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Search indexed bioRxiv preprints in genomics, neuroscience, cell biology and bioinformatics. Read source abstracts and check manuscript versions; preprints are not peer reviewed.

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Widespread Negative Frequency-Dependent Selection Maintains Diversity in the Legume-Rhizobia Symbiosis: Balancing nodulation may explain the paradox of rhizobium diversity

The evolutionary origin and ecological maintenance of biodiversity is a central problem in biology. For diversity to be stable through time, each genotype or species must have an advantage when rare. This negative frequency-dependence prevents deterministic extinction and mitigates the stochastic loss of diversity (1-4). However, models of mutualism typically generate positive frequency-dependence that reduces diversity (5-8). Here, we report empirical evidence for negative frequency-dependence in the legume-rhizobium mutualism within a single host generation, a phenomenon that we term balancing nodulation. Balancing nodulation increases rare rhizobia across all 13 legume genera investigated to date, at high and low inoculum densities, and with minimal genetic differentiation between rhizobia strains. While the mechanism generating this phenomenon is currently unknown, balancing nodulation could actively maintain variation in the rhizobia-legume symbiosis.

plant biology↗

GNOM-Dependent Endosomal Recycling Sets the Timing of Founder Cell Specification

1.Lateral root growth occurs from primed xylem pole pericycle cells that can be specified as founder cells, but how these cells acquire the pluripotency state to initiate a root organogenesis program is not fully understood. Here, we find that the EMS 204 mutant is unable to specify founder cells due to a point mutation affecting the C-terminal HDS3 domain of the GNOM protein. We used genetics and cell biology to study the trafficking machinery of xylem pole pericycle cells, cells in which GNOM is primarily associated with recycling endosomes. We found that the lack of the HDS3 domain negatively affects the stability of the GNOM protein within the cells of the xylem pole pericycle and, subsequently, the integrity of the trafficking machinery of these cells. We determined that GNOM is responsible for the recycling of AUX1 toward the plasma membrane at the xylem pole pericycle and impairment of this recycling results in premature accumulation of AUX1 in the vacuole. In this work, we describe a cell type-specific cellular mechanism and the role of a particular domain during lateral root development.

plant biology↗

Optimized Blue Laser Priming Improves Lettuce Seed Germination and Early Seedling Establishment Under Reduced Water Availability

Continuous-wave (CW) 450 nm blue diode-laser irradiation was evaluated as a physical seed-priming treatment for improving lettuce (Lactuca sativa L.) germination and early seedling establishment under reduced water availability. Dry seeds were irradiated at 50-250 mW for 2 min and at 100 mW for 0.5-10 min; each condition included three independent Petri-dish replicates with 100 seeds per replicate, and the replicates were monitored for 72 h. Laser treatment produced a dose-dependent biological response. The optimized condition, 100 mW for 2 min, increased final germination from approximately 65-70% to 90-95%, increased the germination speed index, and promoted root elongation more strongly than shoot elongation. Longer exposures reduced germination and seedling growth. Under reduced water availability (0.5-6 ml per Petri dish), laser-treated seeds germinated earlier, maintained final germination of 83-93% compared with 57-72% in controls, and produced better-developed seedlings. The relative benefit increased as water availability decreased, indicating that optimized blue laser priming partially compensated for low water supply during germination and early establishment. These results identify CW blue laser priming as a contactless, chemical-free approach for improving lettuce seed performance and early seedling vigor under limited water availability.

plant biology↗

Subnuclear cofactor partitioning underlies auxin-dependent transcriptional regulation

Cellular and organismal function relies on the precise activation and repression of gene expression by DNA-binding transcription factors (TFs). Many TFs occur in large gene families, and a key question in biology is how divergent functions emerge in TF families during evolution. Here we discover the biochemical mechanism for transcriptional activation by the Marchantia polymorpha AUXIN RESPONSE FACTOR1 (MpARF1) TF, which relies on direct recruitment of the Mediator complex into subnuclear MpARF1 clusters. We find that the Mediator recruitment region was the evolutionary innovation that converted ARF repressors into activators, switching binding specificity from co-repressor to co-activator. We demonstrate that this evolutionary innovation can be recreated, thereby revealing a deeply conserved mechanism based on competition between ARF clusters at the heart of the transcriptional auxin response.

plant biology↗

Extracellular NAD(P) activates systemic acquired resistance through LecRK-VI.2-mediated phosphorylation of NPR1

