State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China, Sichuan Agricultural University at Wenjiang, 211 Huimin Road, Chengdu, Sichuan, 611130, China.
College of Environmental Science & Engineering, China West Normal University, 1 Shida Road, Nanchong, Sichuan, 637002, China.
Plant J. 2022 Apr;110(1):166-178. doi: 10.1111/tpj.15663. Epub 2022 Feb 8.
Many rice microRNAs have been identified as fine-tuning factors in the regulation of agronomic traits and immunity. Among them, Osa-miR535 targets SQUAMOSA promoter binding protein-like 14 (OsSPL14) to positively regulate tillers but negatively regulate yield and immunity. Here, we uncovered that Osa-miR535 targets another SPL gene, OsSPL4, to suppress rice immunity against Magnaporthe oryzae. Overexpression of Osa-miR535 significantly decreased the accumulation of the fusion protein SPL4 -YFP that contains the target site of Osa-miR535 in OsSPL4. Consistently, Osa-miR535 mediated the cleavage of OsSPL4 mRNA between the 10th and 11th base pair of the predicted binding site at the 3' untranslated region. Transgenic rice lines overexpressing OsSPL4 (OXSPL4) displayed enhanced blast disease resistance accompanied by enhanced immune responses, including increased expression of defense-relative genes and up-accumulated H O . By contrast, the knockout mutant osspl4 exhibited susceptibility. Moreover, OsSPL4 binds to the promoter of GH3.2, an indole-3-acetic acid-amido synthetase, and promotes its expression. Together, these data indicate that Os-miR535 targets OsSPL4 and OsSPL4-GH3.2, which may parallel the OsSPL14-WRKY45 module in rice blast disease resistance.
许多水稻 microRNA 被鉴定为调节农艺性状和免疫的微调因子。其中,Osa-miR535 靶向 SQUAMOSA 启动子结合蛋白样 14(OsSPL14),正向调节分蘖,但负向调节产量和免疫。在这里,我们发现 Osa-miR535 靶向另一个 SPL 基因 OsSPL4,以抑制水稻对稻瘟病菌的免疫。过表达 Osa-miR535 显著降低了包含 Osa-miR535 靶位点的融合蛋白 SPL4-YFP 的积累。一致地,Osa-miR535 在 OsSPL4 的 3'非翻译区预测结合位点的第 10 和第 11 个碱基对之间介导 OsSPL4 mRNA 的切割。过表达 OsSPL4(OXSPL4)的转基因水稻系表现出增强的稻瘟病抗性,伴随着增强的免疫反应,包括防御相关基因的表达增加和 H O 的积累增加。相比之下,敲除突变体 osspl4 表现出易感性。此外,OsSPL4 结合到 GH3.2 的启动子上,GH3.2 是一种吲哚-3-乙酸酰胺合成酶,并促进其表达。总之,这些数据表明 Os-miR535 靶向 OsSPL4 和 OsSPL4-GH3.2,这可能与水稻稻瘟病抗性中的 OsSPL14-WRKY45 模块平行。