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首页> 外文期刊>Plant physiology >Novel Stress-Inducible Antisense RNAs of Protein-Coding Loci Are Synthesized by RNA-Dependent RNA Polymerase
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Novel Stress-Inducible Antisense RNAs of Protein-Coding Loci Are Synthesized by RNA-Dependent RNA Polymerase

机译:通过RNA依赖性RNA聚合酶合成蛋白质编码基因座的新型应激诱导的反义RNA

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摘要

Our previous study identified approximately 6,000 abiotic stress-responsive noncoding transcripts existing on the antisense strand of protein-coding genes and implied that a type of antisense RNA was synthesized from a sense RNA template by RNA-dependent RNA polymerase (RDR). Expression analyses revealed that the expression of novel abiotic stress-induced antisense RNA on 1,136 gene loci was reduced in the rdr1/2/6 mutants. RNase protection indicated that the RD29A antisense RNA and other RDR1/2/6-dependent antisense RNAs are involved in the formation of dsRNA. The accumulation of stress-inducible antisense RNA was decreased and increased in dcp5 and xrn4, respectively, but not changed in dcl2/3/4, nrpd1a and nrpd1b. RNA-seq analyses revealed that the majority of the RDR1/2/6-dependent antisense RNA loci did not overlap with RDR1/2/6-dependent 20-30 nt RNA loci. Additionally, rdr1/2/6 mutants decreased the degradation rate of the sense RNA and exhibited arrested root growth during the recovery stage following a drought stress, whereas dcl2/3/4 mutants did not. Collectively, these results indicate that RDRs have stress-inducible antisense RNA synthesis activity and a novel biological function that is different from the known endogenous small RNA pathways from protein-coding genes. These data reveal a novel mechanism of RNA regulation during abiotic stress response that involves complex RNA degradation pathways.
机译:我们以前的研究确定了大约6,000名存在于蛋白质编码基因的非反义链中的非生物应激响应性非编码转录物,并暗示通过RNA依赖性RNA聚合酶(RDR)从感测RNA模板中合成一种类型的反义RNA。表达分析表明,在RDR1 / 2/6突变体中降低了1,136基因座上的新型非生物胁迫诱导的反义RNA的表达。 RNase保护表明,RD29A反义RNA和其他RDR1 / 2/6依赖性的反义RNA参与DSRNA的形成。分别在DCP5和XRN4中累积应激诱导的反义RNA的积累,但在DCL2 / 3/4,NRPD1A和NRPD1B中不变。 RNA-SEQ分析显示,大多数RDR1 / 2/6依赖性反义RNA基因座没有与RDR1 / 2/6依赖性20-30nt RNA基因座重叠。另外,RDR1 / 2/6突变体降低了感测RNA的降解率,并且在干旱胁迫后在恢复期间表现出被捕的根生长,而DCL2 / 3/4突变体没有。总的来说,这些结果表明RDR具有应激诱导的反义RNA合成活性和新的生物学功能,其与来自蛋白质编码基因的已知内源性小RNA途径不同。这些数据揭示了涉及复杂的RNA降解途径的非生物应激响应期间RNA调节的新机制。

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  • 来源
    《Plant physiology》 |2017年第1期|共16页
  • 作者单位

    RIKEN Ctr Sustainable Resource Sci Plant Genom Network Res Team Tsurumi Ku 1-7-22 Suehiro Cho Yokohama Kanagawa 2300045 Japan;

    Kyoto Univ Grad Sch Med Kyoto 6068501 Japan;

    RIKEN Ctr Sustainable Resource Sci Plant Genom Network Res Team Tsurumi Ku 1-7-22 Suehiro Cho Yokohama Kanagawa 2300045 Japan;

    Natl Inst Basic Biol NIBB Core Res Facil Okazaki Aichi 4448585 Japan;

    RIKEN Ctr Sustainable Resource Sci Plant Genom Network Res Team Tsurumi Ku 1-7-22 Suehiro Cho Yokohama Kanagawa 2300045 Japan;

    RIKEN Ctr Sustainable Resource Sci Plant Genom Network Res Team Tsurumi Ku 1-7-22 Suehiro Cho Yokohama Kanagawa 2300045 Japan;

    RIKEN Ctr Sustainable Resource Sci Plant Genom Network Res Team Tsurumi Ku 1-7-22 Suehiro Cho Yokohama Kanagawa 2300045 Japan;

    RIKEN Adv Ctr Comp &

    Commun Computat Engn Applicat Unit 2-1 Hirosawa Wako Saitama 3510198 Japan;

    Natl Inst Basic Biol NIBB Core Res Facil Okazaki Aichi 4448585 Japan;

    RIKEN Ctr Sustainable Resource Sci Gene Discovery Res Grp Tsurumi Ku 1-7-22 Suehiro Cho Yokohama Kanagawa 2300045 Japan;

    RIKEN Ctr Sustainable Resource Sci Plant Genom Network Res Team Tsurumi Ku 1-7-22 Suehiro Cho Yokohama Kanagawa 2300045 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 植物生理学;
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