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Genomic and Transcriptomic Insights into Stage-Specific Drought Resilience in Diverse Myanmar Rice Germplasm. 基因组学和转录组学研究缅甸不同水稻种质的阶段特异性抗旱能力。
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-30 DOI: 10.1186/s12284-025-00877-2
Nant Nyein Zar Ni Naing, Chunli Wang, Qian Zhu, Honghai Yan, Cui Zhang, Junjie Li, Xianyu Wang, Dandan Li, Jiancheng Wen, Chengyun Li, Youyong Zhu, Lijuan Chen, Dongsun Lee
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引用次数: 0
Engineering non-coding DNA Elements in Rice: an Elegant Approach To fine-tune Agronomical Advantageous Traits. 水稻工程非编码DNA元件:一种微调农艺优势性状的优雅方法。
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-29 DOI: 10.1186/s12284-025-00846-9
Tilak Chandra, Sarika Jaiswal, Kutubuddin A Molla, Deependra Pratap Singh, Mir Asif Iquebal, Dinesh Kumar

Rice serves as a fundamental staple crop, supporting the dietary needs of nearly one-third of the global population. This critical role necessitates immediate and strategic efforts to develop multi-attribute genotypes to ensure sustainable food and nutritional security for the burgeoning population. The augmentation of rice production is not only vital for addressing immediate food demands but also crucial for fostering long-term sustainability, thereby supporting livelihoods and driving economic development. Achieving this transformation necessitates a holistic and systems-level understanding of the molecular and regulatory networks that govern phenotypic plasticity and agronomic performance. While coding regions are pivotal for expression, non-coding elements play an even more prominent role in regulating transcriptional activity and orchestrating essential biological processes. Natural allelic variation within these non-coding elements serves as an evolutionary substrate for regulatory rewiring, contributing to adaptive plasticity, domestication traits, and intraspecific diversification. Therefore, the precise modulation of desirable agronomic traits could be facilitated by targeted engineering of such elements, which often allows for the fine-tuning of allelic effects in terms of the attenuation and partial restoration of alleles to impact desirable traits over coding components, which often results in complete exclusion or lethality. Therefore, we attempted to provide a comprehensive synthesis of functionally characterized non-coding elements exclusively for rice, highlight their functional roles, and emphasize how natural variation within these elements is critical for selecting traits associated with domestication and the breeding of elite genotypes. Notably, the potential of engineered non-coding RNA elements for the enhancement of agronomically advantageous traits is critically discussed. The future roadmap of non-coding element editing in rice is expected to be significantly shaped by continuous technological innovations in the editing toolbox, coupled with breakthrough discoveries for non-coding elements influencing agronomical traits. These advances have the potential to revolutionize the development of superior rice genotypes, ultimately contributing to the global effort to ensure food and nutritional security.

大米是一种基本的主食作物,满足了全球近三分之一人口的饮食需求。这一关键作用需要立即作出战略性努力,开发多属性基因型,以确保为迅速增长的人口提供可持续的粮食和营养安全。提高水稻产量不仅对解决眼前的粮食需求至关重要,而且对促进长期可持续性至关重要,从而支持生计和推动经济发展。实现这一转变需要对控制表型可塑性和农艺性能的分子和调控网络有一个整体和系统级的理解。虽然编码区对表达至关重要,但非编码元件在调节转录活性和协调基本生物过程中发挥的作用更为突出。这些非编码元件中的自然等位基因变异是调控重布线的进化基础,有助于适应性可塑性、驯化特性和种内多样化。因此,理想农艺性状的精确调节可以通过这些元件的靶向工程来促进,这通常允许在等位基因的衰减和部分恢复方面对等位基因效应进行微调,从而影响编码成分的理想性状,这通常导致完全排除或致命。因此,我们试图提供一个功能特征的非编码元件的综合,突出它们的功能作用,并强调这些元件的自然变异是如何选择与驯化和精英基因型育种相关的性状的关键。值得注意的是,工程非编码RNA元件在增强农艺优势性状方面的潜力进行了批判性讨论。随着编辑工具箱的不断技术创新,以及对影响农艺性状的非编码元素的突破性发现,未来水稻非编码元素编辑的路线图有望得到显著塑造。这些进展有可能彻底改变优良水稻基因型的开发,最终为确保粮食和营养安全的全球努力作出贡献。
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引用次数: 0
Rice OsFKF1 Promotes Degradation of OsPRR37 for Short-Day Early Flowering. 水稻OsFKF1促进OsPRR37短日早花降解
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-26 DOI: 10.1186/s12284-025-00880-7
Hyeryung Yoon, Sang-Ji Lee, Jinku Kang, Sung-Hwan Cho, Nam-Chon Paek
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引用次数: 0
Integrating Multi-omics Analysis to Decipher the Genetic Basis of Heterosis in Xieyou9308. 整合多组学分析解读协优9308杂种优势遗传基础。
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-24 DOI: 10.1186/s12284-025-00875-4
Feng Lin, Tainle Zhu, Muhammad Kamran, Xiong Zheng, Mingzhe Suo, Haiming Xu, Liyong Cao, Yongbo Hong

