Rice Science
  • 首页
  • 期刊介绍
  • 编委会
  • 学术伦理
  • 投稿指南
  • 期刊订阅
  • 联系我们
  • English

Rice Science ›› 2025, Vol. 32 ›› Issue (5): 589-593.DOI: 10.1016/j.rsci.2025.03.007

• • 上一篇    下一篇

  • 收稿日期:2025-01-06 接受日期:2025-03-18 出版日期:2025-09-28 发布日期:2025-10-11

RichHTML

PDF

补充材料

1

可视化

0
  • 1. Supplemental Data.pdf(3389KB)

摘要/Abstract

引用本文

. [J]. Rice Science, 2025, 32(5): 589-593.

使用本文

推荐

导出引用管理器 EndNote|Ris|BibTeX

链接本文: http://www.ricesci.org/CN/10.1016/j.rsci.2025.03.007

               http://www.ricesci.org/CN/Y2025/V32/I5/589

图/表 2

Fig. 1. Iron deficiency is primary cause of lesion phenotype in osacl-a2 mutants. A and B, Lesion mimic phenotype in individual plant (A) and leaf (B) of wild type (WT) and osacl-a2 at the tillering stage (at 60 d after seed sowing) in the paddy field. Scale bars, 10 cm. C and D, ATP-citrate lyase (ACL) activity (C) and citric acid content (D) in leaves of WT and osacl-a2 at the heading stage. E, Iron (Fe) content in leaves of WT and osacl-a2 at the tillering stage in natural environment. F, Phenotype of WT and osacl-a2 leaves treated with the indicated exogenous Fe3+ concentrations at two weeks after germination. S-Fe3+, Starvation (0 μmol/L Fe3+); N-Fe3+, Normal (50 μmol/L Fe3+); E-Fe3+, Excess (500 μmol/L Fe3+). Scale bar, 2 cm. G, Images of the magnified part of rice stems in WT and osacl-a2 treated with the indicated exogenous Fe3+ concentrations at two weeks after germination. Scale bars, 40 μm. H-J, Citric acid content (H), ACL activity (I), and Fe content (J) in leaves of WT and osacl-a2 treated with the indicated exogenous Fe3+ concentrations at two weeks after germination. K-N, Relative expression levels of genes (K, OsFER2; L, OsIRO2; M, OsYSL2; and N, OsFRDL1) related to Fe3+ absorption and transport in WT and osacl-a2 treated with the indicated exogenous Fe3+ concentrations at two weeks after germination. Ubiquitin (LOC_Os06g46770) was used as the internal control. Data in C-E and H-J are mean ± SE (n = 3). ** indicates significant differences at the 0.01 level by Student’s t-test.In K-N, different lowercase letters above bars indicate significant differences at P < 0.05 by Tukey’s multiple comparisons test.

Fig. 1. Iron deficiency is primary cause of lesion phenotype in osacl-a2 mutants. A and B, Lesion mimic phenotype in individual plant (A) and leaf (B) of wild type (WT) and osacl-a2 at the tillering stage (at 60 d after seed sowing) in the paddy field. Scale bars, 10 cm. C and D, ATP-citrate lyase (ACL) activity (C) and citric acid content (D) in leaves of WT and osacl-a2 at the heading stage. E, Iron (Fe) content in leaves of WT and osacl-a2 at the tillering stage in natural environment. F, Phenotype of WT and osacl-a2 leaves treated with the indicated exogenous Fe3+ concentrations at two weeks after germination. S-Fe3+, Starvation (0 μmol/L Fe3+); N-Fe3+, Normal (50 μmol/L Fe3+); E-Fe3+, Excess (500 μmol/L Fe3+). Scale bar, 2 cm. G, Images of the magnified part of rice stems in WT and osacl-a2 treated with the indicated exogenous Fe3+ concentrations at two weeks after germination. Scale bars, 40 μm. H-J, Citric acid content (H), ACL activity (I), and Fe content (J) in leaves of WT and osacl-a2 treated with the indicated exogenous Fe3+ concentrations at two weeks after germination. K-N, Relative expression levels of genes (K, OsFER2; L, OsIRO2; M, OsYSL2; and N, OsFRDL1) related to Fe3+ absorption and transport in WT and osacl-a2 treated with the indicated exogenous Fe3+ concentrations at two weeks after germination. Ubiquitin (LOC_Os06g46770) was used as the internal control. Data in C-E and H-J are mean ± SE (n = 3). ** indicates significant differences at the 0.01 level by Student’s t-test.In K-N, different lowercase letters above bars indicate significant differences at P < 0.05 by Tukey’s multiple comparisons test.

