IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-37326-x.html
   My bibliography  Save this article

Optimization of rice panicle architecture by specifically suppressing ligand–receptor pairs

Author

Listed:
  • Tao Guo

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture)

  • Zi-Qi Lu

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture
    ShanghaiTech University)

  • Yehui Xiong

    (Tsinghua University)

  • Jun-Xiang Shan

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture)

  • Wang-Wei Ye

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture)

  • Nai-Qian Dong

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture)

  • Yi Kan

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture)

  • Yi-Bing Yang

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture
    University of the Chinese Academy of Sciences)

  • Huai-Yu Zhao

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture
    University of the Chinese Academy of Sciences)

  • Hong-Xiao Yu

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture
    University of the Chinese Academy of Sciences)

  • Shuang-Qin Guo

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture
    University of the Chinese Academy of Sciences)

  • Jie-Jie Lei

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture
    University of the Chinese Academy of Sciences)

  • Ben Liao

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture
    ShanghaiTech University)

  • Jijie Chai

    (Tsinghua University)

  • Hong-Xuan Lin

    (CAS Centre for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences
    Guangdong Laboratory for Lingnan Modern Agriculture
    ShanghaiTech University
    University of the Chinese Academy of Sciences)

Abstract

Rice panicle architecture determines the grain number per panicle and therefore impacts grain yield. The OsER1–OsMKKK10–OsMKK4–OsMPK6 pathway shapes panicle architecture by regulating cytokinin metabolism. However, the specific upstream ligands perceived by the OsER1 receptor are unknown. Here, we report that the EPIDERMAL PATTERNING FACTOR (EPF)/EPF-LIKE (EPFL) small secreted peptide family members OsEPFL6, OsEPFL7, OsEPFL8, and OsEPFL9 synergistically contribute to rice panicle morphogenesis by recognizing the OsER1 receptor and activating the mitogen-activated protein kinase cascade. Notably, OsEPFL6, OsEPFL7, OsEPFL8, and OsEPFL9 negatively regulate spikelet number per panicle, but OsEPFL8 also controls rice spikelet fertility. A osepfl6 osepfl7 osepfl9 triple mutant had significantly enhanced grain yield without affecting spikelet fertility, suggesting that specifically suppressing the OsEPFL6–OsER1, OsEPFL7–OsER1, and OsEPFL9–OsER1 ligand–receptor pairs can optimize rice panicle architecture. These findings provide a framework for fundamental understanding of the role of ligand–receptor signaling in rice panicle development and demonstrate a potential method to overcome the trade-off between spikelet number and fertility.

Suggested Citation

  • Tao Guo & Zi-Qi Lu & Yehui Xiong & Jun-Xiang Shan & Wang-Wei Ye & Nai-Qian Dong & Yi Kan & Yi-Bing Yang & Huai-Yu Zhao & Hong-Xiao Yu & Shuang-Qin Guo & Jie-Jie Lei & Ben Liao & Jijie Chai & Hong-Xuan, 2023. "Optimization of rice panicle architecture by specifically suppressing ligand–receptor pairs," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-37326-x
    DOI: 10.1038/s41467-023-37326-x
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-37326-x
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-37326-x?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Xing Huo & Shuang Wu & Zuofeng Zhu & Fengxia Liu & Yongcai Fu & Hongwei Cai & Xianyou Sun & Ping Gu & Daoxin Xie & Lubin Tan & Chuanqing Sun, 2017. "NOG1 increases grain production in rice," Nature Communications, Nature, vol. 8(1), pages 1-11, December.
    2. Cawas B. Engineer & Majid Ghassemian & Jeffrey C. Anderson & Scott C. Peck & Honghong Hu & Julian I. Schroeder, 2014. "Carbonic anhydrases, EPF2 and a novel protease mediate CO2 control of stomatal development," Nature, Nature, vol. 513(7517), pages 246-250, September.
    3. Xueyong Li & Qian Qian & Zhiming Fu & Yonghong Wang & Guosheng Xiong & Dali Zeng & Xiaoqun Wang & Xinfang Liu & Sheng Teng & Fujimoto Hiroshi & Ming Yuan & Da Luo & Bin Han & Jiayang Li, 2003. "Control of tillering in rice," Nature, Nature, vol. 422(6932), pages 618-621, April.
    4. Shigeo S. Sugano & Tomoo Shimada & Yu Imai & Katsuya Okawa & Atsushi Tamai & Masashi Mori & Ikuko Hara-Nishimura, 2010. "Stomagen positively regulates stomatal density in Arabidopsis," Nature, Nature, vol. 463(7278), pages 241-244, January.
    5. Jin Suk Lee & Marketa Hnilova & Michal Maes & Ya-Chen Lisa Lin & Aarthi Putarjunan & Soon-Ki Han & Julian Avila & Keiko U. Torii, 2015. "Competitive binding of antagonistic peptides fine-tunes stomatal patterning," Nature, Nature, vol. 522(7557), pages 439-443, June.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Sayaka Matsui & Saki Noda & Keiko Kuwata & Mika Nomoto & Yasuomi Tada & Hidefumi Shinohara & Yoshikatsu Matsubayashi, 2024. "Arabidopsis SBT5.2 and SBT1.7 subtilases mediate C-terminal cleavage of flg22 epitope from bacterial flagellin," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    2. Syada Nizer Sultana & Hyun Jo & Jong Tae Song & Kihwan Kim & Jeong-Dong Lee, 2024. "Stomatal Density Variation Within and Among Different Soybean Cultivars Across Various Growth Stages," Agriculture, MDPI, vol. 14(11), pages 1-14, November.
    3. Yuanjie Li & Sheng Wu & Yongyu Huang & Xin Ma & Lubin Tan & Fengxia Liu & Qiming Lv & Zuofeng Zhu & Meixia Hu & Yongcai Fu & Kun Zhang & Ping Gu & Daoxin Xie & Hongying Sun & Chuanqing Sun, 2023. "OsMADS17 simultaneously increases grain number and grain weight in rice," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    4. Chunhao Dong & Lichao Zhang & Qiang Zhang & Yuxin Yang & Danping Li & Zhencheng Xie & Guoqing Cui & Yaoyu Chen & Lifen Wu & Zhan Li & Guoxiang Liu & Xueying Zhang & Cuimei Liu & Jinfang Chu & Guangyao, 2023. "Tiller Number1 encodes an ankyrin repeat protein that controls tillering in bread wheat," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    5. Jinfei Zhang & Yuyi Zhang & Jingguang Chen & Mengfan Xu & Xinyu Guan & Cui Wu & Shunan Zhang & Hongye Qu & Jinfang Chu & Yifeng Xu & Mian Gu & Ying Liu & Guohua Xu, 2024. "Sugar transporter modulates nitrogen-determined tillering and yield formation in rice," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-37326-x. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.