Zhong Zhuojun, Yao Minhao, Cao Yingying, Kong Dexin, Wang Baobao, Wang Yanli, Shen Rongxin, Wang Haiyang, Liu Qing
State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangdong Laboratory for Lingnan Modern Agriculture, College of Life Sciences, South China Agricultural University, Guangzhou, Guangdong 510642, China.
Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
J Genet Genomics. 2025 Mar;52(3):356-366. doi: 10.1016/j.jgg.2025.01.014. Epub 2025 Jan 27.
Increasing plant density is an effective strategy for enhancing crop yield per unit land area. A key architectural trait for crops adapting to high planting density is a smaller leaf angle (LA). Previous studies have demonstrated that LG1, a SQUAMOSA BINDING PROTEIN (SBP) transcription factor, plays a critical role in LA establishment. However, the molecular mechanisms underlying the regulation of LG1 on LA formation remain largely unclear. In this study, we conduct comparative RNA-seq analysis of the preligule band (PLB) region of wild type and lg1 mutant leaves. Gene Ontology (GO) term enrichment analysis reveals enrichment of phytohormone pathways and transcription factors, including three auxin transporter genes ZmPIN1a, ZmPIN1b, and ZmPIN1c. Further molecular experiments demonstrate that LG1 can directly bind to the promoter region of these auxin transporter genes and activate their transcription. We also show that double and triple mutants of these ZmPINs genes exhibit varying degrees of auricle size reduction and thus decreased LA. On the contrary, overexpression of ZmPIN1a causes larger auricle and LA. Taken together, our findings establish a functional link between LG1 and auxin transport in regulating PLB formation and provide valuable targets for genetic improvement of LA for breeding high-density tolerant maize cultivars.
增加种植密度是提高单位土地面积作物产量的有效策略。作物适应高种植密度的一个关键株型性状是较小的叶角(LA)。先前的研究表明,LG1作为一种SQUAMOSA结合蛋白(SBP)转录因子,在叶角形成中起关键作用。然而,LG1调控叶角形成的分子机制仍不清楚。在本研究中,我们对野生型和lg1突变体叶片的叶枕前带(PLB)区域进行了比较RNA测序分析。基因本体(GO)术语富集分析显示植物激素途径和转录因子富集,包括三个生长素转运蛋白基因ZmPIN1a、ZmPIN1b和ZmPIN1c。进一步的分子实验表明,LG1可以直接结合这些生长素转运蛋白基因的启动子区域并激活它们的转录。我们还表明,这些ZmPINs基因的双突变体和三突变体表现出不同程度的叶耳大小减小,从而叶角减小。相反,ZmPIN1a的过表达导致叶耳和叶角增大。综上所述,我们的研究结果在调控PLB形成方面建立了LG1与生长素运输之间的功能联系,并为培育耐高密度玉米品种的叶角遗传改良提供了有价值的靶点。