The intersubspecific rice hybrid Xieyou9308 exhibits striking hybrid vigor and serves as a valuable resource for dissecting the genetic basis of yield heterosis in indica-japonica crosses. However, the molecular mechanisms underlying this hybrid vigor remain poorly understood. Leveraging a set of recombinant inbred lines (RILs) and an immortalized F2 (IMF2) population derived from Xieyou9308, 1,300,425 genomic variants were identified, which were consolidated into 3818 BIN markers. Genomic regions inherited from Zhonghui9308 were positively associated with traits including plant height, heading date, panicle length, and grain number per panicle. In contrast, regions derived from XieqingzaoB, particularly those located on chromosome 3, positively associated with grain length and 1000-grain weight. In the RIL population, 43 additive QTLs and 3 pairs of epistatic QTLs were identified for 10 agronomic traits, with the majority mapped to chromosomes 3 and 10, which harbor candidate genes including Ehd1, GS3, and OsTB1. In the IMF2 population, 118 significant QTLs exhibiting partial dominance and 11 epistatic interactions were identified, underscoring the contributions of both partial dominance and epistasis to trait expression. Transcriptomic analysis further corroborated these findings, showing that alleles predominantly from Zhonghui9308 contributed to a prolonged growth duration, while those from XieqingzaoB shortened the growth duration. Collectively, these findings indicate that the hybrid vigor exhibited in Xieyou9308 is attributable to the synergistic effects of superior parental alleles and their epistatic interactions. These insights offer a valuable foundation for molecular breeding strategies aimed at improving yield in indica-japonica hybrid rice.

亚种间水稻杂交种协优9308表现出显著的杂交活力,为剖析籼粳杂交产量杂种优势的遗传基础提供了宝贵的资源。然而,这种杂交活力背后的分子机制仍然知之甚少。利用一组重组自交系(RILs)和一个来自协优9308的永生化F2 (IMF2)群体,鉴定了1,300,425个基因组变异,并将其整合到3818个BIN标记中。中恢9308遗传的基因组区域与株高、抽穗日期、穗长、每穗粒数等性状呈正相关。与此相反,谢青藻b衍生的区域,特别是位于3号染色体上的区域,与粒长和千粒重呈正相关。在RIL群体中,共鉴定出10个农艺性状的43个加性qtl和3对上位性qtl,其中大部分定位在3号和10号染色体上,其中包含候选基因包括Ehd1、GS3和OsTB1。在IMF2群体中,鉴定出118个显著的部分显性qtl和11个上位互作qtl,强调了部分显性和上位互作对性状表达的贡献。转录组学分析进一步证实了这些发现,表明中恢9308的等位基因对延长生育期有贡献,协青藻b的等位基因对缩短生育期有贡献。综上所述,协优9308表现出的杂种优势是亲本优势等位基因的协同作用及其上位互作的结果。这些发现为提高籼粳杂交稻产量的分子育种策略提供了有价值的基础。
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引用次数: 0
Natural Variation in the Promoter of OsMOT1;1 Contributes to Differential Molybdenum Accumulation between Indica and Japonica Rice. OsMOT1启动子的自然变异1对籼稻和粳稻的钼积累差异有贡献。
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-24 DOI: 10.1186/s12284-025-00876-3
Pengyuan Guo, Lingyue Zhang, Qingqing Du, Lei Huang, Fangchi Wei, Zongyue Jiang, Zihan Zhao, Mengfan Liu, Kangshun Huang, Fugang Huang, Weiwei Gao, Xingming Lian, Meng Yang
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引用次数: 0
SQUAMOSA-Promoter Binding Protein Like 10/14 (OsSPL10/14) Regulate Salt Tolerance by Modulating Reactive Oxygen Species Homeostasis in Rice (Oryza Sativa L.). squamosa -启动子结合蛋白样10/14 (OsSPL10/14)通过调控水稻活性氧稳态调控耐盐性。
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-22 DOI: 10.1186/s12284-025-00878-1
Chaowei Fang, Yuanqing Nie, Minglan Zhu, Xinyi Yu, Liwen Jia, Jiayi Li, Xin Shu, Taotao Zhu, Weihong Liang

