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Rice Science ›› 2026, Vol. 33 ›› Issue (1): 1-4.DOI: 10.1016/j.rsci.2025.10.011

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  • 收稿日期:2025-07-29 接受日期:2025-10-28 出版日期:2026-01-28 发布日期:2026-02-03

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. [J]. Rice Science, 2026, 33(1): 1-4.

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链接本文: http://www.ricesci.org/CN/10.1016/j.rsci.2025.10.011

               http://www.ricesci.org/CN/Y2026/V33/I1/1

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Fig. 1. Phenotypic, histological, and transcriptional analyses of wild-type (WT) and ossp3 mutant plants. A, Root characterization of WT, ossp3-1, and ossp3-2 over 10 d post-germination. From left to right at each time point are WT, ossp3-1, and ossp3-2. Scale bar, 1 cm. B, Primary root length of WT, ossp3-1, and ossp3-2 over 10 d post-germination. Data are mean ± SD (n = 15). C, Number of lateral roots of WT, ossp3-1, and ossp3-2 over 10 d post-germination. Data are mean ± SD (n = 15). D, Angles of lateral roots of WT, ossp3-1, and ossp3-2 at 6‒13 d post-germination. Bar chart shows lateral root angle; circles indicate differences in lateral root angles. Data are mean ± SD (n = 15). E, Transverse sections of the elongation zone of WT and ossp3-1. Scale bar, 50 μm. F, Diameter of the elongation zone of WT and ossp3-1. Data are mean ± SD (n = 3). G, Longitudinal sections of the elongation zone of WT and ossp3-1. Scale bar, 50 μm. H, Cell length and width in the elongation zone of WT and ossp3-1. Data are mean ± SD (n = 50). I, Yeast two-hybrid assay between OsSP3 and LEA5. Yeast transformants were spotted onto medium (SD/‐Leu/‐Trp) and selective medium (SD/‐Leu/‐Trp/‐His/‐Ade) supplemented with X‐α‐gal. Serial dilutions (1, 0.1, and 0.01) were applied on the selective medium. J, Bimolecular fluorescence complementation (BiFC) assay between OsSP3 and LEA5 in Nicotiana benthamiana. cYFP, C-terminal yellow fluorescent protein; nYFP, N-terminal yellow fluorescent protein. H2B-mCherry labels the nucleus. Scale bars, 20 μm. K, Split-luciferase (LUC) assays between OsSP3 and LEA5 and controls. cLUC, C-terminal LUC; nLUC, N-terminal LUC. L, Subcellular localization of LEA5 in Nicotiana benthamiana leaf cells and rice protoplasts. H2B-mCherry labels the nucleus. GFP, Green fluorescent protein. Scale bars in upper and lower panels are 50 μm and 5 μm, respectively. M, OsSP3 and LEA5 expression by qRT-PCR. Panicle and root samples were collected at the young panicle differentiation stage with three biological replicates. OsActin (Os03g0718100) was used as an internal reference. Data are mean ± SD (n = 3). * and ** indicate significant differences at P < 0.05 and P < 0.01, respectively, by Student’s t-test.

Fig. 1. Phenotypic, histological, and transcriptional analyses of wild-type (WT) and ossp3 mutant plants. A, Root characterization of WT, ossp3-1, and ossp3-2 over 10 d post-germination. From left to right at each time point are WT, ossp3-1, and ossp3-2. Scale bar, 1 cm. B, Primary root length of WT, ossp3-1, and ossp3-2 over 10 d post-germination. Data are mean ± SD (n = 15). C, Number of lateral roots of WT, ossp3-1, and ossp3-2 over 10 d post-germination. Data are mean ± SD (n = 15). D, Angles of lateral roots of WT, ossp3-1, and ossp3-2 at 6‒13 d post-germination. Bar chart shows lateral root angle; circles indicate differences in lateral root angles. Data are mean ± SD (n = 15). E, Transverse sections of the elongation zone of WT and ossp3-1. Scale bar, 50 μm. F, Diameter of the elongation zone of WT and ossp3-1. Data are mean ± SD (n = 3). G, Longitudinal sections of the elongation zone of WT and ossp3-1. Scale bar, 50 μm. H, Cell length and width in the elongation zone of WT and ossp3-1. Data are mean ± SD (n = 50). I, Yeast two-hybrid assay between OsSP3 and LEA5. Yeast transformants were spotted onto medium (SD/‐Leu/‐Trp) and selective medium (SD/‐Leu/‐Trp/‐His/‐Ade) supplemented with X‐α‐gal. Serial dilutions (1, 0.1, and 0.01) were applied on the selective medium. J, Bimolecular fluorescence complementation (BiFC) assay between OsSP3 and LEA5 in Nicotiana benthamiana. cYFP, C-terminal yellow fluorescent protein; nYFP, N-terminal yellow fluorescent protein. H2B-mCherry labels the nucleus. Scale bars, 20 μm. K, Split-luciferase (LUC) assays between OsSP3 and LEA5 and controls. cLUC, C-terminal LUC; nLUC, N-terminal LUC. L, Subcellular localization of LEA5 in Nicotiana benthamiana leaf cells and rice protoplasts. H2B-mCherry labels the nucleus. GFP, Green fluorescent protein. Scale bars in upper and lower panels are 50 μm and 5 μm, respectively. M, OsSP3 and LEA5 expression by qRT-PCR. Panicle and root samples were collected at the young panicle differentiation stage with three biological replicates. OsActin (Os03g0718100) was used as an internal reference. Data are mean ± SD (n = 3). * and ** indicate significant differences at P < 0.05 and P < 0.01, respectively, by Student’s t-test.

