Plant Science Research Weekly: May 3, 2024

Review: The plant immune system: From discovery to deployment

A review of the past 50 years of plant immunity by Jones, Staskawicz, and Dangl? Yes please! I particularly enjoy historical perspectives of a discipline, as they frame conceptual breakthroughs with the benefit of hindsight. As the article lays out, understanding the plant immune system benefitted greatly from the early advances in plant molecular biology and gene cloning, which allowed established concepts to be linked to proteins. Over a short period of time, several receptor proteins and pathogen effectors were identified, leading to the two-step model of cell-surface pattern-triggered immunity, backed up by intracellular effector-triggered immunity. This simple model has provided a structure that encompasses an extraordinary degree of nuance and subtlety, spurred in part by advances in structural analysis, sequencing, phylogenomics, and metagenomics. The authors conclude with a list of questions they would like to see solved in the next 20 years. Ultimately, it is the application of this knowledge to crop plants to enhance global food security that really matters, and this will be helped by CRISPR-based genome editing tools as well as an enlightened public who understand how today’s technology to support plant immunity connects to classical breeding; this article does an excellent job of bridging that gap. (Summary by Mary Williams @PlantTeaching) Cell 10.1016/j.cell.2024.03.045

Perspective: Exposing belowground plant communication

Plants possess a fascinating ability to communicate with each other through a complex system of chemical signals. Aboveground, they use airborne volatile signals to attract predatory insects, prime defenses in neighbors, facilitate nutrient transfer, and promote plant interactions. However, less is known about the chemical signaling that goes on underground. In this Perspective article, Guerrieri and Rasmann highlight what is known and unknown about belowground plant communication. As they suggest, soil matrix communication provides an efficient way to rapidly respond to biotic and abiotic stresses and can contribute to ecosystem processes. The authors provide examples of ways that root exudates communicate important information between organisms. Plants can also communicate through mycorrhizal networks to transfer available resources and signal between interconnected plants. However, understanding belowground plant communication calls for methodological advances, including sampling and characterizing root exudates in natural environments. Untargeted metabolomics and machine learning algorithms can detect molecules produced by roots under different stress conditions. Understanding and applying the potential of root exudates can be a game changer for sustainable agriculture and cost-effective ecosystem management. (Summary by Maneesh Lingwan, @LingwanManeesh) Science 10.1126/science.adk1412

Review: The genomic route to tomato breeding: Past, present, and future

Widely and abundantly eaten tomatoes (Solanum lycopersicum) are delicious and nutritious, but the genetic diversity of cultivated tomatoes is quite narrow. In this review, Wang et al. give an overview of efforts to increase diversity, through introduction of genes from wild relatives and other approaches. Since the first tomato sequence was completed in 2012, countless sequences have been obtained from various cultivars and wild relatives, capturing the inter- and intra-species diversity. As a commercially important crop, tomatoes have been extensively analyzed for metabolic, developmental, resilience, and consumer preference traits, which have been mapped to genes and loci; there’s no shortage of data about tomatoes. Key traits that have been mapped pertain to flowering time, disease resistance, fruit weight, shape, ripening and quality. All this information provides the opportunity to produce exceptional varieties, but this is hindered by slow pace of conventional breeding. New technologies to accelerate breeding  include haploid and male sterility breeding, heterosis, de novo domestication, gene editing, synthetic biology, and AI-assisted approaches.  (Summary by Mary Williams @PlantTeaching) Plant Physiol. 10.1093/plphys/kiae248

Phylogenomic insights into angiosperm evolution

Low-resolution data can provide broad strokes but miss the details that come from greater information density. When striving to understand the multimillion-year evolutionary history of the angiosperms, more data certainly helps. Here, by focusing on a subset of 353 genes, Zuntini and Carruthers et al. present a phylogenomic tree that increases the number of represented angiosperm genera by fifteen-fold and includes all 416 families. The dataset encompasses 7,923 angiosperm genera, is time-calibrated through the analysis of a 200 fossil dataset, and enriched by samples from 163 herbaria in 48 countries. What does all this effort reveal? The results are beautifully presented in Figure 1 (available for download as a very high-resolution image, if, like me, you’d like to print it as a poster). Several clades have been reassigned, split, or lumped thanks to the new deeper dataset. The full dataset highlights two periods of exceptional diversification in the angiosperms; the first shortly after they emerged, during which about 80% of extant orders originated, and the second about 40 million years ago. The paper includes an Inclusion and Ethics statement, in which the authors acknowledge the people who collected and curated these samples and the complex histories underlying natural history collections. (Summary by Mary Williams @PlantTeaching) Nature 10.1038/s41586-024-07324-0

