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学者姓名：贾琪
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Abstract ：
Evidence suggests that the metabolism of inositol and its derivatives may be involved in various biological processes including salt tolerance, but there has been limited understanding. Ectopic expression of Gs5PTase8, an inositol polyphosphate 5-phosphatase cloned from wild soybean (Glycine soja), significantly enhanced salt tolerance in cultivated soybean (Glycine max). In this follow up study, the overexpression of Gs5PTase8 was shown to improve salt tolerance in transgenic Arabidopsis thaliana, soybean hairy roots and composite plants, by preventing sodium (Na+) accumulation and maintaining lower sodium/potassium (Na+/K+) ratios in plants under salt stress. Additionally, the interactions between Gs5PTase8 and its substrate, inositol 1,4,5-trisphosphate (IP3), were investigated for their role in enhancing salt tolerance. Overexpressing Gs5PTase8 reduced IP3 contents, probably due to its 5-phosphatase activity. Moreover, external supplementation of IP3 could restore the Na+ accumulation in the Gs5PTase8-overexpressing tobacco BY-2 cells experiencing salt stress. The proteomic data obtained by data-independent acquisition implied that the degradation of IP3 or phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) by Gs5PTase8 may maintain the ion homoeostasis of plants under salt stress by influencing the cytosolic calcium (Ca2+) signalling and the salt overly sensitive pathways.
Keyword ：
calcium (Ca2+) signalling calcium (Ca2+) signalling inositol 1,4,5-trisphosphate (IP3) inositol 1,4,5-trisphosphate (IP3) inositol polyphosphate 5-phosphatase (5PTase) inositol polyphosphate 5-phosphatase (5PTase) salt overly sensitive (SOS) salt overly sensitive (SOS) salt tolerance salt tolerance sodium (Na plus ) accumulation sodium (Na plus ) accumulation soybean soybean
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| GB/T 7714 | Jia, Qi , Chen, Yuan , Kong, Defeng et al. Soybean Inositol Polyphosphate 5-Phosphatase 8 Confers Salt Tolerance by Reducing Sodium Influx Through Inositol 1,4,5-Trisphosphate Signalling [J]. | PLANT CELL AND ENVIRONMENT , 2025 . |
| MLA | Jia, Qi et al. "Soybean Inositol Polyphosphate 5-Phosphatase 8 Confers Salt Tolerance by Reducing Sodium Influx Through Inositol 1,4,5-Trisphosphate Signalling" . | PLANT CELL AND ENVIRONMENT (2025) . |
| APA | Jia, Qi , Chen, Yuan , Kong, Defeng , Fan, Hanyu , Sun, Song , Liu, Yuhang et al. Soybean Inositol Polyphosphate 5-Phosphatase 8 Confers Salt Tolerance by Reducing Sodium Influx Through Inositol 1,4,5-Trisphosphate Signalling . | PLANT CELL AND ENVIRONMENT , 2025 . |
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植物F-box蛋白MAX2是独角金内酯(strigolactones, SLs)和烟素(karrinkins, KARs)信号传导的关键作用因子，作为SKP1-CUL1-FBX(SCF)复合体型泛素连接酶E3的主要成分，负责特异性识别并介导靶蛋白SMAX1/SMXLs的泛素化降解，从而调控植物形态建成和抗逆反应。重要粮油作物大豆(Glycine max)中亦存在MAX2的同源基因，然而其在植物防御反应中的功能却尚未被解析。为研究大豆中MAX2的同源基因的功能，本研究在生长受胁迫的大豆中成功克隆得到MAX2的同源基因GmMAX2b。生物信息学分析表明大豆存在2个MAX2同源基因GmMAX2a和GmMAX2b，相似度达96.2%,F-box区段高度保守。植物MAX2同源物蛋白序列比对及聚类分析基本反应了植物进化的亲缘关系，也提示大豆MAX2可能是多功能蛋白。表达分析表明，与拟南芥MAX2类似，植物病原菌侵染和水杨酸处理均能诱导大豆GmMAX2b表达。异位表达GmMAX2b能够回补max2-2突变体的感病性，说明GmMAX2b对植物抗病反应有正调节功能。此外，采用酵母双杂技术探寻GmMAX2b潜在的互作靶蛋白，发现其与SMXL6互作，与SMXL2存在微弱互作。这表明GmMAX2b是防御反应中正调控因子，受病原菌侵染和水杨酸处理诱导表达，其可能通过与SMXL6和SMXL2互作而发挥作用。本研究拓展了对大豆抗病F-box的理论认知，为今后大豆抗病育种提供了科学依据。
