Matsui Akihiro, Iida Kei, Tanaka Maho, Yamaguchi Katsushi, Mizuhashi Kayoko, Kim Jong-Myong, Takahashi Satoshi, Kobayashi Norio, Shigenobu Shuji, Shinozaki Kazuo, Seki Motoaki
Plant Genomic Network Research Team, RIKEN Center for Sustainable Resource Science, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan.
Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.
Plant Physiol. 2017 Sep;175(1):457-472. doi: 10.1104/pp.17.00787. Epub 2017 Jul 14.
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 (). Expression analyses revealed that the expression of novel abiotic stress-induced antisense RNA on 1,136 gene loci was reduced in the mutants. RNase protection indicated that the 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 and , respectively, but not changed in , and 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, mutants decreased the degradation rate of the sense RNA and exhibited arrested root growth during the recovery stage following a drought stress, whereas 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.
我们之前的研究在蛋白质编码基因的反义链上鉴定出了大约6000个非生物胁迫响应非编码转录本,并暗示一种反义RNA是由()以正义RNA模板合成的。表达分析表明,在1136个基因位点上,新的非生物胁迫诱导反义RNA在()突变体中的表达降低。核糖核酸酶保护实验表明,()反义RNA和其他依赖RDR1/2/6的反义RNA参与双链RNA的形成。胁迫诱导反义RNA的积累在()中分别减少和增加,但在()中没有变化。RNA测序分析表明,大多数依赖RDR1/2/6的反义RNA位点与依赖RDR1/2/6的20 - 30 nt RNA位点不重叠。此外,()突变体降低了正义RNA的降解速率,并在干旱胁迫后的恢复阶段表现出根系生长停滞,而()突变体则没有。总体而言,这些结果表明RDR具有胁迫诱导的反义RNA合成活性和一种不同于已知蛋白质编码基因内源性小RNA途径的新生物学功能。这些数据揭示了非生物胁迫响应过程中涉及复杂RNA降解途径的一种新的RNA调控机制。