Department of Biology, Hong Kong Baptist University, Hong Kong, China.
State Key Laboratory of Environmental and Biological Analysis, Department of Chemistry, Hong Kong Baptist University, Hong Kong, China.
J Integr Plant Biol. 2020 Jul;62(7):967-983. doi: 10.1111/jipb.12867. Epub 2019 Nov 7.
RNA capping and decapping tightly coordinate with transcription, translation, and RNA decay to regulate gene expression. Proteins in the DXO/Rai1 family have been implicated in mRNA decapping and decay, and mammalian DXO was recently found to also function as a decapping enzyme for NAD -capped RNAs (NAD-RNA). The Arabidopsis genome contains a single gene encoding a DXO/Rai1 protein, AtDXO1. Here we show that AtDXO1 possesses both NAD-RNA decapping activity and 5'-3' exonuclease activity but does not hydrolyze the m G cap. The atdxo1 mutation increased the stability of NAD-RNAs and led to pleiotropic phenotypes, including severe growth retardation, pale color, and multiple developmental defects. Transcriptome profiling analysis showed that the atdxo1 mutation resulted in upregulation of defense-related genes but downregulation of photosynthesis-related genes. The autoimmunity phenotype of the mutant could be suppressed by either eds1 or npr1 mutation. However, the various phenotypes associated with the atdxo1 mutant could be complemented by an enzymatically inactive AtDXO1. The atdxo1 mutation apparently enhances post-transcriptional gene silencing by elevating levels of siRNAs. Our study indicates that AtDXO1 regulates gene expression in various biological and physiological processes through its pleiotropic molecular functions in mediating RNA processing and decay.
RNA 的加帽和去帽与转录、翻译和 RNA 降解紧密协调,以调节基因表达。DXO/Rai1 家族的蛋白已被牵连到 mRNA 的去帽和降解中,最近发现哺乳动物的 DXO 也可作为 NAD 加帽 RNA(NAD-RNA)的去帽酶。拟南芥基因组包含一个编码 DXO/Rai1 蛋白的单一基因,AtDXO1。在这里,我们表明 AtDXO1 具有 NAD-RNA 去帽活性和 5'-3' 外切核酸酶活性,但不能水解 mG 帽。atdxo1 突变增加了 NAD-RNAs 的稳定性,并导致多种表型,包括严重的生长迟缓、苍白的颜色和多种发育缺陷。转录组分析表明,atdxo1 突变导致与防御相关的基因上调,但与光合作用相关的基因下调。突变体的自身免疫表型可以通过 eds1 或 npr1 突变来抑制。然而,atdxo1 突变体的各种表型可以通过具有酶失活的 AtDXO1 来互补。atdxo1 突变显然通过提高 siRNA 的水平增强了转录后基因沉默。我们的研究表明,AtDXO1 通过其在介导 RNA 加工和降解中的多种分子功能,在各种生物和生理过程中调节基因表达。