Keyword ：
GmMAX2b GmMAX2b 基因克隆 基因克隆 大豆 大豆 植物抗病反应 植物抗病反应
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| GB/T 7714 | 傅嘉辉 , 左林 , 黄伟群 et al. 大豆GmMAX2b基因克隆及抗病功能分析 [J]. | 生物工程学报 , 2025 , 41 (07) : 2803-2817 . |
| MLA | 傅嘉辉 et al. "大豆GmMAX2b基因克隆及抗病功能分析" . | 生物工程学报 41 . 07 (2025) : 2803-2817 . |
| APA | 傅嘉辉 , 左林 , 黄伟群 , 孙松 , 郭良雨 , 胡闽 et al. 大豆GmMAX2b基因克隆及抗病功能分析 . | 生物工程学报 , 2025 , 41 (07) , 2803-2817 . |
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Cotton diseases pose a serious threat to yield and fiber quality. Systemic acquired resistance (SAR) is a crucial and prolonged immune response to pathogen infection; yet, its regulatory mechanisms remain poorly understood in cotton. Here, 35 TGACG binding (TGA) transcription factors were identified in Gossypium hirsutum, classifying them into five groups based on phylogenetic analysis, conserved motifs, and gene structures. Among them, GhTGA12, a group II member, emerged as a novel disease-associated transcription factor based on RNA-seq analysis under biotic stress conditions. GhTGA12 encodes a nuclear protein with 11 exons and 10 introns, harboring the conserved TGA-specific domains (bZIP, DOG1, Q1, and Q2). GhTGA12 has transcriptional activation activity through its N-terminal region and could be triggered by Pst DC3000. While GhTGA12-over-expressing Arabidopsis did not exhibit enhanced resistance after a single Pst DC3000 challenge, it showed significantly increased resistance upon Pst DC3000 pretreatment, consistent with SAR activation. These lines also exhibited elevated ROS levels and increased PR expression levels (PR1, PR2, PR5, and GRXS13). Additionally, GhTGA12 physically interacts with GhNPR1, a key regulator of SAR. Collectively, this study identifies GhTGA12 as a critical SAR-positive regulator via ROS signaling, PR gene activation, and GhNPR1 interaction, offering new targets for enhancing disease resistance in cotton.
Keyword ：
Cotton Cotton GhTGA12 GhTGA12 Integrated genome and expression Integrated genome and expression Systemic acquired resistance Systemic acquired resistance TGA TGA
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| GB/T 7714 | Qian, Zhengyi , Cao, Shuyi , Jia, Qi et al. Integrated genome and expression of the TGA family in Gossypium hirsutum reveals GhTGA12 could positively regulate systemic acquired resistance [J]. | INDUSTRIAL CROPS AND PRODUCTS , 2025 , 236 . |
| MLA | Qian, Zhengyi et al. "Integrated genome and expression of the TGA family in Gossypium hirsutum reveals GhTGA12 could positively regulate systemic acquired resistance" . | INDUSTRIAL CROPS AND PRODUCTS 236 (2025) . |
| APA | Qian, Zhengyi , Cao, Shuyi , Jia, Qi , Zhang, Xiangyu , Du, Xinling , Su, Yina et al. Integrated genome and expression of the TGA family in Gossypium hirsutum reveals GhTGA12 could positively regulate systemic acquired resistance . | INDUSTRIAL CROPS AND PRODUCTS , 2025 , 236 . |
