Institute of Plant Biology and Department of Life Science, National Taiwan University, Roosevelt Road, Taipei, 106, Taiwan.
Plant J. 2013 Sep;75(5):781-94. doi: 10.1111/tpj.12238. Epub 2013 Jun 26.
Small RNAs (sRNAs) play important roles in plants under stress conditions. However, limited research has been performed on the sRNAs involved in plant wound responses. In the present study, a novel wounding-induced sRNA, sRNA8105, was identified in sweet potato (Ipomoea batatas cv. Tainung 57) using microarray analysis. It was found that expression of sRNA8105 increased after mechanical wounding. Furthermore, Dicer-like 1 (DCL1) is required for the sRNA8105 precursor (pre-sRNA8105) to generate 22 and 24 nt mature sRNA8105. sRNA8105 targeted the first intron of IbMYB1 (MYB domain protein 1) before RNA splicing, and mediated RNA cleavage and DNA methylation of IbMYB1. The interaction between sRNA8105 and IbMYB1 was confirmed by cleavage site mapping, agro-infiltration analyses, and use of a transgenic sweet potato over-expressing pre-sRNA8105 gene. Induction of IbMYB1-siRNA was observed in the wild-type upon wounding and in transgenic sweet potato over-expressing pre-sRNA8105 gene without wounding, resulting in decreased expression of the whole IbMYB1 gene family, i.e. IbMYB1 and the IbMYB2 genes, and thus directing metabolic flux toward biosynthesis of lignin in the phenylpropanoid pathway. In conclusion, sRNA8105 induced by wounding binds to the first intron of IbMYB1 RNA to methylate IbMYB1, cleave IbMYB1 RNA, and trigger production of secondary siRNAs, further repressing the expression of the IbMYB1 family genes and regulating the phenylpropanoid pathway.
小 RNA(sRNAs)在植物应激条件下发挥着重要作用。然而,对于参与植物创伤响应的 sRNAs 的研究还很有限。本研究利用微阵列分析在甘薯(Ipomoea batatas cv. Tainung 57)中鉴定出一种新的创伤诱导 sRNA,sRNA8105。研究发现,机械创伤后 sRNA8105 的表达增加。此外,Dicer-like 1(DCL1)对于 sRNA8105 前体(pre-sRNA8105)生成 22 和 24 nt 成熟 sRNA8105 是必需的。sRNA8105 在 RNA 剪接之前靶向 IbMYB1(MYB 结构域蛋白 1)的第一个内含子,并介导 IbMYB1 的 RNA 切割和 DNA 甲基化。通过切割位点作图、农杆菌浸润分析和过表达 pre-sRNA8105 基因的转基因甘薯证实了 sRNA8105 与 IbMYB1 的相互作用。在野生型中观察到 IbMYB1-siRNA 的诱导,在过表达 pre-sRNA8105 基因的转基因甘薯中没有创伤,导致整个 IbMYB1 基因家族(即 IbMYB1 和 IbMYB2 基因)的表达降低,从而指导木质素生物合成代谢流在苯丙素途径中。总之,创伤诱导的 sRNA8105 结合到 IbMYB1 RNA 的第一个内含子上,使 IbMYB1 甲基化,切割 IbMYB1 RNA,并引发次生 siRNA 的产生,进一步抑制 IbMYB1 家族基因的表达,调节苯丙素途径。