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An Uncanonical CCCH-Tandem Zinc-Finger Protein Represses Secondary Wall Synthesis and Controls Mechanical Strength in Rice

机译:一个不规范的CCCH串联锌指蛋白抑制水稻的次生壁合成并控制机械强度

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摘要

Secondary walls,which represent the bulk of biomass,have a large impact on plant growth and adaptation to environments.Secondary wall synthesis is switched and regulated by a sophisticated signaling transduction network.However,there is limited understanding of these regulatory pathways.Here,we report that ILA1-interacting protein 4 (IIP4) can repress secondary wall synthesis.IIP4 is a phosphorylation sub strate of an Raf-like MAPKKK,but its function is unknown.By generating iip4 mutants and relevant transgenic plants,we found that lesions in IIP4 enhance secondary wall formation.Gene expression and transactivation activity assays revealed that IIP4 negatively regulates the expression of MYB61 and CESAs but does not bind their promoters.IIP4 interacts with NAC29/NAC31,the upstream regulators of secondary wall synthesis,and suppresses the downstream regulatory pathways in plants.Mutagenesis analyses showed that phosphomimic IIP4 proteins translocate from the nucleus to the cytoplasm,which releases interacting NACs and attenuates its repression function.Moreover,we revealed that IIPs are evolutionarily conserved and share unreported CCCH motifs,referred to as uncanonical CCCH-tandem zinc-finger proteins.Collectively,our study provides mechanistic insights into the control of secondary wall synthesis and presents an opportunity for improving relevant agronomic traits in crops.
机译:次生壁代表了生物质的大部分,对植物的生长和对环境的适应有很大的影响。次生壁的合成是通过复杂的信号转导网络进行切换和调控的。然而,对这些调控途径的了解却很有限。报告说,ILA1相互作用蛋白4(IIP4)可以抑制次级壁的合成。IIP4是Raf样MAPKKK的磷酸化底物,但其功能尚不清楚。通过产生iip4突变体和相关的转基因植物,我们发现IIP4的病灶基因表达和反式激活活性测定表明,IIP4负调控MYB61和CESA的表达,但不结合其启动子。IIP4与NAC29 / NAC31相互作用,后者是次级壁合成的上游调节剂,并抑制下游调节途径诱变分析表明,磷酸化IIP4蛋白从细胞核转移到细胞质中。 ch释放相互作用的NAC并减弱其抑制功能。此外,我们揭示了IIP在进化上是保守的,并共享未报告的CCCH基序,称为非经典CCCH串联锌指蛋白。合成,并提供了改善作物相关农艺性状的机会。

著录项

  • 来源
    《分子植物(英文版)》 |2018年第1期|163-174|共12页
  • 作者单位

    State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China;

    University of Chinese Academy of Sciences, Beijing 100049, China;

    State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China;

    State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China;

    University of Chinese Academy of Sciences, Beijing 100049, China;

    State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China;

    State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China;

    University of Chinese Academy of Sciences, Beijing 100049, China;

    State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China;

    State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China;

    State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China;

    State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China;

    University of Chinese Academy of Sciences, Beijing 100049, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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