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芸薹属(Brassica)植物包含3个二倍体基本种及由3个基本种两两杂交和基因组加倍形成的复合种，即异源四倍体种，其进化历程一直被用作本科遗传学教学中阐述物种形成和染色体数目变异机制的经典案例。本文以芸薹属植物作为遗传学实验教学材料进行了实践探索，从形态观察到染色体观察，再到染色体倍性和核型分析，形成一个综合性实验体系，让学生从宏观到微观，深入透彻理解染色体倍性与物种形成的关系，领会多倍体形成的理论及其在育种实践中的应用。
Keyword ：
农林类专业 农林类专业 实验教学 实验教学 芸薹属植物 芸薹属植物 遗传学 遗传学
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| GB/T 7714 | 王伟 , 张冲 , 秦源 et al. 芸薹属植物在遗传学实验教学中的应用探索 [J]. | 遗传 , 2025 , 47 (07) : 0 . |
| MLA | 王伟 et al. "芸薹属植物在遗传学实验教学中的应用探索" . | 遗传 47 . 07 (2025) : 0 . |
| APA | 王伟 , 张冲 , 秦源 , 李占杰 , 贾琪 , 郑婷婷 . 芸薹属植物在遗传学实验教学中的应用探索 . | 遗传 , 2025 , 47 (07) , 0 . |
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选用2003-2022年通过福建省审定的22份菜用大豆品种，基于26个表型性状和30对SSR分子标记进行遗传多样性分析及分子指纹图谱构建。结果表明，22份菜用大豆7个质量性状存在16种变异类型，平均多样性指数为0.494,19个数量性状变异系数变幅为3.44%～50.60%，平均多样性指数为1.934，表明整体具有丰富的表型遗传多样性。30对SSR分子标记共检测到122个等位变异，等位变异数和有效等位变异数平均值分别为4.0667和2.7013，平均Nei′s基因多样性指数为0.5691，平均Shannon′s多态性信息指数为1.0479，多态信息含量变幅为0.0830～0.7319，平均为0.5262，其中Satt184引物的多态信息含量最高。22个品种间的遗传相似系数为0.3301～1.0000，平均为0.6341，其中沪选23-9与毛豆389之间的遗传相似数最大，青酥6号与闽豆1号间的遗传相似系数最小。聚类分析表明，22份菜用大豆基于表型性状和分子标记均被划分为3类，闽豆1号基于两种方法均被单独划分为一类，表明闽豆1号不管在表型性状还是遗传背景上都与其他品种差异较大，适合用作杂交亲本。综合考虑标记在染色体上分布、带型清晰度、多态等原则，筛选出9对引物Satt197、Satt442、Satt268、Satt005、Satt431、Satt334、Satt556、Sat＿112和Satt487，构建22份福建省菜用大豆审定品种分子指纹图谱，利用该引物组合可以区分除沪选23-9、毛豆389和浙鲜10号以外的19份菜用大豆品种。研究结果为福建省菜用大豆种质资源的高效利用和新品种选育提供了科学依据，有利于对已审定品种的区分与保护。
Keyword ：
分子标记 分子标记 指纹图谱 指纹图谱 菜用大豆 菜用大豆 遗传多样性 遗传多样性
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| GB/T 7714 | 李清华 , 颜墩炜 , 刘雨杭 et al. 福建菜用大豆审定品种遗传多样性分析和SSR标记指纹图谱构建 [J]. | 植物遗传资源学报 , 2025 , 26 (11) : 2145-2163 . |
| MLA | 李清华 et al. "福建菜用大豆审定品种遗传多样性分析和SSR标记指纹图谱构建" . | 植物遗传资源学报 26 . 11 (2025) : 2145-2163 . |
| APA | 李清华 , 颜墩炜 , 刘雨杭 , 陈盈妹 , 顾智炜 , 陈子琳 et al. 福建菜用大豆审定品种遗传多样性分析和SSR标记指纹图谱构建 . | 植物遗传资源学报 , 2025 , 26 (11) , 2145-2163 . |
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The normal metabolism of transient starch in leaves plays a vital role in determining photosynthesis and final crop yield. However, the molecular mechanisms linking abnormal transient starch metabolism to premature leaf senescence remain unclear. Here, we isolate a rice mutant, lses1, with leaf yellowing and premature senescence, as well as excessive accumulation of starch granules in chloroplasts. Genetic analysis revealed that this trait is controlled by a single recessive nuclear gene. Through BSA-seq preliminary gene mapping, map-based cloning, and sequencing alignment, the candidate gene was pinpointed to LOC_Os02g40860 on chromosome 2, which encodes OsCKI1, a casein kinase I family member. The identity of LSES1 was confirmed functionally: genetic complementation with the native genomic sequence rescued the wild-type phenotype, while CRISPR/Cas9 knockout of the gene in wild-type plants recapitulated the premature senescence. This confirmed that LSES1/OsCKI1 is involved in the regulation of leaf senescence. Notably, one improved knockout line, KO-2, displayed significant agronomic improvements in grain length, grain width, number of productive ears, and number of filled grains per panicle, along with a significant increase in grain yield per plant, highlighting its potential breeding value. Subcellular localization and tissue-specific expression analysis showed that LSES1 is primarily nuclear-localized and constitutively expressed.