Fig. 2. OsACL-A2 dependent iron uptake positively affects disease resistance. A, Spray inoculation of wild type (WT) ZH8015 and osacl-a2 (treated with the indicated exogenous iron concentrations at two weeks after germination) with Magnaporthe oryzae strain 14-1. Leaves were photographed at 7 d post-inoculation. Scale bars, 2 cm. S-Fe3+, Starvation (0 μmol/L Fe3+); N-Fe3+, Normal (50 μmol/L Fe3+); E-Fe3+, Excess (500 μmol/L Fe3+). B, Relative fungal growth in the first leaf from the top. C, Number of different lesion types in the leaf. D, Transcript levels of OsACL-A2 in WT leaves with (14-1 strain) and without (Mock) M. oryzae infection. LOC_Os03g50885 was used as the internal control. E and F, ACL activity (E) and citric acid content (F) in WT after M. oryzae infection. Data are mean ± SE (n = 5 in B and C; n = 3 in D-F). Different lowercase letters above bars indicate significant differences at P < 0.05 level by Tukey’s multiple comparisons test.

Fig. 2. OsACL-A2 dependent iron uptake positively affects disease resistance. A, Spray inoculation of wild type (WT) ZH8015 and osacl-a2 (treated with the indicated exogenous iron concentrations at two weeks after germination) with Magnaporthe oryzae strain 14-1. Leaves were photographed at 7 d post-inoculation. Scale bars, 2 cm. S-Fe3+, Starvation (0 μmol/L Fe3+); N-Fe3+, Normal (50 μmol/L Fe3+); E-Fe3+, Excess (500 μmol/L Fe3+). B, Relative fungal growth in the first leaf from the top. C, Number of different lesion types in the leaf. D, Transcript levels of OsACL-A2 in WT leaves with (14-1 strain) and without (Mock) M. oryzae infection. LOC_Os03g50885 was used as the internal control. E and F, ACL activity (E) and citric acid content (F) in WT after M. oryzae infection. Data are mean ± SE (n = 5 in B and C; n = 3 in D-F). Different lowercase letters above bars indicate significant differences at P < 0.05 level by Tukey’s multiple comparisons test.

