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Alternative Splicing of Arabidopsis IBR5 Pre-mRNA Generates Two IBR5 Isoforms with Distinct and Overlapping Functions

机译:拟南芥IBR5前mRNA的选择性剪接生成两个具有明显和重叠功能的IBR5亚型。

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摘要

The INDOLE-3-BUTYRIC ACID RESPONSE5 (IBR5) gene encodes a dual specificity phosphatase that regulates plant auxin responses. IBR5 has been predicted to generate two transcripts through alternative splicing, but alternative splicing of IBR5 has not been confirmed experimentally. The previously characterized ibr5-1 null mutant exhibits many auxin related defects such as auxin insensitive primary root growth, defective vascular development, short stature and reduced lateral root development. However, whether all these defects are caused by the lack of phosphatase activity is not clear. Here we describe two new auxin insensitive IBR5 alleles, ibr5-4, a catalytic site mutant, and ibr5-5, a splice site mutant. Characterization of these new mutants indicates that IBR5 is post-transcriptionally regulated to generate two transcripts, AT2G04550.1 and AT2G04550.3, and consequently two IBR5 isoforms, IBR5.1 and IBR5.3. The IBR5.1 isoform exhibits phosphatase catalytic activity that is required for both proper degradation of Aux/IAA proteins and auxin-induced gene expression. These two processes are independently regulated by IBR5.1. Comparison of new mutant alleles with ibr5-1 indicates that all three mutant alleles share many phenotypes. However, each allele also confers distinct defects implicating IBR5 isoform specific functions. Some of these functions are independent of IBR5.1 catalytic activity. Additionally, analysis of these new mutant alleles suggests that IBR5 may link ABP1 and SCFTIR1/AFBs auxin signaling pathways.
机译:INDOLE-3-BUTYRIC ACID RESPONSE5(IBR5)基因编码调节植物生长素反应的双重特异性磷酸酶。预测IBR5可通过选择性剪接产生两个转录本,但是IBR5的选择性剪接尚未通过实验证实。先前表征的ibr5-1 null突变体表现出许多与生长素相关的缺陷,例如生长素不敏感的初生根生长,血管发育不良,身材矮小和侧根发育减少。但是,尚不清楚所有这些缺陷是否是由于缺乏磷酸酶活性引起的。在这里,我们描述了两个新的生长素不敏感的IBR5等位基因,ibr5-4,一个催化位点突变体,和ibr5-5,一个剪接位点突变体。这些新突变体的表征表明,转录后对IBR5进行了调控,以生成两个转录本AT2G04550.1和AT2G04550.3,从而生成了两个IBR5亚型IBR5.1和IBR5.3。 IBR5.1亚型具有磷酸酶催化活性,这是Aux / IAA蛋白正确降解和生长素诱导的基因表达所必需的。这两个过程均由IBR5.1独立调节。新突变等位基因与ibr5-1的比较表明,所有三个突变等位基因均具有许多表型。然而,每个等位基因还赋予了牵涉IBR5亚型特异性功能的独特缺陷。其中一些功能与IBR5.1催化活性无关。此外,对这些新突变等位基因的分析表明,IBR5可能与ABP1和SCF TIR1 / AFBs 生长素信号传导途径有关。

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