated by iron deficiency. The expression of a GUS gene derived by PtIRT1-pro in tobacco was also up-regulated by iron deficiency, but was not root-specific. The expression of PtIRT3 is ubiquitous and up-regulated by iron deficiency, but significantly down-regulated by zinc deficiency. A high correlation in the expression between PtFIT and PtIRT1 was observed in PtG, but not in PtY. Transgenic poplars overexpressing PtIRT1 or PtIRT3 did not have enhanced Fe accumulation; however, an enhanced tolerance to iron deficiency was found in transgenic plants overexpressing PtFIT. The results suggested that the transcription factor PtFIT may be involved in iron deficiency response through regulation of PtIRT1 and PtFIT itself may be regulated by other factors in poplar.
机译:缺铁会导致许多植物发生绿化,导致产量下降和质量下降。许多树种,包括杨树,都容易缺铁。缺铁的树木通常显示出叶绿素的叶,在严重的情况下,树枝或整棵树可能会死亡。在这项研究中,使用了两棵彼此靠近生长但叶色表型相反的杨树。研究杨树萎黄病的成因及对黄萎病的耐受性或敏感性机制。叶片分析表明,耐缺铁树(PtG)的干物质含量,叶绿素(a + b),Chl a / b比,Zn和Fe含量均高于易受铁黄萎病的树(PtY)。水培培养证实了PtG和PtY对缺铁反应的上述生理参数存在差异。;两个铁调节转运蛋白基因(PtIRT1和PtIRT3),PtIRT1基因的天然启动子(PtIRT1-pro)和两个基本螺旋-克隆了环螺旋(bHLH)转录因子(PtFIT和PtIRO),并对它们对PtG和PtY中铁缺乏的反应进行了表征。推导的氨基酸分析表明,PtG中的PtIRT1,PtIRT3,PtFIT和PtIRO与PtY中的相同。系统发育和推定域分析表明,PtIRT1,PtFIT和PtIRO可能在铁稳态中起作用,而PtIRT3可能在杨树的锌转运中起作用。 PtIRT1和PtFIT的表达是根特异性的,并受铁缺乏上调。缺铁也上调了PtIRT1-pro衍生的GUS基因在烟草中的表达,但不是根特异性的。 PtIRT3的表达普遍存在,并受铁缺乏上调,但受锌缺乏显着下调。在PtG中观察到PtFIT和PtIRT1之间的表达高度相关,而在PtY中则没有。过表达PtIRT1或PtIRT3的转基因杨树没有增强的Fe积累。然而,在过表达PtFIT的转基因植物中发现对铁缺乏的耐受性增强。结果表明,转录因子PtFIT可能通过调节PtIRT1参与铁缺乏反应,而PtFIT本身也可能受杨树其他因子的调节。

著录项

  • 作者

    Huang, Danqiong.;

  • 作者单位

    North Dakota State University.;

  • 授予单位 North Dakota State University.;
  • 学科 Plant sciences.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 148 p.
  • 总页数 148
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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