ERECTA genes and their ligands regulate shoot and inflorescence architecture in maize.
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In maize, several yield-related traits are associated with meristem activity, regulated by CLAVATA3/EMBRYO SURROUNDING REGION-related (CLE) peptide signals perceived by CLAVATA(CLV) receptors in the CLAVATA-WUSCHEL (CLV-WUS) pathway. However, additional signaling pathways in maize meristem development remain poorly understood. Here, we identify three receptor-like kinases, ZmERECTA1 (ZmER1), ZmER2 and ZmER1-like (ZmERL), and their ligands, EPIDERMAL PATTERNING FACTOR-like (ZmEPFL), as critical regulators of meristem activity, plant architecture, and ear development. We demonstrate that ZmER receptors act redundantly, with ZmER1 playing a primary role. Zmer1 mutants have compact architecture, enlarged inflorescence meristems (IMs), and increased kernel row numbers (KRNs), while higher-order Zmer mutants display exacerbated phenotypes. We further reveal that ZmER1 specifically binds to five EPFL peptides, which act redundantly in ear development regulation. Furthermore, we find that ZmWUS1 is upregulated in Zmer mutants and mutation in Zmwus1 partially suppress the enlarged IM of Zmer1 mutants. We also generate weak Zmer1 alleles with enhanced yield traits, including reduced leaf angles and increased KRN. These findings offer valuable insights into ER-EPFL signaling in maize meristem development and provide promising genetic targets for breeding high-yield maize varieties through optimized plant and ear architecture.
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Acknowledgements: This work was supported by the National Natural Science Foundation of China (U22A20474 to F.X., U22A20460 to X.H., and 32101741 to F.X.), Natural Science Foundation of Shandong Province (ZR2023JQ012 to F.X.) and the Taishan Scholar Program of Shandong Provincial Government to F.X., and US NSF (Grant IOS-2131631 and IOS-2129189 to D.J.). We thank Prof. Xiaoduo Lu at Qilu Normal University and Prof. Chunyi Zhang at Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, for providing the EMS alleles of Zmer1 and Zmwus1. Thanks to Sen Wang, Haiyan Yu, Xiaomin Zhao and Yuyu Guo from Core Facilities for Life and Environmental Sciences at the SKLMT (State Key Laboratory of Microbial Technology, Shandong University) for the assistance provided in scanning electron microscopy and laser scanning confocal microscopy. We also thank Feng Zhang (Core Facility and Service Platform, School of Life Sciences, Shandong University) for technical support with the SpectraMax® i3x system.
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2041-1723
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Natural Science Foundation of Shandong Province (Shandong Provincial Natural Science Foundation) (ZR2023JQ012)
National Science Foundation (NSF) (IOS-2131631, IOS-2131631)