Keyword ：
BSA-seq BSA-seq map-based cloning map-based cloning rice rice transitory starch transitory starch
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| GB/T 7714 | Chen, Fangyu , Zhang, Qishen , Wei, Xinyu et al. LSES1, Encoding a Member of the Casein Kinase 1 Family, Is Involved in the Regulation of Leaf Senescence in Rice [J]. | AGRONOMY-BASEL , 2025 , 15 (11) . |
| MLA | Chen, Fangyu et al. "LSES1, Encoding a Member of the Casein Kinase 1 Family, Is Involved in the Regulation of Leaf Senescence in Rice" . | AGRONOMY-BASEL 15 . 11 (2025) . |
| APA | Chen, Fangyu , Zhang, Qishen , Wei, Xinyu , Chen, Zhiming , Xu, Ming , Zhuang, Mancheng et al. LSES1, Encoding a Member of the Casein Kinase 1 Family, Is Involved in the Regulation of Leaf Senescence in Rice . | AGRONOMY-BASEL , 2025 , 15 (11) . |
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Food security is important for the ever-growing global population. Soybean, Glycine max (L.) Merr., is cultivated worldwide providing a key source of food, protein and oil. Hence, it is imperative to maintain or to increase its yield under different conditions including challenges caused by abiotic and biotic stresses. In recent years, the soybean pod-sucking stinkbug Riptortus pedestris has emerged as an important agricultural insect pest in East, South and Southeast Asia. Here, we present a genomics resource for R. pedestris including its genome assembly, messenger RNA (mRNA) and microRNA (miRNA) transcriptomes at different developmental stages and from different organs. As insect hormone biosynthesis genes (genes involved in metamorphosis) and their regulators such as miRNAs are potential targets for pest control, we analyzed the sesquiterpenoid (juvenile) and ecdysteroid (molting) hormone biosynthesis pathway genes including their miRNAs and relevant neuropeptides. Temporal gene expression changes of these insect hormone biosynthesis pathways were observed at different developmental stages. Similarly, a diet-specific response in gene expression was also observed in both head and salivary glands. Furthermore, we observed that microRNAs (bantam, miR-14, miR-316, and miR-263) of R. pedestris fed with different types of soybeans were differentially expressed in the salivary glands indicating a diet-specific response. Interestingly, the opposite arms of miR-281 (-5p and -3p), a miRNA involved in regulating development, were predicted to target Hmgs genes of R. pedestris and soybean, respectively. These observations among others highlight stinkbug's responses as a function of its interaction with soybean. In brief, the results of this study not only present salient findings that could be of potential use in pest management and mitigation but also provide an invaluable resource for R. pedestris as an insect model to facilitate studies on plant-pest interactions.