参考文献 14

[1] Carrillo-Carrasco V P, Hernandez-Garcia J, Mutte S K, et al. 2023. The birth of a giant: Evolutionary insights into the origin of auxin responses in plants. EMBO J, 42(6): e113018.
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[3] Geng L P, Li Q, Jiao L L, et al. 2023. WOX11 and CRL1 act synergistically to promote crown root development by maintaining cytokinin homeostasis in rice. New Phytol, 237(1): 204-216.
[4] Huang L P, Jia J, Zhao X X, et al. 2018. The ascorbate peroxidase APX1 is a direct target of a zinc finger transcription factor ZFP36 and a late embryogenesis abundant protein OsLEA 5 interacts with ZFP36 to co-regulate OsAPX1 in seed germination in rice. Biochem Biophys Res Commun, 495(1): 339-345.
[5] Huang Y S, Dong H, Mou C L, et al. 2022. Ribonuclease H-like gene SMALL GRAIN2 regulates grain size in rice through brassinosteroid signaling pathway. J Integr Plant Biol, 64(10): 1883-1900.
[6] Inukai Y, Sakamoto T, Ueguchi-Tanaka M, et al. 2005. Crown rootless1, which is essential for crown root formation in rice, is a target of an AUXIN RESPONSE FACTOR in auxin signaling. Plant Cell, 17(5): 1387-1396.
[7] Kitomi Y, Ito H, Hobo T, et al. 2011. The auxin responsive AP2/ERF transcription factor CROWN ROOTLESS5 is involved in crown root initiation in rice through the induction of OsRR1, a type-A response regulator of cytokinin signaling. Plant J, 67(3): 472-484.
[8] Li H, Sun H Y, Jiang J H, et al. 2021. TAC4 controls tiller angle by regulating the endogenous auxin content and distribution in rice. Plant Biotechnol J, 19(1): 64-73.
[9] Liu Y Y, He C Y, Gai D S, et al. 2022. Morphological and physiological traits of roots and their relationships with shoot growth and grain yield in direct-seeded rice in northeastern China. Crop Pasture Sci, 73(11): 1229-1244.
[10] Singh Z, Singh H, Garg T, et al. 2023. Genetic and hormonal blueprint of shoot-borne adventitious root development in rice and maize. Plant Cell Physiol, 63(12): 1806-1813.
[11] Uga Y, Sugimoto K, Ogawa S, et al. 2013. Control of root system architecture by DEEPER ROOTING 1 increases rice yield under drought conditions. Nat Genet, 45(9): 1097-1102.
[12] Ye J, Ye S H, Zeng W, et al. 2025. Mutation of short panicle gene 3 caused shorter panicle through auxin and cytokinin pathway in rice. J Plant Growth Regul, 44(2): 988-998.
[13] Zhang H, Xue Y G, Wang Z Q, et al. 2009. Morphological and physiological traits of roots and their relationships with shoot growth in ‘super’ rice. Field Crops Res, 113(1): 31-40.
[14] Zhao Y, Hu Y F, Dai M Q, et al. 2009. The WUSCHEL-related homeobox gene WOX11 is required to activate shoot-borne crown root development in rice. Plant Cell, 21(3): 736-748.

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