 Genomics from bean to cup: New insights into the history of Arabica coffee diversification

As one of the most traded commodities in the world, coffee has cultural and economic impact that spans continents. The main source of coffee beans, Coffea arabica (Arabica), is a polyploid species that resulted from the hybridization between diploid C. canephora (Robusta) and C. eugenioides (Eugenioides). Here, Salojärvi et al. produce chromosome-level assemblies of all three species, and reveal kinship and population dynamics estimates for 41 wild and cultivated coffee cultivars. No clear dominance expression pattern was observed between the Robusta- and Eugenioides-derived subgenomes of C. arabica. The overall low genetic diversity found in C. arabica, evidenced by its susceptibility to diseases such as leaf rust, is attributed to its relatively recent polyploid origin, estimated at 610-350 thousand years ago (ka). Population parameters point to a long bottleneck event (350-30.5 ka) ending with a more favourable climate for coffee growth and the split between today’s wild and cultivated populations. Migration across the split ended at ca. 9 ka, with wild populations alone facing another bottleneck, while cultivated Arabica spread to Yemen. In fact, Arabica cultivation is documented in Yemen in the 15th and 16th centuries, from where a handful of seeds made it to India; cultivation soon spread across Asian Dutch colonies. Some plants were brought to Europe and then spread by colonizers even more widely, notably from the island of Bourbon (present-day Réunion). Genomic data further documents the history of coffee: early Indian cultivar JK1 and later Typica and Bourbon cultivar groups are estimated to all share close kinship, reinforcing their ultimately Yemeni origin. Through natural hybridization with Robusta, a group of Timor Arabica cultivars are resistant to leaf rust. The Robusta introgression shared by resistant hybrids comprises blocks of candidate resistance genes that will be valuable tools in breeding strategies for leaf rust-resistant Arabica. (Summary by John Vilasboa @vilasjohn) Nat. Genet.  10.1038/s41588-024-01695-w

Genetic gains underpinning a little-known strawberry Green Revolution

The domestication of cultivated strawberry (Fragaria × ananassa) traces back approximately 300 years, providing us with a relatively comprehensive genealogy of this artificial hybrid species. Strawberry yield in the US has increased by 2,755% since the 1960’s, largely owing to the California strawberry Green Revolution. Through an analysis of California strawberry germplasm, researchers have pinpointed significant factors contributing to this remarkable increase. One crucial contributor was the introduction of photoperiod-insensitive, PERPETUAL FLOWERING hybrids during the 1970s, which substantially enhanced yield potential. Additionally, the adoption of methyl bromide fumigation played a pivotal role by significantly reducing yield losses attributed to diseases. However, the widespread use of fumigation has led to a decline in resistance among contemporary strawberry accessions to soil-borne pathogens such as Verticillium wilt and Phytophthora crown rot. This poses a potential threat to strawberry production in the US, especially with the phasing out of methyl bromide. (Summary by Villő Bernád) Nature Comms. 10.1038/s41467-024-46421-6

Enhanced super-resolution ribosome profiling unveils pervasive translation of upstream ORFs and small ORFs in Arabidopsis

In recent years, the discovery that the translational regulation of many mRNAs is influenced by small upstream open reading frames (uORFs) has highlighted the importance of precisely identifying gene structures and translated ORFs to understand gene functions and cellular behavior. Using Arabidopsis, Wu et al. advanced the precision of ribosome profiling, in which RNA sequences bound by ribosomes are identified, revealing 7,751 unconventional translation occurrences. Subsequent validation via proteomic scrutiny affirmed the production of stable proteins from the identified sites. Noteworthy instances of active translation were observed in small interfering RNAs and microRNAs. A novel methodology was developed to discern short upstream ORFs (uORFs), showcasing distinct translational repression patterns. Moreover, the recognition of 594 uORFs regulated through alternative splicing, and their involvement in crucial pathways, underscores the comprehensive nature of this investigation in elucidating the mechanisms governing gene expression regulation in Arabidopsis. (Summary by Yueh Cho @YuehCho1984) Plant Cell. 10.1093/plcell/koad290.

