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Genetic analysis is important for modern plant molecular biology, and in this regard, the existence of specific mutants is crucial. While genome editing technologies, particularly CRISPR-Cas9, have revolutionized plant molecular biology by enabling precise gene disruption, knockout methods are ineffective for lethal genes, necessitating alternatives like gene knockdown. This study demonstrates the practical generation of a hypomorphic mutant allele, alongside severe null mutant alleles, via the targeting of mRNA splicing sites using CRISPR-Cas9. The Arabidopsis HIGH PLOIDY 2 (HPY2) encodes a yeast NSE2 ortholog, part of the conserved eukaryotic SMC5/6 complex, with SUMO E3 ligase activity essential for cell cycle progression and plant development. Loss-of-function HPY2 mutants exhibit severe dwarfism and seedling lethality, making functional analysis challenging. To overcome these limitations, we created HPY2 knockdown mutants as novel tools to investigate gene function. Of the three mutant alleles, the hpy2-cr1 and hpy2-cr2 mutants resembled the existing severe hpy2-1 allele, both harboring a single base pair insertion in one exon, causing significant root shortening and seedling lethality. In contrast, the hypomorphic mutant hpy2-cr3, which has a five bp deletion at an intron-exon junction, showed relatively longer root growth and survived until the reproductive stage. RT-PCR analysis of hpy2-cr3 revealed atypical mRNAs producing truncated polypeptides that retained some HPY2 function, explaining the milder phenotype. These results establish the successful generation of novel hypomorphic mutant alleles critical for studying the lethal gene HPY2, and demonstrate the usefulness of CRISPR-Cas9 for producing viable hypomorphic mutants for investigating complex genetic interactions. [ABSTRACT FROM AUTHOR]

Soil salinity is a major threat to global agriculture, limiting plant growth and lowering crop yields. Recent advances in CRISPR/Cas9 genome editing technology provide unprecedented precision and efficiency for addressing these challenges by directly modifying the central dogma (CD) of molecular biology in plants. The CD naturally lends itself to tighter multi-level regulation, where transcription and translation are both under control at the same time. A multilayer component of CD such as epigenetic modification, transcription, post-transcriptional modification, translation, and post-translational modification contributes significantly to stress tolerance. Strict control of CD components by Clustered Regularly Interspaced Short Palindromic Repeats, CRISPR-associated protein 9 (CRISPR/Cas9) might lead to the generation of climate smart crops. This review delves into the latest developments in the CRISPR toolbox that improve plant salt tolerance. By targeting key genes involved in transcription and translation, CRISPR/Cas9 makes it easier to modify critical components of the central dogma, allowing plants to better manage salt stress. We explore various CRISPR-based strategies, including base editing, prime editing, transcription regulation, multiplexing, RNA and many more, that reprogram gene expression and protein function to improve salt tolerance. In addition, we discuss how CRISPR can be combined with transcriptional regulation and epigenetic modifications to provide a comprehensive approach to salinity resistance for plants. The review also addresses the issues of off-target effects and efficient delivery systems, recommending novel solutions to improve the precision and applicability of CRISPR technology. This review emphasizes the transformative potential of CRISPR in modifying the central dogma to develop salt-tolerant crops, thereby contributing to sustainable agriculture and global food security. [ABSTRACT FROM AUTHOR]

The Correction Notice in the Journal of Food Measurement & Characterization addresses errors in the reference section of an article on processing healthy crackers for children using sprouted flour mixes. The correction provides complete reference details for several sources related to gluten-free biscuits, finger millet flour, quinoa, and fenugreek seeds. The correction ensures accuracy in the original article's reference section. [Extracted from the article]

Plant crops serve as essential sources of nutritional sustenance, supplying vital nutrients to human diets. However, their productivity and quality are severely jeopardized by factors such as pests, diseases, and adverse abiotic conditions. Addressing these challenges using innovative biotechnological approaches is imperative for advancing sustainable agriculture. In recent years, genome editing technologies have emerged as pivotal genetic tools, revolutionizing plant molecular biology. Among these, the CRISPR–Cas9 system has gained prominence due to its unparalleled precision, streamlined design, and heightened success rates. This review article highlights the profound impact of CRISPR/Cas9 technology on crop improvement. The article critically examines the breakthroughs, ongoing enhancements, and future prospects associated with this cutting-edge technology. In conclusion, the utilization of CRISPR/Cas9 presents a transformative shift in agricultural biotechnology, holding the potential to mitigate longstanding agricultural challenges. [ABSTRACT FROM AUTHOR]

We remember Dr Ajay Parida, a leading plant biotechnologist, whose premature passing has deprived the Indian plant science community of a committed scientist and an able administrator. Born on 12 December 1963 in Bhagabanpur, Cuttack District (now Jajpur district), Odisha, he passed away in Guwahati on 19 July 2022. A collegial scientist, his down-to-earth and approachable nature, as well as his resourcefulness were instrumental in advancing the cause of Indian science and harnessing frontier biotechnological tools as vehicles of social consciousness. His expertise in quantitative DNA variation and molecular marker analysis, paved the way for subsequent research on mangrove molecular diversity at the M. S. Swaminathan Research Foundation (MSSRF), Chennai. His contributions to mangrove biology, genetics and genomics as well as extremophile plant species in the Indian context over two decades are a benchmark in his field. He also provided commendable leadership in his capacity as Director, Institute of Life Sciences (ILS), Bhubaneshwar during the COVID-19 pandemic. [ABSTRACT FROM AUTHOR]

