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The H2S-responsive transcription factor ERF.D3 regulates tomato abscisic acid metabolism, leaf senescence, and fruit ripening. H2S反应性转录因子ERF.D3调控番茄赤霉酸代谢、叶片衰老和果实成熟。
IF 6.5 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-21 DOI: 10.1093/plphys/kiae560
Kangdi Hu, Meihui Geng, Lin Ma, Gaifang Yao, Min Zhang, Hua Zhang

Hydrogen sulfide (H2S) is a signaling molecule that regulates plant senescence. In this study, we found that H2S delays dark-induced senescence in tomato (Solanum lycopersicum) leaves. Transcriptome and RT-qPCR analyses revealed an Ethylene Response Factor ERF.D3 is quickly induced by H2S. H2S also persulfidated ERF.D3 at amino acid residues C115 and C118. CRISPR/Cas9-mediated gene editing and gene overexpression analyses showed that ERF.D3 negatively regulates leaf senescence and fruit ripening. Abscisic acid (ABA) levels were reduced by ERF.D3 overexpression, suggesting ERF.D3 might regulate ABA metabolism. Additionally, the abscisic acid 8'-hydroxylase-encoding gene CYP707A2, which is required for ABA degradation, was identified as an ERF.D3 target gene through transcriptome data, RT-qPCR, dual-luciferase reporter assays and electrophoretic mobility shift assays. ERF.D3 persulfidation enhanced its transcriptional activity towards CYP707A2. Moreover, the E3 ligase RNF217 ubiquitinated ERF.D3, which may accelerate fruit ripening during the late stage of fruit development. Overall, our study provides valuable insights into the roles of a H2S-responsive ERF.D3 and its persulfidation state in delaying leaf senescence and fruit ripening and provides a link between H2S and ABA degradation.

硫化氢(H2S)是一种调节植物衰老的信号分子。在这项研究中,我们发现 H2S 能延缓番茄(Solanum lycopersicum)叶片在黑暗诱导下的衰老。转录组和 RT-qPCR 分析显示,乙烯反应因子 ERF.D3 被 H2S 快速诱导。H2S 还使 ERF.D3 的氨基酸残基 C115 和 C118 发生过硫化。CRISPR/Cas9 介导的基因编辑和基因过表达分析表明,ERF.D3 负向调节叶片衰老和果实成熟。ERF.D3的过表达降低了脱落酸(ABA)水平,表明ERF.D3可能调节ABA代谢。此外,通过转录组数据、RT-qPCR、双荧光素酶报告实验和电泳迁移实验,发现脱落酸 8'-羟化酶编码基因 CYP707A2 是 ERF.D3 的靶基因,该基因是 ABA 降解所必需的。ERF.D3 的过硫化作用增强了其对 CYP707A2 的转录活性。此外,E3 连接酶 RNF217 泛素化 ERF.D3,这可能会加速果实发育后期的成熟。总之,我们的研究为了解 H2S 响应性 ERF.D3 及其过硫化状态在延迟叶片衰老和果实成熟中的作用提供了宝贵的见解,并提供了 H2S 与 ABA 降解之间的联系。
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引用次数: 0
GLABRA3-mediated trichome branching requires transcriptional repression of MICROTUBULE-DESTABILIZING PROTEIN25. GLABRA3 介导的毛状体分枝需要 MICROTUBULE-DESTABILIZING PROTEIN25 的转录抑制。
IF 6.5 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-21 DOI: 10.1093/plphys/kiae563
Wenfei Xie, Yuang Zhao, Xianwang Deng, Ruixin Chen, Zhiquan Qiang, Pedro García-Caparros, Tonglin Mao, Tao Qin

Microtubules play pivotal roles in establishing trichome branching patterns, which is a model system for studying cell-shape control in Arabidopsis (Arabidopsis thaliana). However, the signaling pathway that regulates microtubule reorganization during trichome branching remains poorly understood. In this study, we report that MICROTUBULE-DESTABILIZING PROTEIN25 (MDP25) is involved in GLABRA3 (GL3)-mediated trichome branching by regulating microtubule stability. Loss of MDP25 function led to excessive trichome branching, and this phenotype in mdp25 could not be rescued by the MDP25 K7A or MDP25 K18A mutated variants. Pharmacological treatment and live-cell imaging revealed increased microtubule stability in the mdp25 mutant. Furthermore, the microtubule collar observed during trichome branching remained more intact in mdp25 compared to the WT under oryzalin treatment. Results of genetic assays further demonstrated that knocking out MDP25 rescued the reduced branching phenotype of gl3 trichomes. In gl3 trichomes, normal microtubule organization was disrupted, and microtubule stability was significantly compromised. Moreover, GL3 physically bound to the MDP25 promoter, thereby inhibiting its expression. Overexpression of GL3 negated the effects of PMDP25-driven MDP25 or its mutant proteins on trichome branching and microtubules in the mdp25 background. Overall, our study uncovers a mechanism by which GL3 inhibits MDP25 transcription, thereby influencing microtubule stability and regulating trichome branching. This mechanism provides a connection between early regulatory components and microtubules during trichome development.