Heat stress promotes Arabidopsis AGO1 phase separation and association with stress granule components

A new article by Blagojevic, Baldrich, and Schiaffini et al. reveals that Arabidopsis ARGONAUTE1 (AGO1) protein, a pivotal agent in miRNA and siRNA-mediated gene silencing associated with the rough endoplasmic reticulum, dynamically localizes within stress granule components during heat stress (HS). This relocalization does not require SUPPRESSOR OF GENE SILENCING 3 (SGS3) and includes interactions with P-bodies and RNA decay components, forming a unique HS-induced AGO1 interactome. Moreover, even a short period of HS at 37°C results in only limited changes to small RNA (sRNA) accumulation and their loading into AGO1, indicating the resilience of AGO1’s silencing capabilities under HS. A significant finding is that AGO1 undergoes liquid-liquid phase separation through its N-terminal Poly-Q domain, which may contribute to its protective aggregation in cytosolic condensates. This study enhances our understanding of the molecular responses to HS in plants, highlighting the robust nature of AGO1 and its gene regulatory functions during environmental stress. (Summary by Yueh Cho @YuehCho1984) iScience. 10.1016/j.isci.2024.109151

Conjugation of ATG8 to vacuolar membranes as a response to cell wall damage

ATG8 is a well-characterized protein involved in autophagy that binds to the double-membrane enclosed phagophore. In a new preprint, Julian et al. explore their finding that ATG8 binds to the single-membrane enclosed vacuolar membrane (tonoplast). They observed that this binding is enhanced by treatments that weaken the cell wall, such as inhibition of cellulose synthase. To identify its function, they generated plants defective in conjugation of ATG8 to single membranes (ΔCASM), which blocks this specific interaction but does not affect autophagy more broadly. ΔCASM plants show defects in tonoplast and vacuolar integrity and are more sensitive to cell-wall damage. The authors propose a vacuolar quality control (VQC) pathway in which cell wall damage triggers a change in turgor pressure and vacuolar pH which leads to ATG8 recruitment and membrane remodeling to prevent tonoplast lysis in conditions where cell wall integrity is damaged. This work has identified a new quality control pathway for vacuoles and links ATG8 with cell integrity sensing. (Summary by Mary Williams @PlantTeaching) bioRxiv  10.1101/2024.04.21.590262

Photoperiod-insensitive flowering is associated with the FT gene in hemp

Cannabis sativa, also known as hemp or marijuana, is a widely cultivated plant for a variety of reasons. It is perhaps best known as a producer of an intoxicating chemical, THC, produced by glandular trichomes on female flowers, but low-THC producers (hemp) are cultivated for fibers. Flowering time affects both THC and fiber production, and various cultivars have a wide range of flowering-time responses. Here, Dowling et al. explored the genetic basis for photoperiod insensitive flowering time in the cultivar FINOLA. They identified a candidate locus, Autoflower2, that includes a tandem duplication of CsFT1, an ortholog of FLOWERING LOCUS T (FT). Interestingly, in photoperiod sensitive cultivars, this gene exists in a single copy. Furthermore, the expression of the genes in FINOLA is photoperiod insensitive, whereas it is only expressed in flower-inducing conditions in photoperiod sensitive cultivars. The authors surveyed a population of cultivars and found a correlation with the FINOLA-type CsFT1 locus and photoperiod insensitivity, although other genes are likely to contribute as well. (Summary by Mary Williams @PlantTeaching) Plant J. 10.1111/tpj.16769

Significant floral diversity independent of pollinator change in ‘Buzz-Bee’ pollinated Melastomataceae

The concept of pollination syndromes posits that floral diversity arises from shifts among pollinator groups, yet their predictive accuracy for pollinator identification is debated. Kopper et al. leveraged machine learning, utilizing 44 floral traits from 252 species with known pollinator interactions, to predict pollinators for 159 species lacking empirical data. Concurrently, they used multivariate and phylogenetic analyses to examine the link between pollinator shifts and floral disparity within Melastomataceae, a diverse family of flowering plants found mainly in tropical regions. The findings confirmed four distinct pollination syndromes and revealed that, while pollinator transitions contribute to floral diversity, the greatest disparity was observed in the species-rich ‘buzz-bee’ syndrome, suggesting that significant floral variation can develop without pollinator shifts. Buzz-pollinated flowers release pollen only when bees apply specific vibrations to the flower, and in many families buzz-pollinated species show similar flower morphologies. Additionally, species-poor clades and certain regions also significantly contributed to floral diversity. Overall, their study underscores the potential of machine learning in evaluating pollination syndromes and predicting pollinators where direct evidence is unavailable. (Summary by Yueh Cho @YuehCho1984) New Phytologist. 10.1111/nph.19735