Systemic acquired resistance (SAR) is a long-lasting, broad-spectrum immune response induced in distal tissues by signals generated at primary infection sites. Although numerous mobile immune signals have been implicated in SAR, how these signals are perceived and mechanistically coupled to transcriptional reprogramming in systemic tissues remains poorly understood. Extracellular NAD(P) [eNAD(P)] functions as a key integrative SAR signal that activates immunity through the plasma membrane-localized lectin receptor kinase LecRK-VI.2 and the master immune coactivator NONEXPRESSOR OF PATHOGENESIS-RELATED GENES1 (NPR1). However, the mechanism linking eNAD(P) perception to activation of NPR1 has remained unknown. Here, we show that LecRK-VI.2 constitutively associates with NPR1 and directly phosphorylates NPR1 at T359 and likely S356 upon eNAD(P) perception. NADP+-induced phosphorylation of NPR1 occurs rapidly in vivo and requires LecRK-VI.2. Nonphosphorylatable NPR1 variants abolish eNADP+-induced local and systemic immunity as well as biologically induced SAR, whereas phosphomimetic variants retain NPR1 function. Mechanistically, LecRK-VI.2-mediated phosphorylation promotes NPR1 interaction with TGACG-binding transcription factors (TGAs) and the Mediator subunit MED15, thereby enhancing assembly of a transcriptional activation complex required for defense gene expression. We further demonstrate that NPR1 facilitates TGA-MED15 association in a phosphorylation-dependent manner. Together, these findings establish a receptor-to-coactivator signaling mechanism that directly links extracellular immune signal perception to transcriptional activation. This work closes a major mechanistic gap in the SAR signaling pathway and reveals receptor-mediated coactivator activation as a mechanism for rapid conversion of extracellular immune cues into coordinated transcriptional outputs during systemic immunity.

plant biology↗

Unraveling transcription factor functions through integrative inference of transcriptional networks in Arabidopsis thaliana yields novel regulators involved in reactive oxygen species stress signaling

Gene regulation is a dynamic process in which transcription factors (TFs) play an important role to control spatiotemporal gene expression. While gene regulatory networks describe the interactions between TFs and their target genes, our global knowledge about the complexity of TF control for different genes and biological processes is incomplete. To enhance our global understanding of regulatory interactions in Arabidopsis thaliana, different regulatory input networks capturing complementary information about DNA motifs, open chromatin, TF binding and expression-based regulatory interactions, were combined using a supervised learning approach, resulting in an integrated gene regulatory network (iGRN) covering 1,491 TFs and 31,393 target genes (1.7 million interactions). This iGRN outperforms the different input networks to predict known regulatory interactions and has a similar performance to recover functional interactions compared to state-of-the-art experimental methods like yeast one-hybrid and ChIP-seq. The iGRN correctly inferred known functions for 681 TFs and predicted new gene functions for hundreds of unknown TFs. For regulators predicted to be involved in reactive oxygen species stress regulation, we confirmed in total 75% of TFs with a function in ROS and/or physiological stress responses. This includes 13 novel ROS regulators, previously not connected to any ROS or stress function, that were experimentally validated in our ROS-specific phenotypic assays of loss- or gain-of-function lines. In conclusion, the presented iGRN offers a high-quality starting point to enhance our understanding of gene regulation in plants by integrating different experimental data types at the network level.

plant biology↗

Bark beetle protein elicitors trigger biphasic immune responses in Norway spruce seedlings

Norway spruce (Picea abies) responds to attacks by the spruce bark beetle (Ips typographus) through the rapid activation of local defense mechanisms, but field studies can be difficult to standardize due to variable attack pressure and environmental heterogeneity. Here, we developed a phytotron-based assay that mimics early beetle-associated stress using insect-derived protein extracts, enabling reproducible molecular analyses under controlled conditions. Ten-week-old spruce seedlings were stem-treated with mock buffer or beetle protein extracts, followed by transcriptomic analyses of stem tissues and targeted metabolomic profiling of needles at 2 and 48 h post-inoculation. RT-qPCR analysis revealed rapid transcriptional activation of signaling and defense genes in Norway spruce, with NP-40-based protein extracts producing the most consistent early response. RNA-seq analysis revealed transcriptional dynamics, with 488 differentially expressed genes detected at 2 h and 84 at 48 h post-inoculation relative to mock-treated controls. Early responses at 2 h were characterized by activation of genes associated with immune perception and signal transduction. By 48 h, the response shifted toward accumulation of transcripts encoding defense proteins such as chitinases, defensins, proteinase inhibitors, and pathogenesis-related (PR) proteins. Importantly, a substantial proportion of differentially expressed genes overlapped with those previously identified in mature Norway spruce trees during pioneer bark beetle attack under field conditions, supporting the biological relevance of the assay. In contrast, targeted analyses of secondary metabolites performed in needle tissue revealed limited systemic changes across time points, suggesting that early induced defenses may remain largely localized to the stem. Together, these results demonstrate that beetle-derived proteins trigger a rapid and temporally structured defense response in Norway spruce seedlings and establish a reproducible elicitor-based platform that may provide a broadly applicable framework for investigating bark beetle-induced defenses across conifers. HighlightBark beetle protein elicitors trigger temporally structured immune responses in Norway spruce seedlings that overlap with responses observed in mature trees, with rapid immune signaling at 2 h followed by defense protein accumulation at 48 h.

plant biology↗

Apples before the fall: does shape stability coincide with maturity?