微管在建立毛状体分枝模式中起着关键作用,而毛状体分枝模式是研究拟南芥(Arabidopsis thaliana)细胞形状控制的一个模型系统。然而,人们对毛状体分枝过程中调节微管重组的信号通路仍然知之甚少。在这项研究中,我们报告了微管破坏蛋白25(MDP25)通过调节微管稳定性参与了GLABRA3(GL3)介导的毛状体分枝。MDP25 功能缺失会导致毛状体分支过多,而 MDP25 K7A 或 MDP25 K18A 突变变体无法挽救 mdp25 的这种表型。药理处理和活细胞成像显示,mdp25 突变体的微管稳定性增强。此外,在毛状体分枝过程中观察到的微管轴环在奥利唑啉处理下比在 WT 中保持得更完整。基因检测结果进一步证明,敲除MDP25可以挽救gl3毛状体分支减少的表型。在gl3毛状体中,正常的微管组织被破坏,微管的稳定性受到显著影响。此外,GL3与MDP25启动子物理结合,从而抑制了其表达。在 mdp25 背景下,过量表达 GL3 可抵消 PMDP25 驱动的 MDP25 或其突变体蛋白对毛状体分枝和微管的影响。总之,我们的研究发现了GL3抑制MDP25转录从而影响微管稳定性和调控毛状体分枝的机制。这一机制提供了毛状体发育过程中早期调控成分与微管之间的联系。
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引用次数: 0
Mechanistic effects of lipid binding pockets within soluble signaling proteins: Lessons from acyl-CoA-binding and START-domain-containing proteins. 可溶性信号蛋白中脂质结合口袋的机制效应:从酰基-CoA 结合蛋白和含 START 域蛋白中汲取的教训
IF 6.5 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-21 DOI: 10.1093/plphys/kiae565
Shiu-Cheung Lung, Mee-Len Chye

While lipids serve as important energy reserves, metabolites, and cellular constituents in all forms of life, these macromolecules also function as unique carriers of information in plant communication given their diverse chemical structures. The signal transduction process involves a sophisticated interplay between messengers, receptors, signal transducers, and downstream effectors. Over the years, an array of plant signaling proteins have been identified for their crucial roles in perceiving lipid signals. However, the mechanistic effects of lipid binding on protein functions remain largely elusive. Recent literature has presented numerous fascinating models that illustrate the significance of protein-lipid interactions in mediating signaling responses. This review focuses on the category of lipophilic signaling proteins that encompass a hydrophobic binding pocket located outside of cellular membranes and provides an update on the lessons learned from two of these structures, namely the acyl-CoA-binding and START domains. It begins with a brief overview of the latest advances in understanding the functions of the two protein families in plant communication. The second part highlights five functional mechanisms of lipid ligands in concert with their target signaling proteins.