Cyanobacterial PSI assembly

Dai, Song, Xu et al. identify Ycf51 as a photosystem I assembly factor in cyanobacteria

https://doi.org/10.1093/plcell/koad330

By Guo-Zheng Dai, Central China Normal University

Question: Background: While the mechanisms of photosystem II biogenesis and the auxiliary proteins involved are well known, we know much less about photosystem I (PSI) assembly. Several PSI assembly factors exist only in plants but not in cyanobacteria (the presumptive ancestors of present-day chloroplasts), suggesting that there are differences in PSI assembly between cyanobacteria and plants. The initial aim of this study was to screen 12 hypothetical chloroplast reading frames (ycfs) that are conserved in Synechocystis sp. PCC 6803 for additional players in photosynthesis. This screen led to the identification of Ycf51 (Sll1702), a thylakoid membrane protein involved in Synechocystis PSI assembly.

Questions: How does ycf51 disruption affect PSI formation? What is the role of Ycf51 in PSI formation in cyanobacteria?

Findings: Ycf51 specifically localizes to thylakoid membranes, and its hydrophilic C terminus is exposed to the stroma. ycf51 disruption in Synechocystis leads to a strong decrease in PSI content, which impairs photoautotrophic growth. Ycf51 mediates PSI complex biogenesis at the post-translational level, while its disruption has little effect on PSI stability. Ycf51 cooperates with the PSI assembly factor Ycf3, but its absence does not negatively impact Ycf3 stability. Ycf51 also interacts with the PSI subunit PsaC, indicating its direct participation in PSI assembly.

Next steps: Future studies will aim to identify the PSI assembly intermediate, whose formation requires Ycf51 function, and to elucidate the interplay of the different accessory factors involved in cyanobacterial PSI assembly.

Reference:

Guo-Zheng Dai, Wei-Yu Song, Hai-Feng Xu, Miao Tu, Chen Yu, Zheng-Ke Li, Jin-Long Shang, Chun-Lei Jin, Chao-Shun Ding, Ling-Zi Zuo, Yan-Ru Liu, Wei-Wei Yan, Sha-Sha Zang, Ke Liu, Zheng Zhang, Ralph Bock, Bao-Sheng Qiu. (2024). Hypothetical chloroplast reading frame 51 encodes a photosystem I assembly factor in cyanobacteria. https://doi.org/10.1093/plcell/koad330

Maintaining pollen tube integrity in maize

Zhou et al. investigated pollen tube integrity maintenance mechanisms in maize. The Plant Cell (2023) https://doi.org/10.1093/plcell/koad324

By Liang-Zi Zhou and Thomas Dresselhaus

Background: As sperm cell transporting vehicles, pollen tubes of flowering plants grow through the transmitting tissues of the style to delivery immobile sperm cells for double fertilization and seed production. In maize (Zea mays), pollen tubes grow up to 1 cm per hour through elongated styles (silks) before their sperm cell cargo is released inside ovules. In the model plant Arabidopsis (Arabidopsis thaliana), it has been shown that pollen tube secreted RALF proteins interact with receptor complexes and cell wall proteins to regulate pollen tube integrity during pollen germination and tube growth. Whether the identified mechanisms exist in other flowering plants was not known.

Question: Are the mechanisms that regulate pollen tube integrity evolutionarily conserved among flowering plants? We addressed this question by using maize, as a grass and crop species that has sexual organs with very different morphology from those of Arabidopsis.

Findings: Based on phylogenetic analysis, RALF proteins from maize and Arabidopsis can be classified into different clades. We show that maize Clade IB ZmRALFs are mainly located in the pollen tube cell wall and are required for proper pollen tube growth. ZmRALFs from Clade IB, but not ZmRALFs form Clade III, strongly interact as ligands with cell surface receptor-like kinases, co-receptors, and cell wall proteins from both maize and Arabidopsis. The strongest binding affinity was observed with LRX/PEX cell wall proteins. Mis-regulation of Clade IB RALFS affected pectin patterning of the pollen tube cell wall. In summary, our findings indicate that Clade IB RALF signaling mechanisms are partly conserved between both species, and that RALF proteins play a dual role as cell wall component and extracellular sensors in regulating cell wall integrity.

Next steps: It is now important to identify and study components of RALF downstream signaling and to establish the dual role of RALF interaction/competition between cell wall proteins and cell surface receptors. Moreover, the function of pollen tube-specific RALFs of Clade III that are not located to the cell wall remains to be elucidated to better unravel the multiple roles of this protein family during pollen tube growth.

