首页> 外文期刊>The Plant Cell >Pathogen-Associated Molecular Pattern-Triggered Immunity Involves Proteolytic Degradation of Core Nonsense-Mediated mRNA Decay Factors During the Early Defense Response([OPEN])
【24h】

Pathogen-Associated Molecular Pattern-Triggered Immunity Involves Proteolytic Degradation of Core Nonsense-Mediated mRNA Decay Factors During the Early Defense Response([OPEN])

机译:病原体相关的分子模式触发的免疫涉及在早期防御响应期间核心废话介导的mRNA衰变因子的蛋白水解降解([打开])

获取原文
获取原文并翻译 | 示例
           

摘要

Nonsense-mediated mRNA decay (NMD), an mRNA quality control process, is thought to function in plant immunity. A subset of fully spliced (FS) transcripts of Arabidopsis (Arabidopsis thaliana) resistance (R) genes are upregulated during bacterial infection. Here, we report that 81.2% and 65.1% of FS natural TIR-NBS-LRR (TNL) and CC-NBS-LRR transcripts, respectively, retain characteristics of NMD regulation, as their transcript levels could be controlled posttranscriptionally. Both bacterial infection and the perception of bacteria by pattern recognition receptors initiated the destruction of core NMD factors UP-FRAMESHIFT1 (UPF1), UPF2, and UPF3 in Arabidopsis within 30 min of inoculation via the independent ubiquitination of UPF1 and UPF3 and their degradation via the 26S proteasome pathway. The induction of UPF1 and UPF3 ubiquitination was delayed in mitogen-activated protein kinase3 (mpk3) and mpk6, but not in salicylic acid-signaling mutants, during the early immune response. Finally, previously uncharacterized TNL-type R transcripts accumulated in upf mutants and conferred disease resistance to infection with a virulent Pseudomonas strain in plants. Our findings demonstrate that NMD is one of the main regulatory processes through which PRRs fine-tune R transcript levels to reduce fitness costs and achieve effective immunity.
机译:无意义介导的mRNA衰减(NMD),mRNA质量控制过程被认为在植物免疫中起作用。在细菌感染期间上调完全剪接(拟南芥)抗性(R)基因的完全剪接(FS)转录物的子集。在这里,我们报告称,81.2%和65.1%的FS天然TIR-NBS-LRR(TN1)和CC-NBS-LRR转录物保留NMD调节的特性,因为它们的转录水平可以被检测到后标记。细菌感染和通过模式识别受体的细菌的感知引发了拟南芥核心NMD因子上的核心NMD因子,UPF2和UPF3,通过独立的UPF1和UPF3和通过它们的降解进行了30分钟内接种的拟南芥。 26s蛋白酶体途径。在早期免疫应答期间,在丝裂剂活化的蛋白激酶3(MPK3)和MPK6中延迟了UPF1和UPF3 ubiquitation的诱导,但不在水杨酸 - 信号突变体中延迟。最后,以前在UPF突变体中积累的不表征TNL型R转录物,并赋予植物中具有毒性假单胞菌菌株的感染抗病性。我们的研究结果表明,NMD是PRRS微调R转录水平的主要监管程序之一,以降低健身成本并实现有效的免疫力。

著录项

  • 来源
    《The Plant Cell》 |2020年第4期|共21页
  • 作者单位

    Dong A Univ Dept Appl Biosci Busan 49315 South Korea;

    Myongji Univ Dept Biosci &

    Bioinformat Yongin 17058 South Korea;

    Dong A Univ Dept Appl Biosci Busan 49315 South Korea;

    Dong A Univ Dept Appl Biosci Busan 49315 South Korea;

    Myongji Univ Dept Biosci &

    Bioinformat Yongin 17058 South Korea;

    Myongji Univ Dept Biosci &

    Bioinformat Yongin 17058 South Korea;

    Dong A Univ Dept Appl Biosci Busan 49315 South Korea;

    Dong A Univ Dept Appl Biosci Busan 49315 South Korea;

    Myongji Univ Dept Biosci &

    Bioinformat Yongin 17058 South Korea;

    Chonnam Natl Univ Dept Biotechnol Yeosu 59626 South Korea;

    Kyung Hee Univ Grad Sch Biotechnol Yongin 17104 South Korea;

    Chung Ang Univ Sch Biol Sci Seoul 06974 South Korea;

    Myongji Univ Dept Biosci &

    Bioinformat Yongin 17058 South Korea;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 植物细胞学;
  • 关键词

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号