脂质在所有生命形式中都是重要的能量储备、代谢物和细胞成分,而由于其化学结构的多样性,这些大分子在植物通讯中也是独特的信息载体。信号转导过程涉及信使、受体、信号转换器和下游效应器之间复杂的相互作用。多年来,一系列植物信号蛋白因其在感知脂质信号中的关键作用而被发现。然而,脂质结合对蛋白质功能的机理影响在很大程度上仍然难以捉摸。最近的文献提出了许多引人入胜的模型,说明了蛋白质-脂质相互作用在介导信号反应中的重要作用。本综述将重点放在亲脂信号蛋白的类别上,这类蛋白包含一个位于细胞膜外的疏水结合袋,并提供了从其中两种结构(即酰基-CoA 结合结构域和 START 结构域)中吸取的最新经验教训。报告首先简要概述了在了解这两个蛋白家族在植物通讯中的功能方面取得的最新进展。第二部分重点介绍了脂质配体与其目标信号蛋白协同作用的五种功能机制。
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引用次数: 0
GLABRA3-mediated trichome branching requires transcriptional repression of MICROTUBULE-DESTABILIZING PROTEIN25. GLABRA3 介导的毛状体分枝需要 MICROTUBULE-DESTABILIZING PROTEIN25 的转录抑制。
IF 7.4 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-21 DOI: 10.1093/plphys/kiae563
Wenfei Xie,Yuang Zhao,Xianwang Deng,Ruixin Chen,Zhiquan Qiang,Pedro García-Caparros,Tonglin Mao,Tao Qin
Microtubules play pivotal roles in establishing trichome branching patterns, which is a model system for studying cell-shape control in Arabidopsis (Arabidopsis thaliana). However, the signaling pathway that regulates microtubule reorganization during trichome branching remains poorly understood. In this study, we report that MICROTUBULE-DESTABILIZING PROTEIN25 (MDP25) is involved in GLABRA3 (GL3)-mediated trichome branching by regulating microtubule stability. Loss of MDP25 function led to excessive trichome branching, and this phenotype in mdp25 could not be rescued by the MDP25 K7A or MDP25 K18A mutated variants. Pharmacological treatment and live-cell imaging revealed increased microtubule stability in the mdp25 mutant. Furthermore, the microtubule collar observed during trichome branching remained more intact in mdp25 compared to the WT under oryzalin treatment. Results of genetic assays further demonstrated that knocking out MDP25 rescued the reduced branching phenotype of gl3 trichomes. In gl3 trichomes, normal microtubule organization was disrupted, and microtubule stability was significantly compromised. Moreover, GL3 physically bound to the MDP25 promoter, thereby inhibiting its expression. Overexpression of GL3 negated the effects of PMDP25-driven MDP25 or its mutant proteins on trichome branching and microtubules in the mdp25 background. Overall, our study uncovers a mechanism by which GL3 inhibits MDP25 transcription, thereby influencing microtubule stability and regulating trichome branching. This mechanism provides a connection between early regulatory components and microtubules during trichome development.
微管在建立毛状体分枝模式中起着关键作用,而毛状体分枝模式是研究拟南芥(Arabidopsis thaliana)细胞形状控制的一个模型系统。然而,人们对毛状体分枝过程中调节微管重组的信号通路仍然知之甚少。在这项研究中,我们报告了微管破坏蛋白25(MDP25)通过调节微管稳定性参与了GLABRA3(GL3)介导的毛状体分枝。MDP25 功能缺失会导致毛状体分支过多,而 MDP25 K7A 或 MDP25 K18A 突变变体无法挽救 mdp25 的这种表型。药理处理和活细胞成像显示,mdp25 突变体的微管稳定性增强。此外,在毛状体分枝过程中观察到的微管轴环在奥利唑啉处理下比在 WT 中保持得更完整。基因检测结果进一步证明,敲除MDP25可以挽救gl3毛状体分支减少的表型。在gl3毛状体中,正常的微管组织被破坏,微管的稳定性受到显著影响。此外,GL3与MDP25启动子物理结合,从而抑制了其表达。在 mdp25 背景下,过量表达 GL3 可抵消 PMDP25 驱动的 MDP25 或其突变体蛋白对毛状体分枝和微管的影响。总之,我们的研究发现了GL3抑制MDP25转录从而影响微管稳定性和调控毛状体分枝的机制。这一机制提供了毛状体发育过程中早期调控成分与微管之间的联系。