Reference:

Liang-Zi Zhou, Lele Wang, Xia Chen, Zengxiang Ge, Julia Mergner, Xingli Li, Bernhard Küster, Gernot Längst, Li-Jia Qu and Thomas Dresselhaus. (2023). The RALF signaling pathway regulates cell wall integrity during pollen tube growth in maize. https://doi.org/10.1093/plcell/koad324

Variegated Canvases: The Diverse World of Plant Shoot Stem Cells

Bradamante et al. investigate the heterogeneity of stem cells of the shoot apical meristem

https://doi.org/10.1093/plcell/koad295

By Vu Nguyen, Gabriele Bradamante, Ortrun Mittelsten Scheid and Ruben Gutzat

Background: In plants, stem cells in the shoot apical meristem (SAM) produce new organs such as leaves and flowers. Transposons are parasitic, self-replicating genetic elements and evolutionary theory predicts that transposons are active in stem cells, allowing them to be transmitted to the next generation. Transposon activity can damage the cell’s genome and therefore, plants also deploy cellular defenses against the propagation of transposons. Among these defenses are epigenetic mechanisms involving ARGONAUTE (AGO) proteins and small RNAs, with AGO5 and AGO9 showing high abundance in SAM stem cells.

Question: This study delves into the roles of AGO5 and AGO9 throughout plant development, particularly their potential in safeguarding meristem cells from transposon activity.

Findings: Investigating AGO5 and AGO9 expression through various stages of plant development, the study unveils surprising dynamics within SAM stem cells, especially in the subepidermal layer, which provides the progenitors for reproductive cells. These cells also exhibit heightened activity of potentially dangerous transposons. Furthermore, these transposons are processed into small RNAs by the cell and loaded onto AGO5 and AGO9. This resembles a genomic conflict between the host genome and transposons, similar to observations in animal reproductive cells. This is also evidence for the presence of a specialized group of reproductive cells within the meristem from an early developmental stage.

Next step: These insights into the variability of SAM stem cells pave the way for in-depth research on transposon behavior and gene control within these cells. Future studies could extend to examining transposon control through generations, particularly under environmental stresses like elevated temperatures.

Reference:

Gabriele Bradamante, Vu Hoang Nguyen, Marco Incarbone, Zohar Meir, Heinrich Bente, Mattia Donà, Nicole Lettner, Ortrun Mittelsten Scheid, Ruben Gutzat (2024) Two ARGONAUTE proteins loaded with transposon-derived small RNAs are associated with the reproductive cell lineage in Arabidopsis https://doi.org/10.1093/plcell/koad295

Epitranscriptional regulation of salicylic acid signaling

Lee, Liu, Kim et al. demonstrate that a plant m6A reader dampens stress responses.

By Keun Pyo Lee, Kaiwei Liu, Eun Yu Kim, and Chanhong Kim

CAS Center for Excellence in Molecular Plant Sciences (CEMPS), Chinese Academy of Sciences (CAS)

https://doi.org/10.1093/plcell/koad300

Background: mRNAs undergo various modifications. N6-methyladenosine (m6A) is the most prevalent epigenetic modification in eukaryotic mRNAs. A network of enzymes called m6A “writers” and “erasers” reversibly regulates this modification, affecting various aspects of mRNA metabolism through proteins called m6A “readers”. m6A readers contain the YTH domain responsible for m6A binding. The m6A modification plays pivotal roles in plant physiological responses, including growth, development, and stress responses. However, the biological significance of m6A readers and their mode of action in mRNA metabolism are largely unknown. Moreover, unlike in animals and yeast, many m6A readers in plants have yet to be identified.

Question: Based on our previous finding that multiple YTH family proteins interact with LESION SIMULATING DIEASE1 (LSD1), a negative regulator of salicylic acid (SA)-induced cell death, we sought to uncover their roles as SA-responsive m6A readers and their impact on SA-driven stress responses in Arabidopsis (Arabidopsis thaliana).

Findings: Among the 13 YTH family proteins in Arabidopsis, we identified EVOLUTIONARILY CONSERVED C-TERMINAL REGION1 (ECT1) as a crucial player in SA-mediated stress responses. Loss of ECT1 enhances SA-primed growth retardation and cell death. ECT1 undergoes liquid-liquid phase separation, forming cytosolic biomolecular condensates such as processing bodies and stress granules, sites for decay and/or storage of non-translating mRNAs, in response to SA or bacterial pathogens. It sequesters SA-induced m6A modification-prone mRNAs (SA-m6A-mRNAs), facilitating their decay in cytosolic biomolecular condensates, thus compromising SA-mediated stress responses. Arabidopsis plants overexpressing ECT1 are more susceptible to bacterial pathogens.