Keyword ：
Ecdysteroid Ecdysteroid MicroRNA MicroRNA Neuropeptide Neuropeptide Sesquiterpenoid Sesquiterpenoid Soybean Soybean Stinkbug Stinkbug Transcriptome Transcriptome
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| GB/T 7714 | Li, Chade , Nong, Wenyan , Boncan, Delbert Almerick T. et al. Elucidating the ecophysiology of soybean pod-sucking stinkbug Riptortus pedestris (Hemiptera: Alydidae) based on de novo genome assembly and transcriptome analysis [J]. | BMC GENOMICS , 2024 , 25 (1) . |
| MLA | Li, Chade et al. "Elucidating the ecophysiology of soybean pod-sucking stinkbug Riptortus pedestris (Hemiptera: Alydidae) based on de novo genome assembly and transcriptome analysis" . | BMC GENOMICS 25 . 1 (2024) . |
| APA | Li, Chade , Nong, Wenyan , Boncan, Delbert Almerick T. , So, Wai Lok , Yip, Ho Yin , Swale, Thomas et al. Elucidating the ecophysiology of soybean pod-sucking stinkbug Riptortus pedestris (Hemiptera: Alydidae) based on de novo genome assembly and transcriptome analysis . | BMC GENOMICS , 2024 , 25 (1) . |
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Drought stress is a major limit on the maize growth and productivity, and understanding the drought response mechanism is one of the important ways to improve drought resistance in maize. However, more drought-related genes and their regulated mechanisms are still to be reported. Here, we identified a novel NAC transcription factor ZmNAC55 in Zea mays and comprehensively investigated the functions of ZmNAC55 under drought stress. ZmNAC55 belonged to the NAP subfamily. ZmNAC55 had a conserved NAC domain in the N-terminal region and a divergent TAR region in the C-terminal region. ZmNAC55 was a nuclear protein, and ZmNAC55 and its TAR region had the transcriptional activation activity. Furthermore, the expression level of ZmNAC55 in leaves could be highly induced by drought stress. ZmNAC55 overexpression in Arabidopsis conferred the drought-sensitive phenotype with higher water loss, lower survival rate, higher membrane ion leakage, and higher expression levels of some drought-related genes. Meanwhile, ZmNAC55 underexpression in maize enhanced drought tolerance with lower water loss, higher survival rate, lower membrane ion leakage and lower expression levels of some drought-related genes. In addition, ZmNAC55 appeared to be very key in regulating ROS production under drought stress. Moreover, ZmNAC55 could activate ZmHOP3 expression by binding to its promoter. A novel working model of ZmNAC55 under drought stress could be found in maize. Taken together, the NAC transcription factor ZmNAC55 could negatively regulate drought stress via increasing ZmHOP3 expression in maize. ZmNAC55 is a promising candidate for improving drought resistance in maize.
Keyword ：
Drought stress Drought stress Maize Maize Molecular mechanism Molecular mechanism NAC transcription factor NAC transcription factor ZmNAC55 ZmNAC55
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| GB/T 7714 | Fan, Kai , Wu, Yuchen , Mao, Zhijun et al. A novel NAC transcription factor ZmNAC55 negatively regulates drought stress in Zea mays [J]. | PLANT PHYSIOLOGY AND BIOCHEMISTRY , 2024 , 214 . |
| MLA | Fan, Kai et al. "A novel NAC transcription factor ZmNAC55 negatively regulates drought stress in Zea mays" . | PLANT PHYSIOLOGY AND BIOCHEMISTRY 214 (2024) . |
| APA | Fan, Kai , Wu, Yuchen , Mao, Zhijun , Yin, Kan , He, Yuxi , Pan, Xinfeng et al. A novel NAC transcription factor ZmNAC55 negatively regulates drought stress in Zea mays . | PLANT PHYSIOLOGY AND BIOCHEMISTRY , 2024 , 214 . |
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Increased acid phosphatase (APase) activity is a prominent feature of tomato (Solanum lycopersicum) responses to inorganic phosphate (Pi) restriction. SlPHL1, a phosphate starvation response (PHR) transcription factor, has been identified as a positive regulator of low Pi (LP)-induced APase activity in tomato. However, the molecular mechanism underlying this regulation remains to be elucidated. Here, SlPHL1 was found to positively regulate the LP-induced expression of five potential purple acid phosphatase (PAP) genes, namely SlPAP7, SlPAP10b, SlPAP12, SlPAP15, and SlPAP17b. Furthermore, we provide evidence that SlPHL1 can stimulate transcription of these five genes by binding directly to the PHR1 binding sequence (P1BS) located on their promoters. The P1BS mutation notably weakened SlPHL1 binding to the promoters of SlPAP7, SlPAP12, and SlPAP17b but almost completely abolished SlPHL1 binding to the promoters of SlPAP10b and SlPAP15. As a result, the transcriptional activation of SlPHL1 on SlPAP10b and SlPAP15 was substantially diminished. In addition, not only did transient overexpression of either SlPAP10b or SlPAP15 in tobacco leaves increase APase activity, but overexpression of SlPAP15 in Arabidopsis and tomato also increased APase activity and promoted plant growth. Subsequently, two SPX proteins, SlSPX1 and SlSPX4, were shown to physically interact with SlPHL1. Moreover, SlSPX1 inhibited the transcriptional activation of SlPHL1 on SlPAP10b and SlPAP15 and negatively regulated the activity of APase. Taken together, these results demonstrate that SlPHL1-mediated LP signaling promotes APase activity by activating the transcription of SlPAP10b and SlPAP15, which may provide valuable insights into the mechanisms of tomato response to Pi-limited stress.