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引用次数: 0
Transcription Factor OsMYB2 Triggers Amino Acid Transporter OsANT1 expression to Regulate Rice Growth and Salt Tolerance 转录因子 OsMYB2 触发氨基酸转运体 OsANT1 的表达以调控水稻的生长和耐盐性
IF 7.4 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-19 DOI: 10.1093/plphys/kiae559
Shengsong Nie, Weiting Huang, Chongchong He, Bowen Wu, Honglang Duan, Jingjun Ruan, Quanzhi Zhao, Zhongming Fang
Amino acid transporters play important roles in plant growth and stress tolerance; however, whether the abscisic acid signaling pathway regulates their transcription in rice (Oryza sativa) under salt stress remains unclear. In this study, we report that the transcription factor OsMYB2 (MYB transcription factor 2) of the abscisic acid signaling pathway mediates the expression of the gene encoding the amino acid transporter OsANT1 (aromatic and neutral amino acid transporter 1), which positively regulates growth and salt tolerance in rice. OsANT1 was mainly expressed in the leaf blade and panicle under normal conditions and transports leucine, phenylalanine, tyrosine and proline, positively regulating tillering and yield in rice. Nevertheless, salt stress induced the accumulation of abscisic acid and strongly increased the expression level of OsANT1 in the root, resulting in enhanced salt tolerance of rice seedlings, as evidenced by higher proline concentration and antioxidant-like enzyme activities and lower malondialdehyde and hydrogen peroxide concentrations. Moreover, we showed that OsMYB2 interacts with the promoter of OsANT1 and promotes its expression. Overexpression of OsMYB2 also improved tillering, yield, and salt tolerance in rice. In conclusion, our results suggest that the transcription factor OsMYB2 triggers OsANT1 expression and regulates growth and salt tolerance in rice, providing insights into the role of the abscisic acid signaling pathway in the regulatory mechanism of amino acid transporters in response to salt stress.
氨基酸转运体在植物生长和抗逆性中发挥着重要作用;然而,赤霉酸信号途径是否调控盐胁迫下水稻(Oryza sativa)中氨基酸转运体的转录仍不清楚。本研究报告了赤霉酸信号通路的转录因子 OsMYB2(MYB 转录因子 2)介导了氨基酸转运体 OsANT1(芳香族和中性氨基酸转运体 1)的编码基因的表达,而 OsANT1 对水稻的生长和耐盐性具有正向调节作用。正常情况下,OsANT1 主要在叶片和圆锥花序中表达,转运亮氨酸、苯丙氨酸、酪氨酸和脯氨酸,对水稻的分蘖和产量有正向调节作用。然而,盐胁迫会诱导脱落酸的积累,并强烈提高 OsANT1 在根部的表达水平,从而增强水稻幼苗的耐盐性,这表现在较高的脯氨酸浓度和抗氧化酶活性以及较低的丙二醛和过氧化氢浓度。此外,我们还发现 OsMYB2 与 OsANT1 的启动子相互作用并促进其表达。过表达 OsMYB2 还能改善水稻的分蘖、产量和耐盐性。总之,我们的研究结果表明,转录因子 OsMYB2 触发 OsANT1 的表达,并调控水稻的生长和耐盐性,为研究脱落酸信号通路在氨基酸转运体应对盐胁迫的调控机制中的作用提供了深入的见解。
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引用次数: 0
Improving rice grain shape through upstream open reading frame editing-mediated translation regulation 通过上游开放阅读框编辑介导的翻译调控改善水稻粒形
IF 7.4 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-19 DOI: 10.1093/plphys/kiae557
Qingqing Yang, Wenjie Zhu, Xu Tang, Yuechao Wu, Guanqing Liu, Dongsheng Zhao, Qiaoquan Liu, Yong Zhang, Tao Zhang
Upregulating gene expression by disturbing or destroying the upstream open reading frame of target genes is an efficient strategy for improving rice grain traits.