Next steps: Considering the phenotypic similarity between ect1 and ect2 mutants upon SA treatment, we wish to investigate the functional interplay and inter-dependency between ECT1 and ECT2 in SA-dependent plant stress responses. Moreover, apart from ECT1 function in SA-m6A-mRNA decay, we will explore its potential role in stabilizing other subsets of m6A-mRNAs, likely within stress granules.

Reference:

Keun Pyo Lee, Kaiwei Liu, Eun Yu Kim, Laura Medina-Puche, Haihong Dong, Minghui Di, Rahul Mohan Singh, Mengping Li, Shan Qi, Zhuoling Meng, Jungnam Cho, Heng Zhang, Rosa Lozano-Duran, and Chanhong Kim. (2023). The m6A reader ECT1 drives mRNA sequestration to dampen salicylic acid–dependent stress responses in Arabidopsis. https://doi.org/10.1093/plcell/koad300

Co-evolution of the RNA editing factor PPR78 and its targets

Lesch et al. reveal that the mitochondrial RNA editing factor PPR78 of Physcomitrium patens is conserved among mosses despite the loss of its two known C-to-U editing sites due to the additional editing target ccmFNeU1465RC.

 https://doi.org/10.1093/plcell/koad292

By Elena Lesch, Volker Knoop and Mareike Schallenberg-Rüdinger, IZMB – Institute for Cellular and Molecular Botany, Molecular Evolution Lab, University of Bonn

 Background: Plant-type RNA editing refers to the site-specific deamination of cytidines to uridines in organellar transcripts. Pentatricopeptide repeat (PPR) proteins of the PLS subfamily are key players in this process. In mosses, PPR editing factors consist of an RNA binding PLS-type PPR array and a C-terminal DYW-type cytidine deaminase domain. PPR78 is one of nine organellar RNA editing factors in the model moss Physcomitrium patens. It edits two mitochondrial targets to different extents: the cox1eU755SL site is edited efficiently, whereas the rps14eU137SL site is edited partially. Establishing the cox1 site is also crucial in other mosses, whereas editing of rps14eU137SL is highly variable, ranging from non-existent to very efficient.

Question: We aimed to unravel the co-evolution of PPR78 and its two target sites in mosses. What causes the variability in rps14 editing efficiency? What happens to PPR78 if its two target sites are lost due to genomic C-T conversions creating a pre-edited state?

Findings: An early species sampling was widely extended, focusing on the Hypnales (feather mosses). In this moss order, the cox1 site is pre-edited, making editing obsolete, and the rps14 site is edited inefficiently or not at all while PPR78 orthologues remain conserved in most species. A complementation study of a Physcomitrium knockout mutant with PPR78 orthologues from different mosses revealed that variable rps14 editing is defined by the proteins themselves, specifically their PPR arrays. We successfully expressed functional PPR78 in Escherichia coli. Off-target profiling helped predict a third editing target site of PPR78 in Hypnales: ccmFNeU1465RC. We functionally assigned PPR78 to the ccmFN site in bacterio, providing evidence that PPR78 is evolutionarily retained in Hypnales to serve this additional editing target.

Next steps: In future, assignments of further editing sites to PPR78 may be explored. The region responsible for variable rps14eU137SL editing capacities of PPR78 orthologues may be narrowed down to certain PPR repeats. In addition, ccmFNeU1465RC editing functionalities of PPR78 orthologues may be tested by knockout studies in another moss or heterologous expression.

Reference:

Elena Lesch, Maike Simone Stempel, Vanessa Dressnandt, Bastian Oldenkott, Volker Knoop, and Mareike Schallenberg-Rüdinger. (2023). Conservation of the moss RNA editing factor PPR78 despite the loss of its known C-to-U editing sites is explained by a hidden extra target. https://doi.org/10.1093/plcell/koad292

RPT2a regulates inflorescence meristem indeterminacy

 Yao, Wang et al. identify the mechanisms regulating inflorescence meristem determinacy in Arabidopsis.

https://doi.org/10.1093/plcell/koad249

By Wang Jinsong Yao1, Yi Peng Wang1, Jing Peng1, Pei Pei Yin1, Hengbin Gao1, Li Xu1,

Thomas Laux2, Xian Sheng Zhang1, and Ying Hua Su1

1Shandong Agricultural University.