Fruit shape is the result of the interaction between genetic, epigenetic, environmental factors, and stochastic processes. As a core biological descriptor both for taxonomy and horticulture, the point at which shape stability is reached becomes paramount in apple cultivar identification, and authentication in commerce. Twelve apple cultivars were sampled at regular intervals from anthesis to harvest over two growing seasons. Linear and geometric morphometrics were analyzed to establish if and when shape stabilized and whether fruit asymmetry influenced this. Shape stability was detected in seven cultivars, four asymmetric and three symmetric. The remaining five did not stabilize. Shape stability, as defined here, is cultivar-dependent, and when it occurs, it is late in the growing season. Geometric morphometrics detected stability more readily than linear, especially in symmetric cultivars. Key shape features are important in apple marketing, giving the distinctness and apparent uniformity between cultivars expected at point of sale.

plant biology↗

Whole-genome sequence and methylome profiling of the almond (Prunus dulcis D.A.Webb) cultivar Nonpareil

Almond (Prunus dulcis [Mill.] D.A. Webb) is an economically important, specialty nut crop grown almost exclusively in the United States. Breeding and improvement efforts worldwide have led to the development of key, productive cultivars, including Nonpareil, which is the most widely grown almond cultivar. Thus far, genomic resources for this species have been limited, and a whole-genome assembly for Nonpareil is not currently available despite its economic importance and use in almond breeding worldwide. We generated a 615.89X coverage genome sequence using Illumina, PacBio, and optical mapping technologies. Gene prediction revealed 27,487 genes using MinION Oxford nanopore and Illumina RNA sequencing, and genome annotation found that 68% of predicted models are associated with at least one biological function. Further, epigenetic signatures of almond, namely DNA cytosine methylation, have been implicated in a variety of phenotypes including self-compatibility, bud dormancy, and development of non-infectious bud failure. In addition to the genome sequence and annotation, this report also provides the complete methylome of several key almond tissues, including leaf, flower, endocarp, mesocarp, fruit skin, and seed coat. Comparisons between methylation profiles in these tissues revealed differences in genome-wide weighted percent methylation and chromosome-level methylation enrichment. The raw sequencing data are available on NCBI Sequence Read Archive, and the complete genome sequence and annotation files are available on NCBI Genbank. All data can be used without restriction.

plant biology↗

Herbarium genomics reveal signatures of colonization history, lineage turnover, and adaptation during invasion

O_LIA key challenge in invasion biology is dissecting the roles of colonization history, admixture, and selection on invasion success. However, it is often difficult to determine the sources and locations of introduction events as well as the timing and magnitude of gene flow and selection using genomics datasets from contemporary samples. C_LIO_LIWe disentangle the evolutionary processes acting during the North American invasion of Trifolium repens (white clover) using low-coverage whole genome sequencing from 513 herbarium specimens originally collected between 1838-2018. C_LIO_LIIntroduction history paralleled European colonization patterns. The earliest collected samples had predominantly Belgian and British ancestry, with increasing French and Spanish contributions over time in the Mid-Atlantic and South. Genomic diversity increased significantly through time likely driven by admixture between independently introduced lineages. In lowest latitude regions, there is a strong shift in dominant ancestry with limited admixture (i.e., lineage turnover). Putatively adaptive loci exhibited protracted shifts in allele frequency during the invasion, consistent with contemporary clines. C_LIO_LIOur study demonstrates the power of herbarium genomics to provide spatiotemporal insight into recent evolutionary history. We find a complex invasion history that includes multiple introductions, lineage turnover, and admixture that increased genetic diversity and likely facilitated adaptation in this now cosmopolitan plant. C_LI

plant biology↗

Regulatory architecture of disease resistance in maize revealed by multi-omic systems genetics