The SABATH gene family is a plant-specific class of small molecule methyltransferases. The first goal of this study was to conduct a genome-wide analysis and in silico characterization of SABATH gene family members in Phaseolus vulgaris. The second goal was to see how the members of the SABATH gene family react to salt and drought stress, as well as their expression patterns when melatonin is added to the mix. Within the scope of the study, 18 Pvul-SABATH proteins were discovered in the Phaseolus vulgaris genome using various in silico methods. These proteins ranged in size from 30.18 to 42.73 kDa and were made up of 268 to 387 amino acids. The Pvul-SABATH proteins had isoelectric points ranging from 4.95 (Pvul-SABATH-8) to 6.08 (Pvul-SABATH-2 and -3). The Pvul-SABATH genes were found to have at least three but no more than four exons. According to the results of the phylogenetic analysis, Pvul-SABATH proteins were found to be clustered in three major groups with Arabidopsis thaliana, Glycine max species, and various methyltransferase members. There was segmental duplication between the Pvul-SABATH-1 and Pvul-SABATH-5 genes, as well as the Pvul-SABATH-10 and Pvul-SABATH-14 genes. By comparing the expression level of Pvul-SABATH genes, their different expression levels depending on the bean cultivars were discovered. Moreover, these findings suggested that Pvul-SABATH genes may play a role in the growth and development process of the plants in response to various biotic and abiotic stresses. The findings of this study, which is the first to look at the SABATH gene family in Phaseolus vulgaris, are thought to be beneficial in plant biotechnology and molecular biology. [ABSTRACT FROM AUTHOR]

MicroRNAs (miRNAs) are small non-coding RNAs which modulate gene expression, promoting the degradation of target mRNAs or altering their translation. In the last decade, the role of miRNAs has been largely investigated, providing interesting evidence about the key role of these molecules in plant cell and molecular biology. Recently, our research team has sequenced the miRNome of Moringa oleifera Lam., a plant species widely used in African ethnobotanical traditions, including food practices and folk medicine. In addition, in the last years, our group has also evaluated the differences between the miRNomes from the M. oleifera leaf and leaf-derived callus, respectively. The present communication reports the study of the miRNA expression profile in M. oleifera young plants grown in vitro under different conditions. In particular, seedlings/young plants cultivated for 2, 15, 30, and 60 days or grown for 30 days and subjected for other 30 days to biotic (i.e., chemical inducer of systemic acquired resistance) and abiotic (i.e., darkness, cold) stressors were analyzed. After nucleic acid extraction and retrotranscription, the level of 19 specific miRNAs was evaluated by qPCR assay. Overall, the amount of all miRNAs was higher in 2-day-old seedlings than in older ones. Cold and biotic stimuli induced the overexpression of more than half of the miRNA set, while darkness triggered downregulation or stabilization of most examined miRNAs. In order to clarify the molecular networks and signalling pathways potentially modulated by moringa miRNAs, the putative mRNA targets of the selected miRNAs were predicted using the psRNATarget bioinformatics approach. This study presents novel and interesting information about the role of specific miRNAs in M. oleifera seedlings during their initial developmental stages, as well as in the presence of simulated environmental stresses. [ABSTRACT FROM AUTHOR]

Chickpea, an important grain legume, suffers from considerable loss of yield due to Fusarium wilt disease. Inaccessibility of resistant gene pool among cultivars and lack of report of resistance, genes from alien sources have been the major constraints for resistance development in this valuable crop. However, along with some other transcription factors, MYB78 was significantly upregulated during chickpea—Fusarium interplay in resistant chickpea genotype. Being a highly recalcitrant species, the transformation of this important crop remained non-reproducible until recently. Following a tissue culture independent plumular meristem transformation protocol, introgression of CaMYB78 TF finally became feasible in chickpea. The overexpressed plants developed resistance against the pathogen but the anthocyanin production in transformed flowers was perturbed. In silico analyses of the anthocyanin biosynthetic key gene promoters reported the occurrence of multiple MYB-binding cis elements. Detailed molecular analyses establish the differential regulatory roles of CaMYB78, resistance response against Foc1 on one hand and suppression of pigmentation during flower development on the other, which is an innovative finding of its kind. [ABSTRACT FROM AUTHOR]

Identification of molecular regulators of hepatocellular carcinoma (HCC) initiation and progression is not well understood. We chemically induced HCC in male Wistar rats by administration of diethyl nitrosamine (DEN) and 2-acetylaminofluorene (2-AFF). Using 2D-electrophoresis and MALDI-TOF–MS/MS analyses, we characterized differentially expressed proteins in liver tissues at early stage of HCC progression. Using RT-PCR analysis, we quantified the mRNA expression of the characterized proteins and validated the transcript expression with tumor tissues of clinically confirmed HCC patients. Using bioinformatic tools, we analyzed a network among the introduced proteins that identified their interacting partners and analyzed the molecular mechanisms associated with signaling pathways during HCC progression. We characterized a protein, namely, pre-mRNA splicing factor 1 homolog (ISY1), which is upregulated at both transcriptome and proteome levels at HCC initiation, progression, and tumor stages. We analyzed the interacting partners of ISY1, namely, APOA-1, SYNE1, MMP10, and MTG1. Real-time PCR analysis confirmed elevated expression of APOA-1 mRNA at HCC initiation, progression, and tumor stages in animals undergoing tumorigenesis. The mRNA expression of the interacting partners was validated with tumor tissues of clinically confirmed liver cancer patients; the analysis revealed significant elevation in expression of transcripts. The transcriptome and proteome analyses complement each other and dysregulation in mRNA and protein expression of these regulators may play critical role in HCC initiation and progression. [ABSTRACT FROM AUTHOR]

Long non-coding RNAs (lncRNAs) have attracted extensive attention due to their important roles in various biological processes, among which lncRNA–protein interaction plays an important regulatory role in plant immunity and life activities. Laboratory methods are time consuming and labor-intensive, so that many computational methods have gradually emerged as auxiliary tools to assist relevant research. However, there are relatively few methods to predict lncRNA–protein interaction of plant. Due to the lack of experimentally verified interactions data, there is an imbalance between known and unknown interaction samples in plant data sets. In this study, a multi-feature fusion method based on linear neighborhood propagation is developed to predict plant unobserved lncRNA–protein interaction pairs through known interaction pairs, called MPLPLNP. The linear neighborhood similarity of the feature space is calculated and the results are predicted by label propagation. Meanwhile, multiple feature training is integrated to better explore the potential interaction information in the data. The experimental results show that the proposed multi-feature fusion method can improve the performance of the model, and is superior to other state-of-the-art approaches. Moreover, the proposed approach has better performance and generalization ability on various plant datasets, which is expected to facilitate the related research of plant molecular biology. [ABSTRACT FROM AUTHOR]

Sequencing technologies are evolving at a rapid pace, enabling the generation of massive amounts of data in multiple dimensions (e.g., genomics, epigenomics, transcriptomic, metabolomics, proteomics, and single-cell omics) in plants. To provide comprehensive insights into the complexity of plant biological systems, it is important to integrate different omics datasets. Although recent advances in computational analytical pipelines have enabled efficient and high-quality exploration and exploitation of single omics data, the integration of multidimensional, heterogenous, and large datasets (i.e., multi-omics) remains a challenge. In this regard, machine learning (ML) offers promising approaches to integrate large datasets and to recognize fine-grained patterns and relationships. Nevertheless, they require rigorous optimizations to process multi-omics-derived datasets. In this review, we discuss the main concepts of machine learning as well as the key challenges and solutions related to the big data derived from plant system biology. We also provide in-depth insight into the principles of data integration using ML, as well as challenges and opportunities in different contexts including multi-omics, single-cell omics, protein function, and protein–protein interaction. Key points: • The key challenges and solutions related to the big data derived from plant system biology have been highlighted. • Different methods of data integration have been discussed. • Challenges and opportunities of the application of machine learning in plant system biology have been highlighted and discussed. [ABSTRACT FROM AUTHOR]

Crop contamination with organic pollutants is an important food safety concern. Since organic pollutants are highly toxic, human consumption of contaminated crops can harm human health. Thus, understanding the mechanisms of how organic pollutants are accumulated in crop plants can aid the development of strategies for safer crop production. It is well known that the Cucurbitaceae family accumulates organic pollutants in its fruits at high concentrations. Previous studies have described the organic pollutant-uptake mechanisms of the Cucurbitaceae family. However, an integrated understanding of organic pollutant uptake by Cucurbitaceae is still lacking. In this review, we discuss the uptake mechanisms from the perspective of plant molecular biology. We clearly show that major latex-like proteins identified from the Cucurbitaceae family play a crucial role in the uptake of organic pollutants. This is the first review to describe the mechanisms underlying the accumulation of organic pollutants in the Cucurbitaceae family across the entire uptake pathway. [ABSTRACT FROM AUTHOR]

A de novo transcriptome analysis was performed in C. album, a temperature sensitive fruit tree in China, after treatment with varied temperatures. A total number of 168,385 transcripts were assembled, comprising of 109,439 unigenes, of which 70,530 were successfully annotated. Compared with control check group (CK), which was treated under 25 °C, the chilling stress (4 °C) treated group (CT), showed about 2810 up-regulated and 2567 down-regulated genes. Whereas, group treated under freezing (− 3 °C) stress (FT) showed an up-regulation and a down-regulation of 1748 and 1459 genes, respectively. GO classification analysis revealed that DEGs related to metabolic processes, single-organism metabolic process, and catalytic activity are significantly enriched in both CT and FT conditions. KEGG pathway enrichment analysis for both CT and FT treatments showed an enrichment of genes encoding or related to glycine/serine and threonine metabolism, alpha-linolenic acid metabolism, carotenoid biosynthesis, photosynthesis-antenna proteins, and circadian rhythm. However, genes related to photosynthesis, carbon fixation in photosynthetic organisms, glutathione metabolism, pyruvate metabolism, nicotinate and nicotinamide metabolism were specifically enriched in CT condition. Nevertheless, FT treatment induced genes related to plant-pathogen interaction, linoleic acid metabolism, plant hormone signal transduction and pentose phosphate pathway. Many of the genes involved in plant hormone signal transduction showed significantly different expression in both FT and CT conditions. However, the change was more evident in FT. Here we present the first of the reports for a de novo transcriptomic analysis in C. album, suggesting that the plant shows differential responses in chilling and freezing temperatures, where the hormone signaling and transduction contribute greatly to FT responses. Our study thus paves way for future research regarding functions of these potentially identified genes. [ABSTRACT FROM AUTHOR]

Most of our current knowledge on plant molecular biology is based on experiments in controlled laboratory environments. However, translating this knowledge from the laboratory to the field is often not straightforward, in part because field growth conditions are very different from laboratory conditions. Here, we test a new experimental design to unravel the molecular wiring of plants and study gene–phenotype relationships directly in the field. We molecularly profiled a set of individual maize plants of the same inbred background grown in the same field and used the resulting data to predict the phenotypes of individual plants and the function of maize genes. We show that the field transcriptomes of individual plants contain as much information on maize gene function as traditional laboratory‐generated transcriptomes of pooled plant samples subject to controlled perturbations. Moreover, we show that field‐generated transcriptome and metabolome data can be used to quantitatively predict individual plant phenotypes. Our results show that profiling individual plants in the field is a promising experimental design that could help narrow the lab‐field gap. SYNOPSIS: A new experimental design based on profiling individual plants of the same inbred line under uncontrolled field conditions produces gene function and phenotype predictions that complement predictions gathered from traditional lab‐based experiments. There is substantial variability in the transcriptomes, metabolomes and phenotypes of individual plants of the same genetic background grown in the same field.This variability can be used to predict gene functions and phenotypes of individual plants.Profiling individual field‐grown plants enables mapping of gene networks and phenotypes, and may help close the lab‐field gap. [ABSTRACT FROM AUTHOR]

The effects of increasing yield and quality of virus-free chewing cane seedlings and their physiological and molecular basis were studied in this study. Results showed that compared with infected seedlings (the control), the yield of chewing cane stems grown from virus-free seedlings increased by 21.81–29.93%, stem length increased by 28.66–34.49 cm, internode length increased by 2.16–2.68 cm, the single stem weight increased by 20.10–27.68%, the reducing sugar increased by 0.91–1.15% (absolute value), and sucrose increased by − 0.06–1.33% (absolute value). The decrease in sucrose content did not reach significant level, but all other parameters were reached significant level. The chlorophyll content, photosynthetic parameters such as stomatal conductance (Gs), net photosynthetic rate (Pn) and transpiration rate (Tr), the activity of photosynthetic key enzymes ribulose-1,5-bisphosphate carboxylase (Rubisco) and phosphoenolpyruvate carboxylase (PEPC), and gene (pepc, rbcS, and rbcL) expression levels were all greater in virus-free seedlings than infected seedlings. The content of superoxide anion (O2−) and malondialdehyde (MDA) in virus-free seedlings was lower than infected seedlings at the main growth stage. With increased development, the activities of the antioxidant enzymes superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT) were gradually higher in virus-free seedlings than infected seedlings. Our results indicate that virus-free seedlings may improve photosynthesis efficiency and promote photosynthesis by increasing chlorophyll content, photosynthetic key enzyme activity, and the gene expression levels in leaves. By increasing the activity of antioxidant enzymes, reducing the degree of membrane lipid peroxidation, and improving the stress resistance of chewing cane, the virus-free chewing cane seedlings increased yield and quality. Our findings provide a scientific and theoretical basis for the promotion and application of virus-free chewing cane seedlings. [ABSTRACT FROM AUTHOR]

We present here a tribute to Satish Chandra Maheshwari (known to many as SCM, or simply Satish), one of the greatest plant biologists of our time. He was born on October 4, 1933, in Agra, Uttar Pradesh, India, and passed away in Jaipur, Rajasthan, India, on June 12, 2019. He is survived by two of his younger sisters (Sushila Narsimhan and Saubhagya Agrawal), a large number of friends and students from around the world. He has not only been the discoverer of pollen haploids in plants but has also contributed immensely to the field of duckweed research and gene regulation. In addition, he has made discoveries in the area of phytochrome research. The scientific community will always remember him as an extremely dedicated teacher and a passionate researcher; and for his wonderful contributions in the field of Plant Biology. See Sopory and Maheshwari (2001) for a perspective on the beginnings of Plant Molecular Biology in India; and see Raghuram (2002a, b) for the growth and contributions of this field in India. [ABSTRACT FROM AUTHOR]

Harvested fruit undergo carbon and energy deprivation. However, the events underlying this energy-related stress in detached fruit and their involvement in cell damage have not yet been elucidated. We showed that supplementing detached sweet oranges with additional carbon or energy sources reduced peel damage, while inhibitors of energy metabolism increased it. We investigated the effect of an exogenous source of carbon (glycerol), energy (ATP), and an inhibitor of energy metabolism 2-deoxy-D-glucose (DeOGlc) + sodium iodoacetate (IAc), on the transcriptome of harvested fruit flavedo (outer peel part). ATP and Gly induced common, but also specific, alternative modes of energy metabolism by reducing the stress caused by energy shortage. They also induced shifts in energy metabolism that led to the production of the intermediates required for plant defense secondary metabolites to form. ATP and Gly triggered changes in the expression of the genes involved in cell lesion containment through a defined pathway involving hormones and redox-mediated signaling. DeOGlc + IAc had a contrasting effect on some of these mechanisms. These chemicals altered the biological processes related to membrane integrity and molecular mechanisms involving reactive oxygen species (ROS) production, and lipid and protein degradation. [ABSTRACT FROM AUTHOR]

Enterocytozoon bieneusi is an opportunistic enteric pathogen which can infect a wide range of animal species and humans. It is the most diagnosed species of Microsporidia in humans and has an impact on public health. Many infected animals including foxes may be a potential source for transmitting E. bieneusi to humans. However, limited information is available on the E. bieneusi prevalence and genotypes in farmed foxes in China. Therefore, in the present study, 344 fresh fecal samples were collected from farmed foxes (Vulpes vulpes and Vulpes lagopus) in Shandong Province, and the prevalence and genotypes of E. bieneusi were examined based on sequence analysis of the ribosomal internal transcribed spacer (ITS) region. The overall E. bieneusi prevalence was 9% (31/344); of them, 6.5% (9/138) in farmed silver foxes (V. vulpes) and 10.7% (22/206) in farmed arctic foxes (V. lagopus). Moreover, four known (Hum-q1, NCF2, HND-1, and Type IV) and two novel E. bieneusi genotypes (SDF1 and SDF2) were identified in farmed foxes in the present study. All of the E. bieneusi genotypes belonged to the zoonotic group based on phylogenetic analysis. In addition, 2, 4, 0, and 11 samples were successfully amplified at MS1, MS3, MS4, and MS7 loci, respectively. The present study reveals E. bieneusi prevalence and genotype distribution in farmed foxes in Shandong Province and enlarged the host and geographic information of E. bieneusi in China. [ABSTRACT FROM AUTHOR]

Alternaria black leaf spot disease of oilseed mustard is a primary cause of yield penalty not only in India but also throughout the world. To assess the degree of tolerance, 47 Indian mustard (Brassica juncea) genotypes were evaluated based on the performance against the causal pathogen Alternaria brassicicola. Genotypes were divided into six tolerance groups including resistant, highly tolerant, moderately tolerant, moderately susceptible, susceptible, and highly susceptible, keeping the nonhost resistant Sinapis alba as resistant control. Genotypes EC399312 and PAB-9511 were found to be the most tolerant. Fourteen morphological traits were evaluated which revealed considerable morphological variability among the genotypes. A number of seeds/siliqua and 1000 seed weight were positively correlated with yield per plant. Insignificant negative correlations had been found among plant height, days to maturity, and disease resistance with yield per plant. Correlation data indicate that seeds/siliqua and siliqua on the main shoot can be highly effective for higher grain yield. Genetic diversity of all genotypes was evaluated using simple sequence repeats (SSR) markers. The genotypes were evaluated for polymorphisms after amplification with 41 SSR primer pairs. Nineteen SSR markers in total were found to be highly informative with a polymorphic information content value > 0.50. The evaluation of genetic similarity and cluster analysis together with disease resistance provides some useful guides for assisting plant breeders in selecting suitable genetically diverse parents for the crossing program as well as for the development of mapping population. [ABSTRACT FROM AUTHOR]

Duckweeds belong to the smallest aquatic flowering plant family, Lemnaceae, and have a rapid doubling time, making this group an excellent system to study reduced morphology and wide environmental adaptability at the molecular level. Despite the availability of genomic and transcriptomic data for duckweed member, Lemna minor, lack of an efficient genetic transformation system has limited its use in plant molecular biology research. The present study reports an efficient and rapid Rhizobium rhizogenes-mediated root transformation system for L. minor. Two different factorial experiments were designed to test the effect of explant type, age, culture media and inoculation methods on transformation efficiency. Leaf and root tip cut explants were inoculated with R. rhizogenes strain MSU 440 harboring pBIN-YFP vector using yellow fluorescent protein (YFP) as a reporter gene for identification of transgenic roots. In addition, two different culture media, full MS and 0.25X Hoagland, and four different infection methods, solid culture, centrifugation, liquid culture and sonication, were compared. After 8 weeks, about 17% of the root tip-cut explants infected via the solid culture method and maintained in 0.25X Hoagland medium had YFP-expressing roots. These transgenic L. minor roots were morphologically similar to normal roots and PCR analysis demonstrated that the YFP-expressing roots were positive for the integration-expected rol genes. The described optimized root transformation procedure is a valuable tool for pursuing high-throughput gene characterization studies in L. minor. [ABSTRACT FROM AUTHOR]

Dendrocalamus hamiltonii is a giant bamboo species native to Indian subcontinent with high economic importance. Nevertheless, highly outcross nature and flowering once in decades impose severe limitation in its propagation. Identification and mixed cultivation of genetically diverse genotypes may assist successful breeding and natural recombination of desirable traits. Characterization of existing genetic diversity and population structure are indispensable for efficient implementation of such strategies, which is facing a major challenge due to non-availability of sequence-based markers for the species. In this study, 8121 EST-SSR markers were mined from D. hamiltonii transcriptome data. Among all, tri-repeats were most represented (52%), with the abundance of CCG/CGG repeat motif. A set of 114 polymorphic markers encompassing epigenetic regulators, transcription factors, cell cycle regulators, signaling, and cell wall biogenesis, detected polymorphism and interaction (in silico) with important genes, that might have role in bamboo growth and development. Genetic diversity and population structure of the three D. hamiltonii populations (72 individuals) revealed moderate to high-level genetic diversity (mean alleles per locus: 5.8; mean PIC: 0.44) using neutral EST-SSR markers. AMOVA analysis suggests maximum diversity (59%) exists within population. High genetic differentiation (Gst = 0.338) and low gene flow (Nm = 0.49) were evident among populations. Further, PCoA, dendrogram, and Bayesian STRUCTURE analysis clustered three populations into two major groups based on geographical separations. In future, SSR marker resources created can be used for systematic breeding and implementation of conservation plans for sustainable utilization of bamboo complex. [ABSTRACT FROM AUTHOR]

Knowledge of genetic relationship among genotypes is an important concern for utilization of germplasm resources in breeding. The need for knowledge in local apple cultivars is increasing and molecular marker analysis has contributed to understanding of the apple genetic diversity and phylogenetic relationship between genotypes. Three different DNA-based techniques, random amplified polymorphic DNA (RAPD), simple sequence repeat (SSR) and amplified fragment length polymorphism (AFLP) were used for detecting genetic variation among the 30 local 'Misket' apple genotypes. A total of 423 bands amplified and 205 polymorphic band were obtained with three marker techniques. Thirty RAPD primers amplified 207 bands, of which 91 were polymorphic (40.1%), 10 SSR primers produced 33 bands and 26 of them were polymorphic (78.78%) and 5 AFLP combinations amplified 183 bands of which 88 were polymorphic (48.08%). The average numbers of polymorphic marker per primer combination were 17.6, 3.03 and 2.6 for AFLP, RAPD and SSR respectively. Our results indicate that SSR was less informative in characterizing closely related 'Misket' apple genotypes, compared with RAPD and AFLP markers. AFLP seemed to best suited for evaluating the genetic relationship among the apple genotypes. Closely related genotypes may require more than one marker technique. The findings will be useful to identify and evaluate the local growing apple genetic resources. [ABSTRACT FROM AUTHOR]

Sophora japonica is a medium-sized deciduous native tree to China. Its flower buds and fruits have special medicinal value. By using 26 highly variable nuclear microsatellites, newly reported here, we assessed the genetic diversity and population structure of 10 representative populations (180 individuals in total) within the species. The results revealed a relatively high genetic diversity in S. japonica (Na = 8.00, He = 0.74, PIC = 0.80, I = 1.67), and reduced genetic variation and heterozygote excess were detected in landrace populations (Na = 5.59, He = 0.71, Ar = 4.11, FIS = − 0.043) when compared with those semi-wild population (Na = 9.7, He = 0.74, Ar = 8.80, FIS = 0.082). A significant bottleneck was detected in two Landraces populations. Moderate differentiation and frequent gene flow were detected among all populations (FST = 0.079, P < 0.05, Nm = 2.893). Mantel test detected a marginal significant pattern of isolation by distance (r = 0.009, P = 0.50), and strong differentiation was observed between most southern and northern populations both by the STRUCTURE clustering and principal coordinate analysis (PCoA), indicating that geographic isolation played a key role in the genetic differentiation of the species. The results from this study will benefit the breeding and conservation of S. japonica, other congener species, and tree species with similar life history traits. [ABSTRACT FROM AUTHOR]

The first issue of Plant Cell Reports was published in August 1981. In 1981 the hot plant biotechnology topics included tissue culture, plant regeneration, protoplasts, horizontal gene transfer, haploid cell production, and biosynthesis of important compounds from cultured plant cells. [Extracted from the article]

The complex 'language' of plant RNA encodes a vast array of biological regulatory elements that orchestrate crucial aspects of plant growth, development and adaptation to environmental stresses. Recent advancements in foundation models (FMs) have demonstrated their unprecedented potential to decipher complex 'language' in biology. In this study, we introduced PlantRNA-FM, a high-performance and interpretable RNA FM specifically designed for plants. PlantRNA-FM was pretrained on an extensive dataset, integrating RNA sequences and RNA structure information from 1,124 distinct plant species. PlantRNA-FM exhibits superior performance in plant-specific downstream tasks. PlantRNA-FM achieves an F1 score of 0.974 for genic region annotation, whereas the current best-performing model achieves 0.639. Our PlantRNA-FM is empowered by our interpretable framework that facilitates the identification of biologically functional RNA sequence and structure motifs, including both RNA secondary and tertiary structure motifs across transcriptomes. Through experimental validations, we revealed translation-associated RNA motifs in plants. Our PlantRNA-FM also highlighted the importance of the position information of these functional RNA motifs in genic regions. Taken together, our PlantRNA-FM facilitates the exploration of functional RNA motifs across the complexity of transcriptomes, empowering plant scientists with capabilities for programming RNA codes in plants., Competing Interests: Competing interestsThe authors declare no competing interests., (© The Author(s) 2024.)

GT-1, which was first identified as a type of plant-specific transcription factor trihelix protein, was initially identified from a nuclear extract of tobacco as a DNA-binding protein that binds to a light-inducible gene promoter. We also constructed a fusion gene between the firefly luciferase gene and the promoter region of I Arabidopsis thaliana MPK3 i gene, which encodes a protein kinase involved in signal transduction of defense responses. 10.1271/bbb.68.803 21 Ono S, Kusama M, Ogura R, Hiratsuka K. Evaluation of the use of the tobacco PR-1a promoter to monitor defense gene expression by the luciferase bioluminescence reporter system. [Extracted from the article]

Main conclusion: This review highlights 50 years of research on the fungal diterpene fusicoccin, during which the molecule went from a tool in plant physiology research to a pharmacological agent in treating animal diseases.Fusicoccin is a phytotoxic glycosylated diterpene produced by the fungus Phomopsis amygdali, a pathogen of almond and peach plants. Widespread interest in this molecule started when it was discovered that it is capable of causing stomate opening in all higher plants, thereby inducing wilting of leaves. Thereafter, FC became, and still is, a tool in plant physiology, due to its ability to influence a number of fundamental processes, which are dependent on the activation of the plasma membrane H+-ATPase. Molecular studies carried out in the last 20 years clarified details of the mechanism of proton pump stimulation, which involves the fusicoccin-mediated irreversible stabilization of the complex between the H+-ATPase and activatory 14-3-3 proteins. More recently, FC has been shown to influence cellular processes involving 14-3-3 binding to client proteins both in plants and animals. In this review, we report the milestones achieved in more than 50 years of research in plants and highlight recent advances in animals that have allowed this diterpene to be used as a 14-3-3 targeted drug. [ABSTRACT FROM AUTHOR]

Key message: The dynamic alterations of the physiological and molecular processes in reproductive stage soybean indicated the dramatic impact caused by drought.Abstract: Drought is a major abiotic stress that limits soybean (Glycine max) production. Most prior studies were focused on either model species or crops that are at their vegetative stages. It is known that the reproductive stage of soybean is more susceptible to drought. Therefore, an understanding on the responsive mechanisms during this stage will not only be important for basic plant physiology, but the knowledge can also be used for crop improvement via either genetic engineering or molecular breeding. In this study, physiological measurements and RNA-Seq analysis were used to dissect the metabolic alterations and molecular responses in the leaves of soybean grown at drought condition. Photosynthesis rate, stomata conductance, transpiration, and water potential were reduced. The activities of SOD and CAT were increased, while the activity of POD stayed unchanged. A total of 2771 annotated genes with at least twofold changes were found to be differentially expressed in the drought-stressed plants in which 1798 genes were upregulated and 973 were downregulated. Via KEGG analysis, these genes were assigned to multiple molecular pathways, including ABA biogenesis, compatible compound accumulation, secondary metabolite synthesis, fatty acid desaturation, plant transcription factors, etc. The large number of differentially expressed genes and the diverse pathways indicated that soybean employs complicated mechanisms to cope with drought. Some of the identified genes and pathways can be used as targets for genetic engineering or molecular breeding to improve drought resistance in soybean. [ABSTRACT FROM AUTHOR]

Plant infection with Agrobacterium rhizogenes leads to the development of a hairy root disease notable for the rapid agravitropic growth of roots on hormone-free nutrient media. In order to look into the interaction of A. rhizogenes with plants and assess opportunities of practical application of hairy root culture, new approaches to their production are elaborated. A method of bacterium-free and plasmid-free production of genetically modified roots (hairy roots) by means of biolistic transformation of leaf explants with a DNA fragment (size of 5461 bp) consisting of genes rolA, rolB, rolC, and rolD are proposed. In most cases, such transformation resulted in the emergence of only adventitious roots with transient expression of rol-genes, and the growth of such roots on hormone-free media ceased in 2-3 months in contrast to genuine hairy roots capable of unrestricted growth. Molecular analysis of different systems of target genes’ expression showed an important role of transgene rolC and host gene of cyclin-dependent protein kinase CDKB1-1 in the maintenance of rapid growth of hairy roots in vitro (in isolated cultures). [ABSTRACT FROM AUTHOR]

Main conclusion A deep bibliometric analysis has been carried out, obtaining valuable parameters that facilitate the understanding around the research in plant using molecular markers. The evolution of the improvement in the field of agronomy is fundamental for its adaptation to the new exigencies that the current world context raises. In addition, within these improvements, this article focuses on those related to the biotechnology sector. More specifically, the use of DNA markers that allow the researcher to know the set of genes associated with a particular quantitative trait or QTL. The use of molecular markers is widely extended, including: restriction fragment length polymorphism, random-amplified polymorphic DNA, amplified fragment length polymorphism, microsatellites, and singlenucleotide polymorphisms. In addition to classical methodology, new approaches based on the next generation sequencing are proving to be fundamental. In this article, a historical review of the molecular markers traditionally used in plants, since its birth and how the new molecular tools facilitate the work of plant breeders is carried out. The evolution of the most studied cultures from the point of view of molecular markers is also reviewed and other parameters whose prior knowledge can facilitate the approach of researchers to this field of research are analyzed. The bibliometric analysis of molecular markers in plants shows that top five countries in this research are: US, China, India, France, and Germany, and from 2013, this research is led by China. On the other hand, the basic research using Arabidopsis is deeper in France and Germany, while other countries focused its efforts in their main crops as the US for wheat or maize, while China and India for wheat and rice. [ABSTRACT FROM AUTHOR]

Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. The author, Dr. Babak Rabiei, was not assigned to its correct affiliation, which is Affiliation 1 to read "Dept. of Crop Production & Genetic Engineering, Faculty of Agricultural Sciences, University of Guilan, P.O. Box: 41,635-1314, Rasht, Iran". B Correction to: Plant Molecular Biology Reporter (2022) 41:164-184 b https://doi.org/10.1007/s11105-022-01346-6 The original version of this article unfortunately contained an error. [Extracted from the article]

I Plant Cell Reports i publishes contributions under the article types: Original full-size research articles Focus articles Reviews Opinion papers Definitions: 1. I Plant Cell Reports i embraces a major trend in biological sciences, introduces a new section to accommodate holistic studies based on -omics data, systems biology, Modern biology progressively moves from reductionist approaches to holistic studies, encompassing whole genomes, transcriptomes, proteomes and metabolomes. In addition to hypothesis-driven mechanistic plant cell and molecular biology studies, and plant biotechnology innovations, I Plant Cell Reports i now introduces a further format for original full-size research articles on plant systems biology/genome-wide studies. [Extracted from the article]

Designing low-phytate crops without affecting the developmental process in plants had led to the identification of ABCC5 gene in soybean. The GmABCC5 gene was identified and a partial gene sequence was cloned from popular Indian soybean genotype Pusa16. Conserved domains and motifs unique to ABC transporters were identified in the 30 homologous sequences retrieved by BLASTP analysis. The homologs were analyzed for their evolutionary relationship and physiochemical properties. Conserved domains, transmembrane architecture and secondary structure of GmABCC5 were predicted with the aid of computational tools. Analysis identified 53 alpha helices and 31 beta strands, predicting 60% residues in alpha conformation. A three-dimensional (3D) model for GmABCC5 was developed based on 5twv.1.B ( Homo sapiens) template homology to gain better insight into its molecular mechanism of transport and sequestration. Spatio-temporal real-time PCR analysis identified mid-to-late seed developmental stages as the time window for the maximum GmABCC5 gene expression, a potential target stage for phytate reduction. Results of this study provide valuable insights into the structural and functional characteristics of GmABCC5, which may be further utilized for the development of nutritionally enriched low-phytate soybean with improved mineral bioavailability. [ABSTRACT FROM AUTHOR]

Salinity is the second most prevalent abiotic stress faced by plants, and rice is not an exception. Through this study, it has been tried upon, to study the relative salinity tolerance of eight local varieties of North East India. Preliminary screening was based on their dose- and time-dependent physiological responses to salinity stress. Among the cultivars, Tampha was found to be relatively more tolerant, whereas MSE9 the most sensitive. To further ascertain their tolerance capacity, MDA and HO content was determined, which also confirmed the tolerance level of the two cultivars. Histochemical assays for root plasma membrane integrity and leaf and root HO and O content also showed more damage in Tampha in comparison to MSE9. Finally, gene expression analysis for Na/K co-transporters, OsHKT2;1, OsHKT2;3 and OsHKT2;4, was performed to observe how the expression level of these transporters varies with the tolerance capacity of these two cultivars in leaves and roots under different time frames. The study reveals Tampha to be the most tolerant and MSE9 the most sensitive when compared to the other six screened cultivars for salinity stress. [ABSTRACT FROM AUTHOR]