2University of Freiburg.

 Background: While there is a rich diversity of shapes in the plant kingdom, inflorescence architecture can generally be classified into a limited number of types. For example, Brassicaceae members, such as Arabidopsis (Arabidopsis thaliana) or cabbage (Brassica oleracea), exhibit an indeterminate inflorescence architecture, whereas nightshade species, such as tomato (Solanum lycopersicum) or potato (Solanum tuberosum), display determinate inflorescences. These distinct architectures are associated with the indeterminacy of the inflorescence meristem (IM). The precise regulation of TERMINAL FLOWER1 (TFL1) expression is pivotal for governing both the architecture of the inflorescence and the indeterminacy of the IM. However, the mechanisms responsible for controlling TFL1 expression in this context have remained elusive.

Question: What are the mechanisms controlling the activity of the IM identity gene TFL1, thereby specifying the indeterminate nature of the Arabidopsis inflorescence? What is the role of protein degradation in directing inflorescence architecture in Arabidopsis?

Findings: We present insights into the mechanisms that fine-tune the activity of TFL1, a key regulator of indeterminate inflorescence growth in Arabidopsis. Our findings demonstrate that TFL1 levels in the IM are regulated by DNA methylation mediated by the DNA methyltransferase MET1. Low MET1 levels are maintained through proteolysis via the 26S proteasome subunit RPT2a, which keeps methylation at the TFL1 promoter low, thus promoting IM indeterminacy and indeterminate inflorescence architecture. Conversely, when RPT2a-mediated proteolysis of MET1 is hindered, TFL1 expression levels decrease, leading to a determinate zigzag-shaped inflorescence architecture. Our findings propose an integrative model that explains how proteolytic activity balances the epigenetic regulation of TFL1 expression, ultimately leading to indeterminate inflorescence architecture in Arabidopsis.

 Next Steps: We plan to explore these diverse models in other plant species, aiming to expand our knowledge regarding the genetic mechanisms governing the wide range of inflorescence architectures observed in nature.

Reference:

Wang Jinsong Yao, Yi Peng Wang, Jing Peng, Pei Pei Yin, Hengbin Gao, Li Xu, Thomas Laux, Xian Sheng Zhang and Ying Hua Su. (2023). RPT2a–MET1 axis regulates TERMINAL FLOWER1 to control inflorescence meristem indeterminacy in Arabidopsis. https://doi.org/10.1093/plcell/koad249

 

Regulatory feedback mechanisms in rice crown root development

Geng et al. reveal a feedback system that orchestrates the expression of genes controlling crown root development in rice (Oryza sativa) and uncover a molecular rheostat of this system.

https://doi.org/10.1093/plcell/koad318

By Leping Geng and Yu Zhao

National Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, 430070, China

Background: Crown roots (also called adventitious roots) are the main components of root systems in cereals and play essential roles in nutrient uptake, stress tolerance, and yield. WUSCHEL-related homeobox (WOX) and lateral organ boundaries domain (LBD) transcription factors regulate adventitious root morphogenesis in angiosperms. However, the molecular mechanisms by which these transcription factors regulate rice crown root development remain unclear.

Questions: Does LBD16 control crown root development in rice (Oryza sativa)? What is the relationship between LBD16 and WOX11 in governing rice crown root morphogenesis?

Findings: LBD16 promotes the emergence and outgrowth of crown roots in rice by influencing cell division. WOX11 recruits the histone demethylase JMJ706 that removes histone H3 lysine 9 dimethylation (H3K9me2) from the LBD16 promoter, thereby activating LBD16 transcription. More importantly, LBD16 competes with JMJ706 for interaction with WOX11 and represses its own upregulation by the WOX11–JMJ706 complex. These results reveal a feedback regulatory system controlling the expression of genes orchestrating crown root development in rice, in which LBD16 acts as a molecular rheostat.

Next steps: Root system improvement will enhance rice environmental adaptation and yield potential. Future research will focus on the underlying mechanisms mediating WOX11 recruitment of JMJ706 and removal of H3K9me2 leading to altered root architecture. Such advances would help breeders cultivate excellent varieties with ideal root systems.