Complex traits such as disease resistance have been traditionally studied using quantitative genetics. Here, we use systems genetics to integrate disease severity and multi-omic quantitate trait loci (QTL) to uncover biological networks underlying interaction with northern leaf blight (NLB), a yield-limiting disease of corn. Specifically, we integrated transcriptome, (phospho)proteome, and metabolome measurements to map molecular QTL and build predictive regulatory networks following NLB infection. These inferred networks identified a critical signaling module that was genetically validated comprised of a kinase termed NLB SUSCEPTIBLE KINASE 1, a bHLH transcription factor, and the lignin biosynthesis enzyme BROWN MIDRIB 2. Our results demonstrate the feasibility of high-throughput mapping of genetic determinants of gene- product levels and demonstrates the power of systems genetics to identify upstream regulatory genes that confer resistance to NLB that can inform future strategies for crop protection.

plant biology↗

Tree Species as Biomonitors of Air Pollution around a Scrap Metal Recycling Factory in Southwest Nigeria: Implications for Greenbelt Development

Trees are biomonitors and sinks for air pollutants but better sinking ability comes from trees with high tolerance for air pollution. Consequently, this study investigated the Air Pollution Tolerance Index (APTI) and Anticipated Performance Index (API) of six dominant tree species around a scrap metal recycling factory in Ile-Ife, Southwest Nigeria. Biochemical and physiological parameters such as the relative water content, total chlorophyll, leaf extract pH and ascorbic acid content of the leaves of the selected tree species were determined and used to compute the APTI. The biological and socio-economic characters of each tree species were equally examined to determine the API. The APTI of the selected tree species during the dry season was in the N. laevis (11.8) > A. boonei (11.2) > S. siamea (11.0) > B. micrantha (10.8) > T. orientalis (10.6) > T. grandis (9.6). According to the API grading, N. laevis and A. boonei were classified as "good" (62.5% each) tree species for greenbelt development for both dry and wet seasons, while T. orientalis was also classified as a "good" (62.5% each) tree species for greenbelt development for the wet season only. Native tree species such as N. laevis, A. boonei and T. orientalis exhibited better tolerance to gaseous pollutants and are recommended for biomonitoring environmental health and greenbelt establishment.

plant biology↗

Epigenetic silencing of clustered tDNAs in Arabidopsis

Beyond their key role in translation, cytosolic transfer RNAs (tRNAs) are involved in a wide range of other biological processes. Nuclear tRNA genes (tDNAs) are transcribed by the RNA polymerase III (RNAP III) and cis-elements, trans-factors as well as genomic features are known to influence their expression. In Arabidopsis, besides a predominant population of dispersed tDNAs spread along the 5 chromosomes, some clustered tDNAs have been identified. Here, we demonstrate that these tDNA clusters are transcriptionally silent and that pathways involved in the maintenance of DNA methylation play a predominant role in their repression. Moreover, we show that clustered tDNAs exhibit repressive chromatin features whilst their dispersed counterparts contain permissive euchromatic marks. Our data highlight that the combination of both genomic environment and epigenomic landscape contribute to fine tune the differential expression of dispersed versus clustered tDNAs in Arabidopsis.

plant biology↗

Global identification of AGO3-RNA interactions in Chlamydomonas reveals the small RNA-mediated regulation of nuclear and chloroplast gene expression

MicroRNAs (miRNAs) form complexes with Argonaute (AGO) proteins and bind to mRNAs with complementary sequences to repress their expression. Organisms typically possess several hundred miRNAs regulating diverse biological processes. Although the roles of miRNAs have been well elucidated in multicellular organisms, they remain largely unexplored in unicellular organisms. In the green alga Chlamydomonas reinhardtii, the first unicellular organism in which miRNAs were discovered, identifying miRNA target genes remains challenging. Here, we report the high-throughput sequencing of RNA isolated by crosslinking immunoprecipitation (HITS-CLIP) to generate global AGO3-RNA interaction maps, identifying 131 mRNAs derived from nuclear genes. We also detected mRNAs from two chloroplast genes, suggesting that AGO3 may also influence chloroplast gene expression. Our findings indicate that Chlamydomonas small RNAs repress nuclear and chloroplast gene expression. Furthermore, HITS-CLIP analyses are now feasible for any RNA-binding protein in Chlamydomonas, offering new opportunities to uncover the functions of RNA-binding proteins of interest.

plant biology↗

The genetic architecture of recurrent segregation distortion in Arabidopsis thaliana

The equal probability of transmission of alleles from either parent during sexual reproduction is a central tenet of genetics and evolutionary biology. Yet, there are many cases where this rule is violated. Such violations limit intraspecific gene flow and can facilitate the formation of genetic barriers, a first step in speciation. Biased transmission of alleles, or segregation distortion, can result from a number of biological processes including epistatic interactions between incompatible loci, gametic selection, and meiotic drive. Examples of these phenomena have been identified in many species, implying that they are universal, but comprehensive species-wide studies of segregation distortion are lacking. We have performed a species-wide screen for distorted allele frequencies in over 500 segregating populations of Arabidopsis thaliana using reduced-representation genome sequencing. Biased transmission of alleles was evident in up to a quarter of surveyed populations. Most populations exhibited distortion at only one genomic region, with some regions being repeatedly affected in multiple populations. Our results begin to elucidate the species-level architecture of biased transmission of genetic material in A. thaliana, and serve as a springboard for future studies into the basis of intraspecific genetic barriers.

plant biology↗

ARF1 dimerization is essential for vesicle trafficking and dependent on activation by ARF-GEF dimers in Arabidopsis

Membrane traffic maintains the organization of the eukaryotic cell and delivers cargo proteins to their subcellular destinations such as sites of action or degradation. Membrane vesicle formation requires ARF GTPase activation by the SEC7 domain of ARF guanine-nucleotide exchange factors (ARF-GEFs), resulting in the recruitment of coat proteins by GTP-bound ARFs. In vitro exchange assays were done with monomeric proteins, although ARF-GEFs have been shown to form dimers in vivo. This feature is conserved across the eukaryotes, however its biological significance is unknown. Here we demonstrate ARF1 dimerization in vivo and we show that ARF-GEF dimers mediate ARF1 dimer formation. Mutational disruption of ARF1 dimers interfered with ARF1-dependent trafficking but not coat protein recruitment in Arabidopsis. Mutations disrupting simultaneous binding of two ARF1*GDPs by the two SEC7 domains of GNOM ARF-GEF dimer prevented stable interaction of ARF1 with ARF-GEF and thus, efficient ARF1 activation. Our results suggest a model of activation-dependent dimerization of membrane-inserted ARF1*GTP molecules required for coated membrane vesicle formation. Considering the evolutionary conservation of ARFs and ARF-GEFs, this initial regulatory step of membrane trafficking might well occur in eukaryotes in general.

plant biology↗

Dataset-specific thresholds significantly improve detection of low transcribed regulatory genes in polysome profiling experiments

MotivationPolysome profiling is novel, and yet has proved to be an effective approach to detect mRNAs with differential ribosomal load and explore the regulatory mechanisms driving efficient translation. Genes encoding regulatory proteins, having a great influence of the organism, usually reveal moderate to low transcriptional levels, compared, for example, to genes of house-keeping machinery. This complicates the reliable detection of such genes in the presence of technical and/or biological noise. ResultsIn this work we investigate how cleaning of polysome profiling data on Arabidopsis thaliana influences the ability to detect genes with low level of total mRNA, but with a highly differential ribosomal load, i.e. genes translationally active. Suggested data modelling approach to identify a background level of mRNA counts individually for each dataset, shows higher power in detection of low transcribed genes, compared to the use of thresholds for the minimal required mRNA counts or the use of raw data. The significant increase in detected number of regulation-related genes was demonstrated. The described approach is applicable to a wide variety of RNA-seq data. All identified and classified mRNAs with high and low translation status are made available in supplementary material.

plant biology↗

Identification of a role for an E6-like 1 gene in early pollen-stigma interactions in Arabidopsis thaliana

In Arabidopsis, successful pollen-stigma interactions are dependent on rapid recognition of compatible pollen by the stigmatic papillae located on the surface of the pistil and the subsequent regulation of pollen hydration and germination, and followed by the growth of pollen tubes through the stigma surface. Here we have described the function of a novel gene, E6-like 1 (E6L1), that was identified through the analysis of transcriptome datasets, as one of highest-expressed genes in the stigma, and furthermore, its expression was largely restricted to the stigma and trichomes. The first E6 gene was initially identified as a highly-expressed gene during cotton fiber development, and related E6-like predicted proteins are found throughout the Angiosperms. To date, no orthologous genes have been assigned a biological function. Both the Arabidopsis E6L1 and cotton E6 proteins are predicted to be secreted, and this was confirmed using an E6L1:RFP fusion construct. To further investigate E6L1s function, one T-DNA and two independent CRISPR-generated mutants were analyzed for compatible pollen-stigma interactions, and pollen hydration, pollen adhesion and seed set were mildly impaired for the e6l1 mutants. This work identifies E6L1 as a novel stigmatic factor that plays a role during the early post-pollination stages in Arabidopsis.\n\nKey MessageWe describe a function for a novel Arabidopsis gene, E6-like 1 (E6L1), that was identified as a highly-expressed gene in the stigma and plays a role in early post-pollination stages.

plant biology↗