Soil salinization seriously impacts the growth and development, yield, and grain quality of crops. Elucidating the molecular underlying of salt tolerance is crucial for advancing stress-resistant molecular breeding research in crops. Here, we identified a salt stress-responsive gene, SQUAMOSA-promoter binding protein like 10 (OsSPL10), and characterized its molecular function in conferring salt tolerance to rice. Firstly, we generated and characterized three distinct types of spl10 mutants using CRISPR/Cas9 mutagenesis. In spl10 mutant, the leaf withered rate was lower than that in wild type (WT), the plant height and fresh weight per plant of spl10 were higher than WT under salt stress, indicating that spl10 exhibits tolerance to salt stress. Based on biochemical and physiological assays, the OsSPL10/14 complex was identified as a key regulator of salt stress response in rice by modulating the homeostasis of reactive oxygen species (ROS). Besides, the RNA-Seq assay confirmed that OsSPL10 may be involved in plant hormone signal transduction and phenylpropanoid biosynthesis pathways under salt stress, providing valuable insights for exploring the downstream target genes of OsSPL10. These findings offer novel insights into the molecular mechanisms underlying salt tolerance mediated by the SPL transcription factor in plants.

土壤盐渍化严重影响作物的生长发育、产量和籽粒品质。阐明作物耐盐性的分子基础,对推进作物抗逆性分子育种研究具有重要意义。本研究鉴定了一个盐胁迫响应基因——SQUAMOSA-promoter binding protein like 10 (OsSPL10),并鉴定了其在水稻耐盐性中的分子功能。首先,我们利用CRISPR/Cas9诱变技术产生并鉴定了三种不同类型的spl10突变体。在盐胁迫下,spl10突变体叶片干枯率低于野生型,株高和单株鲜重均高于野生型,表明spl10具有耐盐性。基于生化和生理分析,OsSPL10/14复合体通过调节活性氧(ROS)的稳态,被鉴定为水稻盐胁迫响应的关键调控因子。此外,RNA-Seq分析证实OsSPL10可能参与盐胁迫下植物激素信号转导和苯丙素生物合成途径,为探索OsSPL10的下游靶基因提供了有价值的见解。这些发现为SPL转录因子介导植物耐盐性的分子机制提供了新的见解。
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引用次数: 0
OsSSID6 Negatively Regulates Salt Stress Tolerance in Rice (Oryza Sativa L.) via Metabolic Pathways and ROS Scavenging. OsSSID6通过代谢途径和活性氧清除负调控水稻耐盐性。
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-15 DOI: 10.1186/s12284-025-00868-3
Ziyi Wang, Xiaofei Zan, Hao Chen, Jiali Zhu, Xiulin Zhao, Mingfei Chen, Yijuan Kong, Juan Yang, Xiaomei Jia, Xiaoying Ye, Chuanqiang Liu, Rongjun Chen, Jianqing Zhu, Jun Zhu, Lihua Li

Soil salinization is becoming a huge threat to reducing productivity of rice (Oryza sativa L.) around the world. Previous studies have found that some Domain of unknown function (DUF) proteins play an essential role in the growth and development of plants. The DUF936 family is reported to respond to abiotic stresses, but the specific molecular mechanisms of its members remain elusive. In this study, OsSSID6 (Salt-Stress Induced DUF936 protein) is found at the cell membrane and the protein's expression could be affected by several abiotic stresses. The CRISPR/Cas9 knockout lines increased salt tolerance in rice, whereas the overexpression lines showed more sensitivity. And meanwhile the similar changes of ROS-scavenging capacity were observed both in knockout and overexpression lines. Transcriptome analysis identified that the expression of genes linked to multiple metabolic pathways, including phenylpropanoid and flavonoid biosynthesis, and stress response, was significantly up-regulated in KO lines. Our findings reveal that OsSSID6 gene modulates rice salt stress tolerance by orchestrating a network of metabolic pathways, including those involved in the reactive oxygen species (ROS) scavenging system, phenylpropanoid and flavonoid biosynthesis and stress response-related mechanism. sThese results provide important information for engineering salt-tolerant crops.