参考文献 20

[1] Cao M, Platre M P, Tsai H H, et al. 2024. Spatial IMA1 regulation restricts root iron acquisition on MAMP perception. Nature, 625: 750-759.
[2] Conrad M, Kagan V E, Bayir H, et al. 2018. Regulation of lipid peroxidation and ferroptosis in diverse species. Genes Dev, 32(9/10): 602-619.
[3] Dangol S, Chen Y F, Hwang B K, et al. 2019. Iron- and reactive oxygen species-dependent ferroptotic cell death in rice-Magnaporthe oryzae interactions. Plant Cell, 31(1): 189-209.
[4] Distéfano A M, López G A, Setzes N, et al. 2021. Ferroptosis in plants: Triggers, proposed mechanisms, and the role of iron in modulating cell death. J Exp Bot, 72(6): 2125-2135.
[5] Herlihy J H, Long T A, McDowell J M. 2020. Iron homeostasis and plant immune responses: Recent insights and translational implications. J Biol Chem, 295(39): 13444-13457.
[6] Huang S, Yamaji N, Ma J F. 2024. Metal transport systems in plants. Annu Rev Plant Biol, 75(1): 1-25.
[7] Kobayashi T, Nagano A J, Nishizawa N K. 2021. Iron deficiency-inducible peptide-coding genes OsIMA1 and OsIMA2 positively regulate a major pathway of iron uptake and translocation in rice. J Exp Bot, 72(6): 2196-2211.
[8] Li C Y, Li Y, Xu P, et al. 2022. OsIRO3 negatively regulates Fe homeostasis by repressing the expression of OsIRO2. Plant J, 111(4): 966-978.
[9] Müller B, Kovács K, Pham H D, et al. 2019. Chloroplasts preferentially take up ferric-citrate over iron-nicotianamine complexes in Brassica napus. Planta, 249(3): 751-763.
[10] Nguyen N K, Wang J, Liu D P, et al. 2022. Rice iron storage protein ferritin 2 (OsFER2) positively regulates ferroptotic cell death and defense responses against Magnaporthe oryzae. Front Plant Sci, 13: 1019669.
[11] Ruan B P, Hua Z H, Zhao J, et al. 2019. OsACL-A2 negatively regulates cell death and disease resistance in rice. Plant Biotechnol J, 17(7): 1344-1356.
[12] Solti Á, Kovács K, Basa B, et al. 2012. Uptake and incorporation of iron in sugar beet chloroplasts. Plant Physiol Biochem, 52: 91-97.
[13] Sun J Y, Zhou Z R, Wang Y Q, et al. 2024. OsHRZ1 negatively regulates rice resistant to Magnaporthe oryzae infection by targeting OsVOZ2. Transgenic Res, 33(5): 489-501.
[14] Wu T Y, Gruissem W, Bhullar N K. 2018. Facilitated citrate-dependent iron translocation increases rice endosperm iron and zinc concentrations. Plant Sci, 270: 13-22.
[15] Xu Z N, Zhou Z Q, Cheng Z X, et al. 2023. A transcription factor ZmGLK36 confers broad resistance to maize rough dwarf disease in cereal crops. Nat Plants, 9(10): 1720-1733.
[16] Yamaji N, Yoshioka Y, Huang S, et al. 2024. An oligo peptide transporter family member, OsOPT7, mediates xylem unloading of Fe for its preferential distribution in rice. New Phytol, 242(6): 2620-2634.
[17] Yang S Q, Chen N N, Qi J X, et al. 2024. OsUGE2 regulates plant growth through affecting ROS homeostasis and iron level in rice. Rice, 17(1): 6.
[18] Yokosho K, Yamaji N, Ueno D, et al. 2009. OsFRDL1 is a citrate transporter required for efficient translocation of iron in rice. Plant Physiol, 149(1): 297-305.
[19] Yokosho K, Yamaji N, Ma J F. 2016. OsFRDL1 expressed in nodes is required for distribution of iron to grains in rice. J Exp Bot, 67(18): 5485-5494.
[20] Zhu X B, Ze M, Chern M, et al. 2020. Deciphering rice lesion mimic mutants to understand molecular network governing plant immunity and growth. Rice Sci, 27(4): 278-288.

相关文章 0

No related articles found!

编辑推荐

Metrics

阅读次数
全文


摘要

  • 摘要
  • 图/表
  • 参考文献
  • 相关文章
  • 编辑推荐
  • Metrics
回顶部
浙ICP备05004719号-15   公安备案号:33010302003355
版权所有 © 《Rice Science》编辑部
地址:浙江省杭州市体育场路359号 邮编:310006 电话:0571-63371017 E-mail:crrn@fy.hz.zn.cn; cjrs278@gmail.com
本系统由北京玛格泰克科技发展有限公司设计开发
总访问量: 今日访问: 在线人数: