Plant hormones (Literature sources on phytohormones and plant signalling)
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Natural variant of Rht27, a dwarfing gene, enhances yield potential in wheat  

Authors: Xiaolin Liu, Shusong Zheng, Shuiquan Tian, Yaoqi Si, Shengwei Ma, Hong-Qing Ling and Jianqing Niu.


Theoretical and Applied Genetics (2024)


Key message: Discovery of Rht27, a dwarf gene in wheat, showed potential in enhancing grain yield by reducing plant height. 


Abstract: "Plant height plays a crucial role in crop architecture and grain yield, and semi-dwarf Reduced Height (Rht) alleles contribute to lodging resistance and were important in “Green Revolution.” However, the use of these alleles is associated with some negative side effects in some environments, such as reduced coleoptile length, low nitrogen use efficiency, and reduced yield. Therefore, novel dwarf gene resources are needed to pave an alternative route to overcome these side effects. In this study, a super-dwarf mutant rht27 was obtained by the mutagenesis of G1812 (Triticum urartu, the progenitor of the A sub-genome of common wheat). Genetic analysis revealed that the dwarf phenotype was regulated by a single recessive genetic factor. The candidate region for Rht27 was narrowed to a 1.55 Mb region on chromosome 3, within which we found two potential candidate genes that showed polymorphisms between the mutant and non-mutagenized G1812. Furthermore, the natural variants and elite haplotypes of the two candidates were investigated in a natural population of common wheat. The results showed that the natural variants affect grain yield components, and the dwarf haplotypes show the potential in improving agronomic traits and grain yield. Although the mutation in Rht27 results in severe dwarf phenotype in T. urartu, the natural variants in common wheat showed desirable phenotype, which suggests that Rht27 has the potential to improve wheat yield by utilizing its weak allelic mutation or fine-tuning its expression level."

Julio Retamales's insight:
This relevant article can be accessed by using the following link:


Text of figure above: "rht27 plants are GA sensitive and contain a low level of endogenous GA contents. The phenotype (a) and bar graphs of plant height (b) of G1812 and rht27 under the treatments of GA3 and distilled water in the green house conditions. Bar graphs of bioactive GA contents of GA1 (c), GA3 (d), GA4 (e), and GA7 (f)."
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DIV1: The Master of Awakening Seeds in Harsh Salinity Stress 

Authors: Baolei Li and Jiaqi Sun.


Plant Physiology (2024)


Excerpt: "The functions of DIVARICATA (DIV) proteins, which belong to the MYB-like TF family, remain elusive (Fang et al., 2018). Six DIV genes have been identified in Arabidopsis based on their structural resemblance to the tomato I-box binding factor SlMYBI (Machemer et al., 2011). Among these, only DIV2 has been characterized as a positive regulator of seed germination in response to ABA and salt stress (Fang et al., 2018). However, the roles of the other DIV genes in the process of seed germination in response to salinity stress remain largely unexplored. In this issue of Plant Physiology, Zhang et al. (2024) provide evidence that DIV1 functions as a crucial integrative regulator that links salinity stress with ABA/GA signaling during seed germination."


"In summary, Zhang et al. (2024) illustrate the significant role of DIV1 as a positive regulator of Arabidopsis seed germination in response to salinity stress. DIV1 exerts a direct influence on ABA/GA signaling by promoting GASA4 expression and suppressing DOGL3 expression. Additionally, it indirectly modulates the expression of a series of germination-associated genes.

Julio Retamales's insight:
Commentary on the relevant article by Zhang et al. ("Transcription factor DIVARICATA1 positively modulates seed germination in response to salinity stress"), which is posted here.

Text of figure above: "Figure 1. Simplified Model of DIV1-Mediated Regulation of Seed Germination. This model illustrates how DIV1 expression is induced by gibberellic acid (GA) and repressed by salinity, osmotic stress, and abscisic acid (ABA). NF-YC9 directly inhibits DIV1 expression. In turn, DIV1 directly influences the expression of DOGL3 and GASA4 and indirectly affects a range of other genes associated with germination in response to salinity stress. Arrows and T-bars represent promoting and inhibitory effects, respectively. Solid lines indicate direct transcriptional regulation, while dotted lines denote indirect transcriptional regulation."
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The apple MdGA2ox7 modulates the balance between growth and stress tolerance in an anthocyanin-dependent manner

Authors: Rui Yan, Tianle Zhang, Yuan Wang, Wenxiu Wang, Rahat Sharif, Jiale Liu, Qinglong Dong, Haoan Luan, Xuemei Zhang, Han Li, Suping Guo, Guohui Qi and Peng Jia. 

Plant Physiology and Biochemistry (2024)

Highlights: • Seventeen GA2-oxidase genes identified in apple clustered into four clades. • MdGA2ox7 responded to cold and salt treatments. • MdGA2ox7 was activated during light-induced anthocyanin accumulation. • MdGA2ox7 alleviated cold and salt stress damage. • MdGA2ox7 promoted anthocyanin biosynthesis.

Abstract: "Apple (Malus domestica Borkh.) is a widely cultivated fruit crop worldwide but often suffers from abiotic stresses such as salt and cold. Gibberellic acid (GA) plays a pivotal in controlling plant development, environmental adaptability, and secondary metabolism. The GA2-oxidase (GA2ox) is responsible for the deactivation of bioactive GA. In this study, seventeen GA2-oxidase genes were identified in the apple genome, and these members could be clustered into four clades based on phylogenetic relationships and conserved domain structures. MdGA2ox7 exhibited robust expression across various tissues, responded to cold and salt treatments, and was triggered in apple fruit peels via light-induced anthocyanin accumulation. Subcellular localization prediction and experiments confirmed that MdGA2ox7 was located in the cytoplasm. Overexpression of MdGA2ox7 in Arabidopsis caused a lower level of active GA and led to GA-deficient phenotypes, such as dwarfism and delayed flowering. MdGA2ox7 alleviated cold and salt stress damage in both Arabidopsis and apple in concert with melatonin (MT). Additionally, MdGA2ox7 enhanced anthocyanin biosynthesis in apple calli and activated genes involved in anthocyanin synthesis. These findings provide new insights into the functions of apple GA2ox in regulating development, stress tolerance, and secondary metabolism."

Julio Retamales's insight:
Text of figure above: "Fig. 3. The expression pattern of MdGA2ox7 and the alleviative effect of MT on the injury of apples to cold and salt stress. (A) GUS staining showed the promoter activity of MdGA2ox7 in different Arabidopsis tissues. (B) GUS staining and activity measurement showed the response of MdGA2ox7 promoter activity to cold and salt stress. (C) Phenotypic comparison of apple seedlings with and without MT supplementation under cold and salt stress. (D) – (E) Detection of reactive oxygen species (ROS) under different stress conditions. (D) Nitro Blue Tetrazolium (NBT) staining showed the accumulation of superoxide anion radical in apple leaves under different stress and MT applications. (E) The content of superoxide anion radical in apple leaves. Bar = 1 cm."
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DELLA proteins recruit the Mediator complex subunit MED15 to coactivate transcription in land plants

DELLA proteins recruit the Mediator complex subunit MED15 to coactivate transcription in land plants | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it
Authors: Jorge Hernández-García, Antonio Serrano-Mislata, María Lozano-Quiles, Cristina Úrbez, María A. Nohales, Noel Blanco-Touriñán, Huadong Peng, Rodrigo Ledesma-Amaro and Miguel A. Blázquez. 

PNAS (2024)

Significance: DELLA proteins are plant-specific transcriptional hubs integrating environmental signals with endogenous cues. In order to regulate downstream processes, DELLAs modulate the activity of hundreds of transcription factors (TFs) and transcriptional regulators in various ways. Here, we describe the molecular mechanism underlying DELLA coactivator function. We show that DELLAs act as transcriptional activators by interacting with the Mediator complex subunit MED15. This interaction is necessary to regulate a specific subset of DELLA-dependent responses that are mediated by transcriptional coactivation, but not those regulated by TF sequestration. We further show that this mechanism is present in bryophyte DELLAs and thus represents a conserved mechanism of DELLA function in land plants.

Abstract: "DELLA proteins are negative regulators of the gibberellin response pathway in angiosperms, acting as central hubs that interact with hundreds of transcription factors (TFs) and regulators to modulate their activities. While the mechanism of TF sequestration by DELLAs to prevent DNA binding to downstream targets has been extensively documented, the mechanism that allows them to act as coactivators remains to be understood. Here, we demonstrate that DELLAs directly recruit the Mediator complex to specific loci in Arabidopsis, facilitating transcription. This recruitment involves DELLA amino-terminal domain and the conserved MED15 KIX domain. Accordingly, partial loss of MED15 function mainly disrupted processes known to rely on DELLA coactivation capacity, including cytokinin-dependent regulation of meristem function and skotomorphogenic response, gibberellin metabolism feedback, and flavonol production. We have also found that the single DELLA protein in the liverwort Marchantia polymorpha is capable of recruiting MpMED15 subunits, contributing to transcriptional coactivation. The conservation of Mediator-dependent transcriptional coactivation by DELLA between Arabidopsis and Marchantia implies that this mechanism is intrinsic to the emergence of DELLA in the last common ancestor of land plants."
Julio Retamales's insight:
Major contribution!

This relevant paper was already posted here when published as a preprint.
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Sub1 QTL confers submergence tolerance in rice through nitro-oxidative regulation and phytohormonal signaling

Authors: Sahana Basu, Monika, Surbhi Kumari and Gautam Kumar. 

Plant Physiology and Biochemistry (2024)

Highlights: • IAA induces lateral root formation in rice under submergence • ROS and RNS cause lysigenous aerenchyma formation in root cortex of rice • Submergence decreases ABA level, causing GA-mediated escape response in rice shoot • Enhanced antioxidant levels dampen nitro-oxidative damage during de-submergence 

Abstract: "Constant change in global climate has become the most important limiting factor to crop productivity. Asymmetrical precipitations are causing recurrent flood events around the world. Submergence is one of the most detrimental abiotic stresses for sustainable rice production in the rainfed ecosystems of Southeast Asia. Therefore, the development of submergence-tolerant rice is an essential requirement to encounter food security. Submergence tolerance in rice is governed by the major quantitative trait locus (QTL) designated as Submergence1 (Sub1) near the centromere of chromosome 9. The introduction of the Sub1 in high-yielding rice varieties producing near-isogenic lines (NILs) has shown extreme submergence tolerance. The present study aimed to understand the responses of rice genotype IR64 and its Sub1 NIL IR64 Sub1 following one week of complete submergence treatment. Submergence imposed severe nitro-oxidative stress in both the rice genotypes, consequently disrupting the cellular redox homeostasis. In this study, IR64 exhibited higher NADPH oxidase activity accompanied by increased reactive oxygen species, reactive nitrogen species, and malondialdehyde buildups and cell death under submergence. Higher accumulations of 1-Aminocyclopropane-1-carboxylic acid, gibberellic acid, and Indole-3-acetic acid were also observed in IR64 which accelerated the plant growth and root cortical aerenchyma development following submergence. In contrast, IR64 Sub1 had enhanced submergence tolerance associated with an improved antioxidant defense system with sustainable morpho-physiological activities and restricted root aerenchyma formation. The comprehensive analyses of the responses of rice genotypes with contrasting submergence tolerance may demonstrate the intricacies of rice under complete submergence and may potentially contribute to improving stress resilience by advancing our understanding of the mechanisms of submergence tolerance in rice."
Julio Retamales's insight:
Text of figure above: "Fig. 7. Illustration of Sub1A-mediated phytohormone and ROS/RNS regulation associated with submergence acclimation. Submergence stimulates the synthesis of the gaseous phytohormone ethylene in the submerged plant cells. Submergence tolerance in rice is facilitated by Sub1A, which is an ethylene-responsive factor. Submergence-induced ethylene accumulation activates the Sub1A, which in turn prevents ethylene production through feedback inhibition. Alternatively, Sub1A activates IAA synthesis, thereby inducing lysigenous root cortical aerenchyma and lateral root formation. Sub1A also limits GA synthesis and responses resulting in suppression of root/shoot elongation with restricted carbohydrate consumption. Additionally, Sub1A stimulates the antioxidant defense system contributing to ROS and RNS scavenging, consequently conferring submergence tolerance in rice."
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PsmiR159b-PsMYB65 module functions in the resumption of bud growth after endodormancy by affecting the cell cycle in tree peony 

Authors: Tao Zhang, Xinyu Wang, Yanchao Yuan, Shoujie Zhu, Chunying Liu, Yuxi Zhang, Shupeng Gai.


Horticulture Research (2024)


Abstract: "Bud endodormancy in perennial plants is a sophisticated system that adapts to seasonal climatic changes. Growth-promoting signals such as low temperature and gibberellins (GAs) are crucial for facilitating budbreak following endodormancy release (EDR). However, the regulatory mechanisms underlying GA-mediated budbreak in tree peony (Paeonia suffruticosa) remain unclear. In tree peony, the expression of PsmiR159b among three differentially expressed miR159 members was inhibited with the prolonged chilling, and overexpression of PsMIR159b delayed budbreak, whereas silencing PsmiR159b promoted budbreak after dormancy. PsMYB65, a downstream transcription factor in the GA pathway, was induced by prolonged chilling and exogenous GA3 treatments. PsMYB65 was identified as a target of PsmiR159b, and promoted budbreak in tree peony. RNA-seq of PsMYB65-silenced buds revealed significant enrichment in the GO terms regulation of ‘cell cycle’ and ‘DNA replication’ among differentially expressed genes. Yeast one-hybrid and electrophoretic mobility shift assays demonstrated that PsMYB65 directly bound to the promoter of the type-D cyclin gene PsCYCD3;1. Dual-luciferase reporter assay indicated that PsMYB65 positively regulate PsCYCD3;1 expression, suggesting that miR159b-PsMYB65 module contributes to budbreak by influencing the cell cycle. Our findings revealed that the PsmiR159b-PsMYB65 module functioned in budbreak after dormancy by regulating cell proliferation, providing valuable insights into the endodormancy release regulation mechanism."

Julio Retamales's insight:
Text of figure above: "PsmiR159b inhibited tree peony budbreak. (A) Morphology of PsMIR159b-overexpressing (OE-MIR159b) and PsMIR159b-silenced (STTM159b) buds. pCVA, transgenic buds with empty pCVA vector. Buds were pictured at 10 and 20 d after infection (DAI). Scale bar, 5 mm. (B) Relative level of PsmiR159b at 10 DAI. (C) Relative growth rate of OE-MIR159b and STTM159b buds at 10 and 20 DAI. (D) Expression levels of D-type cyclin (CYCDs) in OE-MIR159b, STTM159b buds and control at 10 DAI." 
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Molecular Advances of Bud Dormancy in Trees - Review 

Molecular Advances of Bud Dormancy in Trees - Review  | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it

Authors: Jihua Ding, Kejing Wang, Shashank Pandey, Mariano Perales, Isabel Allona, Md Rezaul Islam Khan, Victor B. Busov, Rishikesh P. Bhalerao


Journal of Experimental Botany (2024)


Abstract: "Seasonal bud dormancy in perennial woody plants is a crucial and intricate process that is vital for the survival and development of plants. Over the past few decades, significant advancements have been made in understanding many features of bud dormancy, particularly in model species, where certain molecular mechanisms underlying this process have been elucidated. In this review, we provide an overview of recent molecular progress in understanding bud dormancy in trees, with a specific emphasis on the integration of common signaling and molecular mechanisms identified across different tree species. Additionally, we address some challenges that have emerged in the in-depth understanding of bud dormancy and offer insights for future studies."

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Plant Quiescence Strategy and Seed Dormancy under Hypoxia - Review    

Plant Quiescence Strategy and Seed Dormancy under Hypoxia - Review     | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it

Authors: Chiara Pucciariello and Pierdomenico Perata.


Journal of Experimental Botany (2024)


Abstract: "Plant quiescence and seed dormancy can be triggered by reduced oxygen availability. Under water, oxygen depletion caused by flooding can culminate in a quiescent state, which is a plant strategy for energy preservation and survival. In adult plants, a quiescent state can be activated by sugar starvation, culminating in metabolic depression. In seeds, secondary dormancy can be activated by reduced oxygen availability, which creates an unfavourable state for germination. The physical dormancy of some seeds and buds includes barriers to external conditions, which indirectly results in hypoxia. The molecular processes that support seed dormancy and plant survival through quiescence under hypoxia include the N-degron pathway, which enables the modulation of ethylene responsive factors of group VII and downstream targets. This oxygen- and nitric oxide-dependent mechanism interacts with phytohormone-related pathways to control growth."

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Good review!
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The homomorphic self-incompatibility system in Oleaceae is controlled by a hemizygous genomic region expressing a gibberellin pathway gene

Authors: Vincent Castric, Rita A. Batista, Amélie Carré, Soraya Mousavi, Clément Mazoyer, Cécile Godé, Sophie Gallina, Chloé Ponitzki, Anthony Theron, Arnaud Bellec, William Marande, Sylvain Santoni, Roberto Mariotti, Andrea Rubini, Sylvain Legrand, Sylvain Billiard, Xavier Vekemans, Philippe Vernet and Pierre Saumitou-Laprade.

Current Biology (2024)

Editor's view: The self-incompatibility system of the Oleaceae is unusual, with the long-term maintenance of only two groups of reproductive compatibility. Castric et al. identify a hemizygous chromosomal fragment unique to one specificity, containing a single conserved gene with predicted function in catabolism of gibberellin.

Highlights: • The segregation of a genome fragment controls self-incompatibility (SI) in Oleaceae • This is the first report of hemizygous control of a homomorphic SI system • This fragment contains a single conserved gene, related to the gibberellin pathway • Manipulation of gibberellin levels switches self-incompatibility specificities 

Abstract; "In flowering plants, outcrossing is commonly ensured by self-incompatibility (SI) systems. These can be homomorphic (typically with many different allelic specificities) or can accompany flower heteromorphism (mostly with just two specificities and corresponding floral types). The SI system of the Oleaceae family is unusual, with the long-term maintenance of only two specificities but often without flower morphology differences. To elucidate the genomic architecture and molecular basis of this SI system, we obtained chromosome-scale genome assemblies of Phillyrea angustifolia individuals and related them to a genetic map. The S-locus region proved to have a segregating 543-kb indel unique to one specificity, suggesting a hemizygous region, as observed in all distylous systems so far studied at the genomic level. Only one of the predicted genes in this indel region is found in the olive tree, Olea europaea, genome, also within a segregating indel. We describe complete association between the presence/absence of this gene and the SI types determined for individuals of seven distantly related Oleaceae species. This gene is predicted to be involved in catabolism of the gibberellic acid (GA) hormone, and experimental manipulation of GA levels in developing buds modified the male and female SI responses of the two specificities in different ways. Our results provide a unique example of a homomorphic SI system, where a single conserved gibberellin-related gene in a hemizygous indel underlies the long-term maintenance of two groups of reproductive compatibility."
Julio Retamales's insight:
This relevant article should be considered together with the one by Raimondeau et al. (" A hemizygous supergene controls homomorphic and heteromorphic self-incompatibility systems in Oleaceae"), also posted here.

Text of figure above: "Figure 5. Treatment with gibberellin modifies the male and female SI responses of the two specificities in different manners (A) Fluorescent microscopic images of controlled pollination assays in Ligustrum vulgare. Compatible and incompatible reactions (indicated in the bottom right corner of each image) are identified based on the presence of germinated pollen tubes reaching the style. (B) Graphical summary of the effect of the GA supplementation assay, illustrating that pistils of the [Ha] specificity and pollen of the [Hb] specificity were GA insensitive, while, conversely, pollen of the [Ha] specificity and pistils of the [Hb] specificity switched specificity upon GA3 treatment."
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C-TERMINAL DOMAIN PHOSPHATASE-LIKE 3 contributes to GA-mediated growth and flowering by interaction with DELLA proteins

Authors: Ting Li, Yongqin Wang, Annelore Natran, Yi Zhang, Hao Wang, Kangxi Du, Peng Qin, Hua Yuan, Weilan Chen, Bin Tu, Dirk Inzé and Marieke Dubois. 

New Phytologist (2024)

Abstract: "Gibberellic acid (GA) plays a central role in many plant developmental processes and is crucial for crop improvement. DELLA proteins, the core suppressors in the GA signaling pathway, are degraded by GA via the 26S proteasomal pathway to release the GA response. However, little is known about the phosphorylation-mediated regulation of DELLA proteins. In this study, we combined GA response assays with protein–protein interaction analysis to infer the connection between Arabidopsis thaliana DELLAs and the C-TERMINAL DOMAIN PHOSPHATASE-LIKE 3 (CPL3), a phosphatase involved in the dephosphorylation of RNA polymerase II. We show that CPL3 directly interacts with DELLA proteins and promotes DELLA protein stability by inhibiting its degradation by the 26S proteasome. Consequently, CPL3 negatively modulates multiple GA-mediated processes of plant development, including hypocotyl elongation, flowering time, and anthocyanin accumulation. Taken together, our findings demonstrate that CPL3 serves as a novel regulator that could improve DELLA stability and thereby participate in GA signaling transduction."
Julio Retamales's insight:
Text of figure above: "Model showing the modulation of DELLA proteins by C-TERMINAL DOMAIN PHOSPHATASE-LIKE 3 (CPL3) in Arabidopsis. DELLAs are the core suppressors of the gibberellic acid (GA) signaling pathway and the GA-activated GA-INSENSITIVE DWARF1 (GID1) receptor targets DELLA to the ubiquitin-26S proteasome system for degradation. CPL3 likely dephosphorylates DELLA proteins via direct interaction and also stabilizes DELLA proteins by inhibiting their decay via the 26S proteasome. Given that GA promotes plant growth via the degradation of DELLA proteins, CPL3 could participate in the GA signaling transduction and regulate GA-mediated plant growth."
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Bifunctional transcription factors SlERF.H5 and H7 activate cell wall and repress gibberellin biosynthesis genes in tomato via a conserved motif

Bifunctional transcription factors SlERF.H5 and H7 activate cell wall and repress gibberellin biosynthesis genes in tomato via a conserved motif | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it
Authors: Yangang Pei, Qihan Xue, Peng Shu, Weijie Xu, Xiaofei Du, Mengbo Wu, Kaidong Liu, Julien Pirrello, Mondher Bouzayen, Yiguo Hong and Mingchun Liu. 

Developmental Cell (2024)

Editor's view: Pei et al. demonstrate the role of bifunctional transcription factors SlERF.H5 and SlERF.H7 in activating the cellulose biosynthesis gene SlCESA3 while repressing the gibberellin biosynthesis gene GA20ox1. The study highlights the distinct transcriptional regulatory functions of these ERFs in promoting cell wall formation and inhibiting plant growth.

Highlights • Cellulose is required for cell wall formation and firmness maintenance of fruits • SlERF.H5 and SlERF.H7 act as both transcriptional activators and repressors • The regulatory activity of SlERF.H5 and SlERF.H7 is mediated by a conserved motif 

Abstract: "The plant cell wall is a dynamic structure that plays an essential role in development, but the mechanism regulating cell wall formation remains poorly understood. We demonstrate that two transcription factors, SlERF.H5 and SlERF.H7, control cell wall formation and tomato fruit firmness in an additive manner. Knockout of SlERF.H5, SlERF.H7, or both genes decreased cell wall thickness, firmness, and cellulose contents in fruits during early development, especially in double-knockout lines. Overexpressing either gene resulted in thicker cell walls and greater fruit firmness with elevated cellulose levels in fruits but severely dwarf plants with lower gibberellin contents. We further identified that SlERF.H5 and SlERF.H7 activate the cellulose biosynthesis gene SlCESA3 but repress the gibberellin biosynthesis gene GA20ox1. Moreover, we identified a conserved LPL motif in these ERFs responsible for their activities as transcriptional activators and repressors, providing insight into how bifunctional transcription factors modulate distinct developmental processes."
Julio Retamales's insight:
Relevant findings!
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Advances in the molecular regulation of seed germination in plants - Review

Advances in the molecular regulation of seed germination in plants - Review | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it


Authors: Jia Zhao, Yongqi He, Hongsheng Zhang and Zhoufei Wang.


Seed Biology (2024)


Abstract: "Seed germination is a key process in the life cycle of seed plants. The initiation of seed germination requires the activity of specific internal signaling molecules, such as hormones and reactive oxygen species (ROS), and is dependent on external environmental factors, such as water, temperature, and light. Seed germination is a complex trait that is regulated by multiple factors, including transcript, protein, and metabolite levels. This review highlights current knowledge relating to the regulatory roles of hormones, ROS, small RNAs, epigenetic modifications, post-translational modifications, and environmental cues on seed germination, mainly focusing on Arabidopsis and rice. The review on the molecular regulation of seed germination contributes to the improvement of crop seed quality using bio-breeding approaches."


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Ratiometric gibberellin biosensors for the analysis of signaling dynamics and metabolism in plant protoplasts

Authors: Jennifer Andres, Lisa J. Schmunk, Federico Grau-Enguix, Justine Braguy, Sophia L. Samodelov, Tim Blomeier, Rocio Ochoa-Fernandez, Wilfried Weber, Salim Al-Babili, David Alabadí, Miguel A. Blázquez and Matias D. Zurbriggen. 

The Plant Journal (2024)

Significance Statement: Using the degradation-based signaling mechanism of GAs, we have built transcriptional regulator (DELLA)-based, genetically encoded ratiometric biosensors as proxies for hormone quantification at high temporal resolution and sensitivity that allow dynamic, rapid and simple analysis in a plant cell system, i.e. Arabidopsis protoplasts.

Abstract: "Gibberellins (GAs) are major regulators of developmental and growth processes in plants. Using the degradation-based signaling mechanism of GAs, we have built transcriptional regulator (DELLA)-based, genetically encoded ratiometric biosensors as proxies for hormone quantification at high temporal resolution and sensitivity that allow dynamic, rapid and simple analysis in a plant cell system, i.e. Arabidopsis protoplasts. These ratiometric biosensors incorporate a DELLA protein as a degradation target fused to a firefly luciferase connected via a 2A peptide to a renilla luciferase as a co-expressed normalization element. We have implemented these biosensors for all five Arabidopsis DELLA proteins, GA-INSENSITIVE, GAI; REPRESSOR-of-ga1-3, RGA; RGA-like1, RGL1; RGL2 and RGL3, by applying a modular design. The sensors are highly sensitive (in the low pm range), specific and dynamic. As a proof of concept, we have tested the applicability in three domains: the study of substrate specificity and activity of putative GA-oxidases, the characterization of GA transporters, and the use as a discrimination platform coupled to a GA agonists' chemical screening. This work demonstrates the development of a genetically encoded quantitative biosensor complementary to existing tools that allow the visualization of GA in planta."
Julio Retamales's insight:
Great tool!

Text of the figure above: "Biosynthesis and deactivation of bioactive gibberellins (GAs) in planta, GA perception mechanism in Arabidopsis thaliana and GA biosensor design. (a) The bioactive gibberellins GA1, GA3, GA4 and GA7 are synthesized from their precursors, GA20 or GA9, in a single-step or multi-step conversions mediated by GA 3-oxidases. GA 2-oxidases catalyze the catabolic deactivation of GA1 and GA4. (b) Schematic overview of the GA perception mechanism in A. thaliana. Upon binding of GAs to the co-receptor GID1, DELLAs associate with the SLY1 and SKP1/CUL1/F-box E3-ubiquitin ligase complex (SCFSLY1) and become polyubiquitylated (U), and targeted for degradation by the 26S proteasome. As a consequence, DELLA-bound transcription factors (TFs) are released and are able to bind to specific promoter regions thereby regulating gene expression (only the sequestration mechanism is shown for simplicity). goi, gene of interest. (c) The five GA biosensor constructs contain one of each DELLA as a sensor module (SM) fused to a firefly luciferase (FF). A 2A peptide connects a renilla luciferase (REN) as a normalization element with the DELLA-FF fusion which leads to stoichiometric co-expression of both polypeptides. As a consequence of GA induction, DELLA-FF becomes ubiquitylated and consequently degraded, whereas REN levels remain constant, which leads to a decrease in FF/REN ratio."
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Spark to blaze the role of ethylene in achenes and the ripple influences on strawberry fruit growth and ripening - Perspective


Authors: Huixin Chen, Dongdong Li and Kunsong Chen.


Fruit Research (2024)


Abstract: "Strawberry, considered to be a model for non-climacteric fruits, has traditionally been viewed as having a less pronounced reliance on ethylene in fruit development. However, the inherent tissue heterogeneity within strawberry fruit, coupled with variable ethylene production levels, suggests a potential role for ethylene in the maturation of the true fruit, the achenes, dispersed on the fleshy receptacle. This intricate process is likely to exert ripple effects on the subsequent growth and ripening of the receptacle. To comprehensively unravel the functions of ethylene in strawberry fruit, there is a need for ethylene detection sensors, ethylene response reporter transgenic plants, and genetically engineered mutants achieved through genome editing, encompassing both biosynthesis and signaling mutants."


Julio Retamales's insight:
Text of figure above (letter f): "(f) A diagram showing hypothesized roles of ethylene in strawberry. Ethylene is largely synthesized in the achene by ACC synthase (ACS) and ACC oxidase (ACO). Ethylene may regulate the development and maturation of achene directly and/or indirectly via actions on auxin and gibberellic acid (GA). The ethylene emitted from the achene may diffuse to the receptacle to regulate the growth and ripening of the receptacle. In addition, ACC, the ethylene biosynthesis precursor, might be transported to the receptacle from achenes via the vascular bundles. Red dashed arrows indicate hypothesized roles of ethylene in strawberry fruit."
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Transcription factor DIVARICATA1 positively modulates seed germination in response to salinity stress 

Transcription factor DIVARICATA1 positively modulates seed germination in response to salinity stress  | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it

Authors: Da Zhang, Tan He, Xumin Wang, Chenchen Zhou, Youpeng Chen, Xin Wang, Shixiang Wang, Shuangcheng He, Yuan Guo, Zijin Liu and Mingxun Chen.


Plant Physiology (2024)


One-sentence summary: A MYB-like transcription factor positively modulates seed germination in response to salinity stress by regulating the expression of germination-associated genes.


Abstract: "Seed germination is a critical checkpoint for plant growth under unfavorable environmental conditions. In Arabidopsis (Arabidopsis thaliana), the abscisic acid (ABA) and gibberellic acid (GA) signaling pathways play important roles in modulating seed germination. However, the molecular links between salinity stress and ABA/GA signaling are not well understood. Herein, we showed that the expression of DIVARICATA1 (DIV1), which encodes a MYB-like transcription factor, was induced by GA and repressed by ABA, salinity, and osmotic stress in germinating seeds. DIV1 positively regulated seed germination in response to salinity stress by directly regulating the expression of DELAY OF GERMINATION 1-LIKE 3 (DOGL3) and GA-STIMULATED ARABIDOPSIS 4 (GASA4) and indirectly regulating the expression of several germination-associated genes. Moreover, NUCLEAR FACTOR-YC9 (NF-YC9) directly repressed the expression of DIV1 in germinating seeds in response to salinity stress. These results help reveal the function of the NF-YC9–DIV1 module and provide insights into the regulation of ABA and GA signaling in response to salinity stress during seed germination in Arabidopsis."

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Stacked mutations in wheat homologues of rice SEMI-DWARF1 confer a novel semi-dwarf phenotype 

Stacked mutations in wheat homologues of rice SEMI-DWARF1 confer a novel semi-dwarf phenotype  | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it

Authors: Barbora Ndreca, Alison Huttly, Sajida Bibi, Carlos Bayon, George Lund, Joshua Ham, Rocío Alarcón-Reverte, John Addy, Danuše Tarkowská, Stephen Pearce, Peter Hedden, Stephen G. Thomas and Andrew L. Phillips.


BMC Plant Biology (2024)


Abstract: Background - Semi-dwarfing alleles are used widely in cereals to confer improved lodging resistance and assimilate partitioning. The most widely deployed semi-dwarfing alleles in rice and barley encode the gibberellin (GA)-biosynthetic enzyme GA 20-OXIDASE2 (GA20OX2). The hexaploid wheat genome carries three homoeologous copies of GA20OX2, and because of functional redundancy, loss-of-function alleles of a single homoeologue would not be selected in wheat breeding programmes. Instead, approximately 70% of wheat cultivars carry gain-of-function mutations in REDUCED HEIGHT 1 (RHT1) genes that encode negative growth regulators and are degraded in response to GA. Semi-dwarf Rht-B1b or Rht-D1b alleles encode proteins that are insensitive to GA-mediated degradation. However, because RHT1 is expressed ubiquitously these alleles have pleiotropic effects that confer undesirable traits in some environments. Results - We have applied reverse genetics to combine loss-of-function alleles in all three homoeologues of wheat GA20OX2 and its paralogue GA20OX1 and evaluated their performance in three years of field trials. ga20ox1 mutants exhibited a mild height reduction (approximately 3%) suggesting GA20OX1 plays a minor role in stem elongation in wheat. ga20ox2 mutants have reduced GA1 content and are 12–32% shorter than their wild-type segregants, comparable to the effect of the Rht-D1b ‘Green Revolution’ allele. The ga20ox2 mutants showed no significant negative effects on yield components in the spring wheat variety ‘Cadenza’. Conclusions - Our study demonstrates that chemical mutagenesis can expand genetic variation in polyploid crops to uncover novel alleles despite the difficulty in identifying appropriate mutations for some target genes and the negative effects of background mutations. Field experiments demonstrate that mutations in GA20OX2 reduce height in wheat, but it will be necessary to evaluate the effect of these alleles in different genetic backgrounds and environments to determine their value in wheat breeding as alternative semi-dwarfing alleles.

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A quantitative gibberellin signaling biosensor reveals a role for gibberellins in internode specification at the shoot apical meristem  

A quantitative gibberellin signaling biosensor reveals a role for gibberellins in internode specification at the shoot apical meristem   | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it

Authors: Bihai Shi, Amelia Felipo-Benavent, Guillaume Cerutti, Carlos Galvan-Ampudia, Lucas Jilli, Geraldine Brunoud, Jérome Mutterer, Elody Vallet, Lali Sakvarelidze-Achard, Jean-Michel Davière, Alejandro Navarro-Galiano, Ankit Walia, Shani Lazary, Jonathan Legrand, Roy Weinstain, Alexander M. Jones, Salomé Prat, Patrick Achard and Teva Vernoux.


Nature Communications (2024)


Editor's view: Engineering of a biosensor allows the authors to map the signaling activity of the phytohormones gibberellins (GAs) and to show that GAs orient cell division at the shoot apex to establish the organization in parallel cell files of plant stems.


Abstract: "Growth at the shoot apical meristem (SAM) is essential for shoot architecture construction. The phytohormones gibberellins (GA) play a pivotal role in coordinating plant growth, but their role in the SAM remains mostly unknown. Here, we developed a ratiometric GA signaling biosensor by engineering one of the DELLA proteins, to suppress its master regulatory function in GA transcriptional responses while preserving its degradation upon GA sensing. We demonstrate that this degradation-based biosensor accurately reports on cellular changes in GA levels and perception during development. We used this biosensor to map GA signaling activity in the SAM. We show that high GA signaling is found primarily in cells located between organ primordia that are the precursors of internodes. By gain- and loss-of-function approaches, we further demonstrate that GAs regulate cell division plane orientation to establish the typical cellular organization of internodes, thus contributing to internode specification in the SAM."

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Inhibition of flowering by gibberellins in the woody plant Jatropha curcas is restored by overexpression of JcFT

Authors: Ping Huang, Jie Yang, Jiapeng Ke, Li Cai, Yingxiong Hu, Jun Ni, Chaoqiong Li, Zeng-Fu Xu and Mingyong Tang. 

Plant Science (2024)

Highlights • GA4+7 and GA synthase gene JcGA20ox1 suppressed flowering in Jatropha, whereas the GA biosynthesis inhibitor paclobutrazol and GA degradation gene JcGA2ox6 promoted flowering. • JcGA20ox1 decreased the expression of JcFT; while, the inhibition of floral transition by JcGA20ox1 could restored by JcFT, and the seed yield suppression phenotype could partially restored by JcFT. • JcGA20ox1 also decreased JiFT expression and delayed floral transition in J. curcas × J. integerrima hybrids. 

Abstract: "Jatropha curcas is a perennial oil-seed plant with vigorous vegetative growth but relatively poor reproductive growth and low seed yield. Gibberellins (GA) promote flowering in most annual plants, but inhibit flower initiation in many woody plants, including J. curcas. However, the underlying mechanisms of GA inhibition on flowering in perennial woody plants remain unclear. Here, we found that overexpression of the gibberellin biosynthesis gene JcGA20ox1 delays flowering in J. curcas and in the J. curcas × J. integerrima hybrids. Consistent with this finding, overexpression of the GA catabolic gene JcGA2ox6 induces early flowering in J. curcas. qRTsingle bondPCR revealed that the inhibition of floral transition by overexpressing JcGA20ox1 resulted from the decreased of JcFT and other flowering related genes, which was restored by overexpressing JcFT in J. curcas. Overexpression of JcGA20ox1 or JcGA2ox6 reduced seed yield, but overexpression of JcFT significantly increased seed yield. Furthermore, hybridization experiments showed that the reduction in seed yield caused by overexpression of JcGA20ox1 or JcGA2ox6 was partially restored by the overexpression of JcFT. In addition, JcGA20ox1, JcGA2ox6 and JcFT were also found to be involved in the regulation of seed oil content and endosperm development. In conclusion, our study revealed the inhibitory effect of GA on flowering in J. curcas is mediated through JcFT and demonstrated the effects of JcGA20ox1, JcGA2ox6 and JcFT on agronomic traits. This study also indicates the potential value of GA metabolism genes and JcFT in breeding new varieties of woody oil-seed plants."
Julio Retamales's insight:
Text of figure above: "Fig. 1 Gibberellin suppresses floral transition in J. curcas. (A) Four-month-old seedlings of control plants were grown in the greenhouse; scale bar = 1 m. (B) Four-month-old plants treated with 1 g of GA4. GA4 powder was added to the soil before planting; bar = 1 m. (C) Four-month-old seedlings treated with 1 g of 25% PAC. 25% PAC powder was mixed into the soil before planting. The insects provide a close-up view of the inflorescences. Bar = 10 cm for plants. Bar = 1 cm for inflorescences. (D-E) Flowering time and number of leaves on the main stem at flowering. (F) The heights of one-year-old trees were analyzed for the control and for those plants treated with GA (+GA) or PAC (+PAC). "
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A tomato NAC transcription factor, SlNAP1, directly regulates gibberellin-dependent fruit ripening  

A tomato NAC transcription factor, SlNAP1, directly regulates gibberellin-dependent fruit ripening   | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it

Authors: Changxia Li, Xuemei Hou, Zongxi Zhao, Huwei Liu, Panpan Huang, Meimei Shi, Xuetong Wu, Rong Gao, Zhiya Liu, Lijuan Wei, Yihua Li and Weibiao Liao.


Cellular & Molecular Biology Letters (2024)


Abstract: "In tomato (Solanum lycopersicum), the ripening of fruit is regulated by the selective expression of ripening-related genes, and this procedure is controlled by transcription factors (TFs). In the various plant-specific TF families, the no apical meristem (NAM), Arabidopsis thaliana activating factor 1/2 (ATAF1/2), and cup-shaped cotyledon 2 (CUC2; NAC) TF family stands out and plays a significant function in plant physiological activities, such as fruit ripening (FR). Despite the numerous genes of NAC found in the tomato genome, limited information is available on the effects of NAC members on FR, and there is also a lack of studies on their target genes. In this research, we focus on SlNAP1, which is a NAC TF that positively influences the FR of tomato. By employing CRISPR/Cas9 technology, compared with the wild type (WT), we generated slnap1 mutants and observed a delay in the ethylene production and color change of fruits. We employed the yeast one-hybrid (Y1H) and dual-luciferase reporter (DLR) assays to confirm that SlNAP1 directly binds to the promoters of two crucial genes involved in gibberellin (GA) degradation, namely SlGA2ox1 and SlGA2ox5, thus activating their expression. Furthermore, through a yeast two-hybrid (Y2H), bimolecular fluorescence complementation (BIFC) and luciferase (LUC) assays, we established an interaction between SlNAP1 and SlGID1. Hence, our findings suggest that SlNAP1 regulates FR positively by activating the GA degradation genes directly. Additionally, the interaction between SlNAP1 and SlGID1 may play a role in SlNAP1-induced FR. Overall, our study provides important insights into the molecular mechanisms through which NAC TFs regulate tomato FR via the GA pathway."

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The JA-OsJAZ6-DELLA module controls the tillering and drought stress response in rice

The JA-OsJAZ6-DELLA module controls the tillering and drought stress response in rice | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it
Authors: Wanmin Wang, Zizhao Xie, Yuanyuan Wu, Ying Sun, Chenghang Zhan, Liang Jin and Junli Huang. 

Environmental and Experimental Botany (2024)

Highlights: • OsJAZ6 modulates rice tillering and drought response by integrating JA with GA signaling. • OsJAZ6 controls the tiller bud growth but not formation. • OsJAZ6 interacts with SLR1 to promote its degradation, which further destabilizes MOC1. • OsJAZ6 and SLR1 have opposite functions in regulating rice tiller bud growth and drought tolerance. 

Abstract: "Jasmonic acid (JA) plays crucial functions during plant growth and stress response, but its roles and regulatory mechanism in plant branching remain largely unknown. Rice basal branching (tillering) is an essential agronomic trait that affects crop production. Here, we report that OsJAZ6, the repressor of JA signaling, negatively modulates rice tillering and drought stress tolerance. Loss-of-function mutants of OsJAZ6 exhibit a significant increase in tiller number, while OsJAZ6ΔJas-overexpression lines produce fewer tillers than wild-type plants. Further investigations show that function loss of OsJAZ6 promotes the tiller bud growth rather than formation. Mechanistic studies show that OsJAZ6 interacts with rice DELLA/SLR1 (SLENDER RICE 1), a transcription repressor of gibberellin (GA) signaling, and the interaction promotes SLR1 degradation, which further facilitates the degradation of rice tillering regulator MOC1 (MONOCULM 1), thereby inhibiting the tiller bud growth. In agreement, the slr1 mutant exhibits fewer tillers than wild type. Consistently, application of JA promotes the growth of tiller bud and thus increases the tiller number, while GA treatment results in opposite result. Meanwhile, osjaz6 mutants display enhanced drought tolerance, coupled with increased JA sensitivity, while the slr1 mutant shows the reverse behavior. Collectively, our data demonstrate that OsJAZ6 negatively modulates rice tillering as well as drought stress tolerance by destabilizing SLR1 protein. Our data shed light on the regulatory mechanism of controlling the tiller development and drought stress response in rice by the JA-OsJAZ6-SLR1 module."
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A hemizygous supergene controls homomorphic and heteromorphic self-incompatibility systems in Oleaceae

A hemizygous supergene controls homomorphic and heteromorphic self-incompatibility systems in Oleaceae | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it
Authors: Pauline Raimondeau, Sayam Ksouda, William Marande, Anne-Laure Fuchs, Hervé Gryta, Anthony Theron, Aurore Puyoou, Julia Dupin, Pierre-Olivier Cheptou, Sonia Vautrin, Sophie Valière, Sophie Manzi, Djamel Baali-Cherif, Jérôme Chave, Pascal-Antoine Christin and Guillaume Besnard.

Current Biology (2024)

Editor's view: Raimondeau et al. unveil the genetic determinants of the unique self-incompatibility system of olives. This initial discovery leads them to identify the genetic controls of distyly within the family and to uncover a genetic overlap between the two systems, rooted in shared ancestry.

Highlights: • Homomorphic self-incompatibility in olives is associated with a hemizygous region • A homologous hemizygous region is also involved in controlling distyly in jasmine • The duplication of this DNA segment is ancestral in the family • Hormonal regulation is central to the production of self-incompatibility phenotypes

Abstract: "Self-incompatibility (SI) has evolved independently multiple times and prevents self-fertilization in hermaphrodite angiosperms. Several groups of Oleaceae such as jasmines exhibit distylous flowers, with two compatibility groups each associated with a specific floral morph.1 Other Oleaceae species in the olive tribe have two compatibility groups without associated morphological variation.2,3,4,5 The genetic basis of both homomorphic and dimorphic SI systems in Oleaceae is unknown. By comparing genomic sequences of three olive subspecies (Olea europaea) belonging to the two compatibility groups, we first locate the genetic determinants of SI within a 700-kb hemizygous region present only in one compatibility group. We then demonstrate that the homologous hemizygous region also controls distyly in jasmine. Phylogenetic analyses support a common origin of both systems, following a segmental genomic duplication in a common ancestor. Examination of the gene content of the hemizygous region in different jasmine and olive species suggests that the mechanisms determining compatibility groups and floral phenotypes (whether homomorphic or dimorphic) in Oleaceae rely on the presence/absence of two genes involved in gibberellin and brassinosteroid regulation."
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This relevant article is posted together with the one by Castric et al. ("The homomorphic self-incompatibility system in Oleaceae is controlled by a hemizygous genomic region expressing a gibberellin pathway gene").
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PdRabG3f interfered with gibberellin-mediated internode elongation and xylem developing in poplar

PdRabG3f interfered with gibberellin-mediated internode elongation and xylem developing in poplar | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it
Authors: Jiujun Du, Hantian Wei, Xueqin Song, Lei Zhang and Jianjun Hu. 

Plant Science (2024)

Highlights: • PdRabG3f inhibited the vertical elongation of poplar by suppressing internode elongation. • PdRabG3f inhibited xylem development by suppressing cambium division and differentiation. • PdRabG3f interfered with gibberellin-mediated internode elongation and xylem developing in poplar. 

Abstract: "As a member of the small GTPases family, Rab GTPases play a key role in specifying transport pathways in the intracellular membrane trafficking system and are involved in plant growth and development. By quantitative trait locus (QTL) mapping, PdRabG3f was identified as a candidate gene associated with shoot height in a hybrid offspring of Populus deltoides ‘Danhong’ × Populus simonii ‘Tongliao1’. PdRabG3f localized to the nucleus, endoplasmic reticulum and tonoplast and was primarily expressed in the xylem and cambium. Overexpression of PdRabG3f in Populus alba × Populus glandulosa (84 K poplar) had inhibitory effects on vertical and radical growth. In the transgenic lines, there were evident changes in the levels of 15 gibberellin (GA) derivatives, and the application of exogenous GA3 partially restored the phenotypes mediated by GAs deficiency. The interaction between PdRabG3f and RIC4, which was the GA-responsive factor, provided additional explanation for PdRabG3f's inhibitory effect on poplar growth. RNA-seq analysis revealed differentially expressed genes (DEGs) associated with cell wall, xylem, and gibberellin response. PdRabG3f interfering endogenous GAs levels in poplar might involve the participation of MYBs and ultimately affected internode elongation and xylem development. This study provides a potential mechanism for gibberellin-mediated regulation of plant growth through Rab GTPases."
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Revisit and explore the ethylene-independent mechanism of sex expression in cucumber (Cucumis sativus)  

Authors: Nguyen Hoai Nguyen, Phuong Thi Bich Ho and Linh Thi Truc Le.


Plant Reproduction (2024)


Key message: This review provides a thorough and comprehensive perspective on the topic of cucumber sexual expression. Specifically, insights into sex expression mediated by pathways other than ethylene are highlighted. 


Abstract: "Cucumber (Cucumis sativus L.) is a common and important commercial crop that is cultivated and consumed worldwide. Additionally, this species is commonly used as a model for investigating plant sex expression. Cucumbers exhibit a variety of floral arrangements, comprising male, female, and hermaphroditic (bisexual) flowers. Generally, cucumber plants that produce female flowers are typically preferred due to their significant impact on the overall output. Various environmental conditions, such as temperature, light quality, and photoperiod, have been also shown to influence the sex expression in this species. Multiple lines of evidence indicate that ethylene and its biosynthesis genes are crucial in regulating cucumber sex expression. Gibberellins, another well-known phytohormone, can similarly influence cucumber sex expression via an ethylene-independent route. Further studies employing the next-generation sequencing technology also visualized a deeper slice of the molecular mechanism such as the role of the cell cycle program in the cucumber sex expression. This review aims to provide an overview of the sex expression of cucumber including its underlying molecular mechanism and regulatory aspects based on recent investigations."

Julio Retamales's insight:
Text of figure above: "The GA phytohormones antagonistically regulate the sex expression (namely, female flower formation) in cucumber. GA can suppress the ethylene biosynthesis and signaling pathways to control the cucumber sex expression. In addition, GA may also regulate this biological phenomenon via an ethylene-independent pathway (via downstream factors including CsGAMYB1 and CsCAG2)"
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Ascorbic acid releases dormancy and promotes germination by an integrated regulation of abscisic acid and gibberellin in Pyrus betulifolia seeds

Ascorbic acid releases dormancy and promotes germination by an integrated regulation of abscisic acid and gibberellin in Pyrus betulifolia seeds | Plant hormones (Literature sources on phytohormones and plant signalling) | Scoop.it
Authors: Junpeng Niu, Mingzhen Xu, Na Zong, Jia Sun, Lei Zhao and Wei Hui. 

Physiologia Plantarum (2024)

Abstract: "Seed dormancy is an important life history state in which intact viable seeds delay or prevent germination under suitable conditions. Ascorbic acid (AsA) acts as a small molecule antioxidant, and breaking seed dormancy and promoting subsequent growth are among its numerous functions. In this study, a germination test using Pyrus betulifolia seeds treated with exogenous AsA or AsA synthesis inhibitor lycorine (Lyc) and water absorption was conducted. The results indicated that AsA released dormancy and increased germination and 20 mmol L−1 AsA promoted cell division, whereas Lyc reduced germination. Seed germination showed typical three phases of water absorption; and seeds at five key time points were sampled for transcriptome analysis. It revealed that multiple pathways were involved in breaking dormancy and promoting germination through transcriptome data, and 12 differentially expressed genes (DEGs) related to the metabolism and signal transduction of abscisic acid (ABA) and gibberellins (GA) were verified by subsequent RT-qPCR. For metabolites, exogenous AsA increased endogenous AsA and GA3 but reduced ABA and the ABA/GA3 ratio. In addition, three genes regulating ABA synthesis were downregulated by AsA, while five genes mediating ABA degradation were upregulated. Taken together, AsA regulates the pathways associated with ABA and GA synthesis, catalysis, and signal transduction, with subsequent reduction in ABA and increase in GA and further the balance of ABA/GA, ultimately releasing dormancy and promoting germination."
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In preprints: hormonal stepping stones to diverging root organogenesis 

Authors: Clare Hurst and Miriam L. Gifford.


Development (2024)


Excepts: "Legumes form a symbiotic relationship with bacteria called rhizobia. The rhizobia fix atmospheric dinitrogen, which is used by the plant as a nitrogen resource, and take up molecules, including carbon compounds, from the plant. Rhizobia are housed in nodules that develop on roots after a series of orchestrated stages that are triggered by the perception and entry of rhizobia at root hairs (reviewed by Luo et al., 2023). Study of this relationship and the mechanisms that govern nodule formation and inhibition may reveal targets to promote enhanced nodulation efficiency and increased nitrogen acquisition for the plant. Phytohormones have been shown to play a key role in both nodule formation and inhibition; therefore, a better understanding of hormonal regulatory activity could provide options for such enhancement. To address this, Drapek and colleagues (2023 preprint) focus on the dynamics of gibberellin (GA), a phytohormone previously identified as both a positive and negative regulator of nodulation (Rizza et al., 2017; Fonouni-Farde et al., 2016).


 "In conclusion, this study analysed the spatial and temporal accumulation of GA, the interactions between GA and key nodule identity regulatory genes, and tested the importance of GA biosynthesis enzymes in nodule formation. The work provides strong evidence that GA is a potential determinator between lateral root formation and nodulation, and helps to explain previous contradictory findings related to the importance of GA, as well as cytokinin, in these processes."

Julio Retamales's insight:
Commentary on the relevant article  by Drapek et al. ("Cellular gibberellin dynamics govern indeterminate nodule development, morphology and function"), which was already posted here and is to be found at:


Figure shown above is from the original article by Drapek et al. whose full text is: "Fig.1 – GA accumulates early in nodule development and persists in the nodule apex. 122 (a) Emission ratio of LjUBQp::nlsGPS2 in M. truncatula root (top panel) and YFP control (bottom panel), N ≥ 20. (b-d) Emission ratio of nlsGPS2 and YFP/Brightfield channel overlay in M. truncatula nodules inoculated with Sm2011. (b) 4 dpi nodule primordia embedded in 4.5% agarose and sliced in 100μm sections, N=3. White arrowhead indicates cortex, white arrow indicates endodermis/stele, yellow arrowhead indicates epidermis. (c) 5 dpi whole mount nodule primordia, N ≥ 20. (d) 2 wpi nodule embedded 4.5% agarose and sliced in 100μm sections, N ≥ 20. (e) Emission ratio of nuclei (individual dots) from whole mount nodules at 5 dpi as a function of distance from nodule center, N=9. Curves of best fit are computed in R using a generalized additive model via ggplot. (f) Quantification of emission ratio of nuclei (individual dots) of 2 wpi nodules as a function of distance from nodule tip, N=5. Curves of best fit are computed in R using a generalized additive model via ggplot. Bars = 100 μm in (a,c,d); Bar = 50μm in (b)." 
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