通过干扰或破坏目标基因的上游开放阅读框来上调基因表达,是改善水稻籽粒性状的有效策略。
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引用次数: 0
A bacterial effector cleaves RIN4 to allow the dimerization and activation of its recognizing NLR. 细菌效应物会裂解 RIN4,使其识别的 NLR 二聚化并激活。
IF 7.4 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-18 DOI: 10.1093/plphys/kiae555
Manuel González-Fuente
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引用次数: 0
Get two for the price of one: GmNF-YC4 factor mediates GmEXP7-induced root developmental changes and phosphorus starvation response in soybean. 买一送一:GmNF-YC4因子介导GmEXP7诱导的大豆根系发育变化和磷饥饿响应
IF 7.4 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-18 DOI: 10.1093/plphys/kiae554
Héctor H Torres-Martínez
{"title":"Get two for the price of one: GmNF-YC4 factor mediates GmEXP7-induced root developmental changes and phosphorus starvation response in soybean.","authors":"Héctor H Torres-Martínez","doi":"10.1093/plphys/kiae554","DOIUrl":"https://doi.org/10.1093/plphys/kiae554","url":null,"abstract":"","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"40 1","pages":""},"PeriodicalIF":7.4,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142449388","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stomatal closure as a driver of minimum leaf conductance declines at high temperature and vapor pressure deficit in Quercus. 气孔关闭是柞树在高温和蒸汽压力不足条件下叶片最小传导率下降的驱动因素。
IF 7.4 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-17 DOI: 10.1093/plphys/kiae551
J Zailaa,C Scoffoni,C R Brodersen
Rising global temperatures and vapor pressure deficits (VPD) are increasing plant water demand and becoming major drivers of large-scale plant mortality. Controlling transient leaf water loss after stomatal closure (gmin) is recognized as a key trait determining how long plants survive during soil drought. Yet, substantial uncertainty remains regarding how gmin responds to elevated temperatures and VPD and the underlying mechanisms. We measured gmin in 24 Quercus species from temperate and Mediterranean climates to determine if gmin was sensitive to a coupled temperature and VPD increase. We also explored mechanistic links to phenology, climate, evolutionary history, and leaf anatomy. We found that gmin in all species exhibited a non-linear negative temperature and VPD dependence. At 25°C (VPD = 2.2 kPa), gmin varied from 1.19 to 8.09 mmol m-2 s-1 across species but converged to 0.57 ± 0.06 mmol m-2 s-1 at 45°C (VPD = 6.6 kPa). In a subset of species, the effect of temperature and VPD on gmin was reversible and linked to the degree of stomatal closure, which was greater at 45°C than at 25°C. Our results show that gmin is dependent on temperature and VPD, is highly conserved in Quercus species, and is linked to leaf anatomy and stomatal behavior.
全球气温升高和蒸气压不足(VPD)正在增加植物的需水量,并成为植物大规模死亡的主要原因。控制气孔关闭后的瞬时叶片失水(gmin)被认为是决定植物在土壤干旱中存活多长时间的关键特征。然而,关于 gmin 对温度升高和 VPD 的反应及其内在机制,仍然存在很大的不确定性。我们测量了温带和地中海气候条件下 24 种柞树的 gmin,以确定 gmin 是否对温度和 VPD 上升的耦合效应敏感。我们还探讨了与物候、气候、进化史和叶片解剖学之间的机理联系。我们发现,所有物种的 gmin 都与温度和 VPD 呈非线性负相关。在 25°C(VPD = 2.2 kPa)时,各物种的 gmin 变化范围为 1.19 至 8.09 mmol m-2 s-1,但在 45°C(VPD = 6.6 kPa)时,gmin 趋近于 0.57 ± 0.06 mmol m-2 s-1。在一部分物种中,温度和 VPD 对 gmin 的影响是可逆的,并且与气孔关闭程度有关,45°C 时气孔关闭程度大于 25°C。我们的研究结果表明,gmin依赖于温度和VPD,在柞树物种中高度保守,并且与叶片解剖和气孔行为有关。
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引用次数: 0
Bigger meristem, higher yield? The roles of REL2 and RELK in maize meristem function and yield enhancement. 更大的分生组织,更高的产量?REL2 和 RELK 在玉米分生组织功能和增产中的作用
IF 7.4 1区 生物学 Q1 PLANT SCIENCES Pub Date : 2024-10-17 DOI: 10.1093/plphys/kiae552
Janlo M Robil,Thu M Tran
{"title":"Bigger meristem, higher yield? The roles of REL2 and RELK in maize meristem function and yield enhancement.","authors":"Janlo M Robil,Thu M Tran","doi":"10.1093/plphys/kiae552","DOIUrl":"https://doi.org/10.1093/plphys/kiae552","url":null,"abstract":"","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"11 1","pages":""},"PeriodicalIF":7.4,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142447995","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Plant Physiology
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