Reference:

Leping Geng, Mingfang Tan, Qiyu Deng, Yijie Wang, Ting Zhang, Xiaosong Hu, Miaomiao Ye, Xingming Lian, Dao-Xiu Zhou, Yu Zhao. (2024). Transcription factors WOX11 and LBD16 function with histone demethylase JMJ706 to control crown root development in rice https://doi.org/10.1093/plcell/koad318

 背景:冠根(即不定根)是禾本科作物如水稻、小麦等根系最主要的组成成分,在营养吸收、土壤环境适应以及产量提升等方面起着重要的作用。人们发现两类重要的转录因子WOX和LBD 在被子植物不定根形态建成中发挥着关键的作用。然而,这两类转录因子调控水稻冠根发育的分子机制并不清楚。

问题:LBD调控水稻冠根发育的分子机制是什么?在调控水稻冠根发育中LBD和WOX家族蛋白的相互关系是什么?

发现:我们发现LBD16通过促进冠根原基分生组织细胞分裂而使原基伸长生长,其作用机制是WOX11招募组蛋白JMJ706去甲基化酶特异地去除LBD16启动子上的H3K9me2,从而激活LBD16的转录。更为重要的是,当细胞中LBD16蛋白增加后,就可以与JMJ706竞争性地与WOX11互作,抑制LBD16 mRNA的转录,从而维持细胞中LBD16水平的稳定。因此,我们的研究结果揭示了WOX-LBD控制水稻冠根发育的负反馈调节系统。

下一步工作计划:根系的改良有助于提高作物的环境适应性和产量。我们未来的研究将集中在该反馈系统和表观修饰因子如何相互作用促进水稻根系构型改变,为育种家培育出具有理想根系构型的水稻品种做出贡献。

Cell wall-loosening agents control fruit softening in tomato

Su et al. identify two cell wall-loosening agents that synergistically regulate tomato fruit softening.

https://doi.org/10.1093/plcell/koad291

By Guanqing Su1, Yanna Shi1, 2, 3

1College of Agriculture & Biotechnology, Zhejiang University, Zijingang Campus, Hangzhou 310058, China

2Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology, Zhejiang University, Zijingang Campus, Hangzhou, 310058, China

3The State Agriculture Ministry Laboratory of Horticultural Plant Growth, Development and Quality Improvement, Zhejiang University, Zijingang Campus, Hangzhou 310058, China.

 Background: Fruit softening is an irreversible process that occurs during ripening and reduces transportability and shelf life. Disassembly of the cell wall and middle lamella is key in the loss of fruit firmness, and several ripening-associated cell wall-modifying genes have been targeted for genetic modification, particularly pectin modifiers. However, except for pectate lyase, single knockouts of most ripening-associated cell wall genes do not affect cell wall integrity and fruit firmness. The naturally occurring pleiotropic tomato (Solanum lycopersicum) mutants and SlLOB1-repressed fruit show alleviated softening with repression of multiple cell wall genes, indicating that softening is a multigenic trait involving cell wall enzymes that synergistically modify cell wall structure and components.

Question: Does the metabolism of the cellulose–xyloglucan framework affect tomato fruit softening? Do the α-expansin encoded by SlExpansin (SlExp1) and the endoglucanase encoded by SlCellulase2 (SlCel2), which are co-expressed during ripening, cooperate and alter cell wall disassembly during fruit softening?

Findings: The fruit texture and cell wall biochemical changes of single and double mutants showed that simultaneous knockout of SlExp1 and SlCel2 led to considerable inhibition of homogalacturonan (HG)-type pectin and xyloglucan metabolism, smaller intercellular spaces, and firmer fruit. Single knockout of SlExp1 or SlCel2 did not affect fruit firmness, although cell wall biochemical changes were detected in exp1, particularly in HG-type pectin. This result indicates that SlExp1 and SlCel2 synergistically regulate cell wall disassembly and tomato fruit softening. Moreover, modulating SlExp1 and SlCel2 did not alter plant growth and development, fruit taste, or quality-related traits, suggesting a viable approach to enhance fruit texture without sacrificing quality.

Next steps: The mechanism by which SlExp1 and SlCel2 proteins work together must be explored. Furthermore, whether, and to what extent, a synergistic relationship between Exp and Cel contributes to fruit softening in other fleshy fruit species requires further investigation.

 Reference:

Guanqing Su, Yifan Lin, Chunfeng Wang, Jiao Lu, Zimeng Liu, Zhiren He, Xiu Shu, Wenbo Chen, Rongrong Wu, Baijun Li, Changqing Zhu, Jocelyn K. C. Rose, Donald Grierson, James J. Giovannoni, Yanna Shi, Kunsong Chen. (2023). Expansin SlExp1 and endoglucanase SlCel2 synergistically promote fruit softening and cell wall disassembly in tomato. https://doi.org/10.1093/plcell/koad291