在世界范围内,土壤盐碱化正成为水稻生产力下降的巨大威胁。已有研究发现,一些未知功能域(DUF)蛋白在植物的生长发育中起着至关重要的作用。据报道,DUF936家族对非生物胁迫有反应,但其成员的具体分子机制尚不清楚。本研究在细胞膜上发现了盐胁迫诱导DUF936蛋白OsSSID6 (Salt-Stress Induced DUF936 protein),该蛋白的表达会受到多种非生物胁迫的影响。CRISPR/Cas9敲除系提高了水稻的耐盐性,而过表达系表现出更强的敏感性。同时,基因敲除系和过表达系的ros清除能力也发生了类似的变化。转录组分析发现,与苯丙素和类黄酮生物合成以及应激反应等多种代谢途径相关的基因表达在KO系中显著上调。研究结果表明,OsSSID6基因通过调控一系列代谢途径,包括活性氧(ROS)清除系统、苯丙素和类黄酮的生物合成以及胁迫反应相关机制,调控水稻耐盐性。这些结果为工程种植耐盐作物提供了重要信息。
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引用次数: 0
Different Substrates Drive Differential Responses of Rice to Salt Stress. 不同基质驱动水稻对盐胁迫的不同响应。
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-13 DOI: 10.1186/s12284-025-00857-6
Hang Zhou, Naijie Feng, Dianfeng Zheng, Zhaohui Wu

Studying the salt tolerance mechanisms of rice under a single substrate has certain limitations. The salt tolerance strategies of rice may differ under different substrate conditions. This study established three substrate types by adjusting the proportions of laterite, peat moss, and river sand: S1 (high sand; low nutrient), S2 (medium sand; medium nutrient), and S3 (low sand; high nutrient). Compared with the respective fresh water control, the magnitude of dry weight reduction in each substrate gradually decreased (S1-S3), indicating that the salt stress was effectively alleviated. KEGG enrichment analysis of differentially expressed genes (DEGs) showed that Xiangliangyou900 may be more dependent on the remodeling of carbon metabolism pathway (compared to nitrogen metabolism) in S1, but the nitrogen metabolism pathway were more significant in S3. In S3, differential metabolites were significantly enriched in carbon and nitrogen metabolism pathways, but no such enrichment was found in S1, indicating that the S3 substrate, with its high nutrient and low river sand content, is more likely to trigger carbon and nitrogen metabolism remodeling. Under salt stress, the methylation level of C bases in the CHH type increased in S1 and decreased in S3. The methylation level of CHH-type C bases in the whole genome was more strongly correlated with the physicochemical parameters of the substrate (compared to CG and CHG types).This study speculated that rice may optimize its ability to adapt to salt stress by specifically regulating the methylation of CHH-type C bases to mediate gene expression. The results of this study help enrich the theoretical system of the rice salt stress response mechanism.

研究单一基质条件下水稻耐盐机理具有一定的局限性。不同基质条件下,水稻的耐盐策略不同。本研究通过调整红土、泥炭苔藓和河砂的比例,建立了3种基质类型:S1(高沙、低营养)、S2(中沙、中营养)和S3(低沙、高营养)。与淡水对照相比,各基质干重减少幅度逐渐减小(s1 ~ s3),表明盐胁迫得到有效缓解。差异表达基因(DEGs)的KEGG富集分析表明,与氮代谢相比,香两优900在S1中可能更依赖于碳代谢途径的重塑,而在S3中氮代谢途径的重塑更为显著。在S3中,碳氮代谢途径的差异代谢物显著富集,但在S1中没有发现这种富集,说明S3底物营养高、河砂含量低,更容易引发碳氮代谢重塑。盐胁迫下,CHH型C碱基甲基化水平在S1期升高,在S3期降低。与CG和CHG型相比,全基因组中chh型C碱基的甲基化水平与底物的理化参数相关性更强。本研究推测,水稻可能通过特异性调节CHH-type C碱基甲基化介导基因表达来优化其适应盐胁迫的能力。本研究结果有助于丰富水稻盐胁迫响应机制的理论体系。
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引用次数: 0
OsnTNB.11 Encodes a CC-NBS-LRR Type Resistance Protein that Positively Regulates Resistance to Rice Kernel Smut by Modulating the Ethylene Signalling. OsnTNB.11编码一种CC-NBS-LRR型抗性蛋白,通过调节乙烯信号正向调节水稻黑穗病抗性。
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-12 DOI: 10.1186/s12284-025-00874-5
Xinyue Shu, Desuo Yin, Aiping Zheng, Aijun Wang
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引用次数: 0
Correction: Exogenous Calcium-Mediated Reinforcement of Cell Wall Represents a Pivotal Mechanism in Rice's Primed Defense Response Against Brown Planthopper Reproduction. 更正:外源钙介导的细胞壁强化是水稻抵御褐飞虱繁殖的启动防御反应的关键机制。
IF 5 1区 农林科学 Q1 AGRONOMY Pub Date : 2025-12-10 DOI: 10.1186/s12284-025-00867-4
Xiao Liu, Zhongyan Zhu, Lina Chen, Jing Xie, Qiyao Mo, Mao Ye
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引用次数: 0
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