State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, School of Life Sciences, Hubei University, Wuhan, 430062, China.
Huazhong Agricultural University, Wuhan, 430070, China.
Plant J. 2022 Aug;111(4):1167-1182. doi: 10.1111/tpj.15884. Epub 2022 Jul 18.
As a multigenic trait, rice tillering can optimize plant architecture for the maximum agronomic yield. SQUAMOSA PROMOTER BINDING PROTEIN-LIKE14 (OsSPL14) has been demonstrated to be necessary and sufficient to inhibit rice branching, but the underlying mechanism remains largely unclear. Here, we demonstrated that OsSPL14, which is cleaved by miR529 and miR156, inhibits tillering by fine-tuning auxin transport in rice. RNA interference of OsSPL14 or miR529 and miR156 overexpression significantly increased the tiller number, whereas OsSPL14 overexpression decreased the tiller number. Histological analysis revealed that the OsSPL14-overexpressing line had normal initiation of axillary buds but inhibited outgrowth of tillers. Moreover, OsSPL14 was found to be responsive to indole-acetic acid and 1-naphthylphthalamic acid, and RNA interference of OsSPL14 reduced polar auxin transport and increased 1-naphthylphthalamic acid sensitivity of rice plants. Further analysis revealed that OsSPL14 directly binds to the promoter of PIN-FORMED 1b (OsPIN1b) and PIN-LIKE6b (PILS6b) to regulate their expression positively. OsPIN1b and PILS6b were highly expressed in axillary buds and proved involved in bud outgrowth. Loss of function of OsPIN1b or PILS6b increased the tiller number of rice. Taken together, our findings suggested that OsSPL14 could control axillary bud outgrowth and tiller number by activating the expression of OsPIN1b and PILS6b to fine-tune auxin transport in rice.
作为一个多基因性状,水稻分蘖可以优化植物结构,以实现最大的农业产量。已经证明,SQUAMOSA PROMOTER BINDING PROTEIN-LIKE14(OsSPL14)对于抑制水稻分枝是必要且充分的,但潜在的机制在很大程度上仍不清楚。在这里,我们证明了 OsSPL14 可以被 miR529 和 miR156 切割,通过微调生长素运输来抑制水稻分蘖。OsSPL14 的 RNA 干扰或 miR529 和 miR156 的过表达显著增加了分蘖数,而 OsSPL14 的过表达则减少了分蘖数。组织学分析表明,OsSPL14 过表达系具有正常腋芽的起始,但抑制了分蘖的生长。此外,发现 OsSPL14 对吲哚-3-乙酸和 1-萘基邻氨甲酰苯甲酸(1-Naphthylphthalamic acid,NPA)有反应,并且 OsSPL14 的 RNA 干扰降低了极性生长素的运输,并增加了水稻对 1-萘基邻氨甲酰苯甲酸的敏感性。进一步的分析表明,OsSPL14 直接结合到 PIN-FORMED 1b(OsPIN1b)和 PIN-LIKE6b(PILS6b)的启动子上,以正向调节它们的表达。OsPIN1b 和 PILS6b 在腋芽中高度表达,并被证明参与芽的生长。OsPIN1b 或 PILS6b 的功能丧失增加了水稻的分蘖数。综上所述,我们的研究结果表明,OsSPL14 可以通过激活 OsPIN1b 和 PILS6b 的表达来控制侧芽的生长和分蘖数,从而微调生长素在水稻中的运输。