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| GB/T 7714 | Liu, Yanan , Li, Chengquan , Zhang, Duanmei et al. SlPHL1 positively modulates acid phosphatase in response to phosphate starvation by directly activating the genes SlPAP10b and SlPAP15 in tomato [J]. | PHYSIOLOGIA PLANTARUM , 2024 , 176 (1) . |
| MLA | Liu, Yanan et al. "SlPHL1 positively modulates acid phosphatase in response to phosphate starvation by directly activating the genes SlPAP10b and SlPAP15 in tomato" . | PHYSIOLOGIA PLANTARUM 176 . 1 (2024) . |
| APA | Liu, Yanan , Li, Chengquan , Zhang, Duanmei , Huang, Shaoxuan , Wang, Yi , Wang, Enhui et al. SlPHL1 positively modulates acid phosphatase in response to phosphate starvation by directly activating the genes SlPAP10b and SlPAP15 in tomato . | PHYSIOLOGIA PLANTARUM , 2024 , 176 (1) . |
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Protein phosphatase 2 C (PP2C) gene family is known for regulating a variety of abiotic stresses in plants. However, little is currently understood about this gene family in jute. In this study, a total of 60 CcPP2C genes were identified in jute, which were named from CcPP2C1 to CcPP2C60 according to the order of their physical coordinates. These CcPP2C proteins contained about 162-1324 amimo acids. Their isoelectric points varied in the range of 4.51-9.45, and their molecular weights varied from 18.307 to 146.906 kDa. The evolutionary tree of PP2Cs in jute and Arabidopsis indicated that PP2Cs can be divided into 12 branches. Sixty-seven collinear gene pairs were identified between 42 CcPP2Cs and 62 AtPP2Cs by analyzing the whole genome collinearity data of jute and Arabidopsis. The analyses of conserved motifs in these CcPP2C proteins and cis-elements in the promoters revealed that CcPP2Cs might play an extensive role in responses to various abiotic stresses in jute. Particularly, the expression patterns of CcPP2Cs in group A under salt treatments showed that CcPP2C51 was up-regulated under various stress treatments. And CcPP2C51 was localized in the nucleus and cell membrane. In Arabidopsis, the overexpression of CcPP2C51 positively regulated the salt-tolerance genes. Also, the overexpression of CcPP2C51 improved the salt tolerance of jute regenerated roots. This study revealed the origin and evolution of PP2C genes in jute, and provides potential possibilities for molecular breeding of jute.
Keyword ：
Corchorus capsularis Corchorus capsularis Expression pattern Expression pattern Gene family Gene family Protein -protein interaction Protein -protein interaction Salt stress Salt stress
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| GB/T 7714 | Pan, Xueqing , Wei, Huawei , Afzal, Muhammad Zohaib et al. Genome-wide identification of PP2C gene family and functional analysis of CcPP2C51 under salt stress in jute (Corchorus capsularis) [J]. | INDUSTRIAL CROPS AND PRODUCTS , 2024 , 214 . |
| MLA | Pan, Xueqing et al. "Genome-wide identification of PP2C gene family and functional analysis of CcPP2C51 under salt stress in jute (Corchorus capsularis)" . | INDUSTRIAL CROPS AND PRODUCTS 214 (2024) . |
| APA | Pan, Xueqing , Wei, Huawei , Afzal, Muhammad Zohaib , Gao, Shurong , Yuan, Siqi , Huang, Jinping et al. Genome-wide identification of PP2C gene family and functional analysis of CcPP2C51 under salt stress in jute (Corchorus capsularis) . | INDUSTRIAL CROPS AND PRODUCTS , 2024 , 214 . |
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