Sexual reproduction is achieved by precise interactions between male and female reproductive organs. In plant fertilization, sperm cells are carried to ovules by pollen tubes. Signals from the pistil are involved in elongation and control of the direction of the pollen tube. Genetic, reverse genetic, and cell biological analyses using model plants have identified various factors related to the regulation of pollen tube growth and guidance. In this review, I summarize the mechanisms and molecules controlling pollen tube growth to the ovule, micropylar guidance, reception of the guidance signal in the pollen tube, rupture of the pollen tube to release sperm cells, and cessation of the tube guidance signal. I also briefly introduce various techniques used to analyze pollen tube guidance in vitro. [ABSTRACT FROM AUTHOR]

Main Conclusion: 14-3-3 isoforms were relatively less conserved at the C-terminal region across plant groups. Both Os 14-3-3f and Os 14-3-3g were inducible with differential gene expression levels under different abiotic stress and developmental stages in sensitive and tolerant indica rice cultivars as confirmed both at transcript and protein level. Plant 14-3-3s has been well characterized to function in several signaling pathways, biotic as well as abiotic stress and nutrient metabolism. We attempted comprehensive analysis of 14-3-3 genes in different plant lineages such as green algae ( Chlamydomonas reinhardtii), moss ( Physcomitrella patens) and lycophyte ( Selaginella moellendorffii), dicot Arabidopsis thaliana and monocot Oryza sativa sub sp. japonica at the gene and protein level. Sequence alignment results revealed that 14-3-3 isoforms were evolutionarily conserved across all taxa with variable C-terminal end. Phylogenetic analysis indicated that the majority of 14-3-3 isoforms in rice belong to the non-epsilon group that clustered separately from the dicot group. Segmental duplication event played a significant role in the expansion of both, Arabidopsis and rice, 14-3-3 isoforms as revealed by synteny studies. In silico gene expression using Massive Parallel Signature Sequencing and microarray analysis revealed that 14-3-3 isoforms have variable expression in different tissue types and under different abiotic stress regime in Arabidopsis and japonica rice. Both, semi-quantitative and qPCR results, confirmed that Os14-3-3f and Os14-3-3g were inducible under abiotic stress in lamina and roots of indica rice and relatively higher under salinity and cold stress in Nonabokra, under dehydration stress in N-22 and under exogenous ABA in IR-29 usually after 3-6 h of treatment. Both, 14-3-3f and 14-3-3g, were highly expressed in flag leaves, stems and panicles and mature roots. These results were further confirmed by immunoblot analysis of rice cultivars using Os14-3-3f antibody generated from recombinant Os14-3-3f protein. The results provide the first comprehensive report of Os14-3-3 gene expression in indica rice cultivars which differ in tolerance to abiotic stress that might be useful for further research. [ABSTRACT FROM AUTHOR]

Main conclusion: Aluminum toxicity and sulfate deprivation both regulate microRNA395 expression, repressing its low-affinity sulfate transporter ( SULTR2;1 ) target. Sulfate deprivation also induces the high-affinity sulfate transporter gene ( SULTR12 ), allowing enhanced sulfate uptake. Few studies about the relationships between sulfate, a plant nutrient, and aluminum, a toxic ion, are available; hence, the molecular and physiological processes underpinning this interaction are poorly understood. The Al-sulfate interaction occurs in acidic soils, whereby relatively high concentrations of trivalent toxic aluminum (Al) may hamper root growth, limiting uptake of nutrients, including sulfur (S). On the other side, Al may be detoxified by complexation with sulfate in the acid soil solution as well as in the root-cell vacuoles. In this review, we focus on recent insights into the mechanisms governing plant responses to Al toxicity and its relationship with sulfur nutrition, emphasizing the role of phytohormones, microRNAs, and ion transporters in higher plants. It is known that Al disturbs gene expression and enzymes involved in biosynthesis of S-containing cysteine in root cells. On the other hand, Al may induce ethylene biosynthesis, enhance reactive oxygen species production, alter phytohormone transport, trigger root growth inhibition and promote sulfate uptake under S deficiency. MicroRNA395, regulated by both Al toxicity and sulfate deprivation, represses its low-affinity Sulfate Transporter 2;1 (SULTR2;1) target. In addition, sulfate deprivation induces High Affinity Sulfate Transporters (HAST; SULTR1;2), improving sulfate uptake from low-sulfate soil solutions. Identification of new microRNAs and cloning of their target genes are necessary for a better understanding of the role of molecular regulation of plant resistance to Al stress and sulfate deprivation. [ABSTRACT FROM AUTHOR]

Main conclusion: This review presents genetic and molecular basis of crop height using a rice crop model. Height is controlled by multiple genes with potential to be manipulated through breeding strategies to improve productivity. Height is an important factor affecting crop architecture, apical dominance, biomass, resistance to lodging, tolerance to crowding and mechanical harvesting. The impressive increase in wheat and rice yield during the 'green revolution' benefited from a combination of breeding for high-yielding dwarf varieties together with advances in agricultural mechanization, irrigation and agrochemical/fertilizer use. To maximize yield under irrigation and high fertilizer use, semi-dwarfing is optimal, whereas extreme dwarfing leads to decreased yield. Rice plant height is controlled by genes that lie in a complex regulatory network, mainly involved in the biosynthesis or signal transduction of phytohormones such as gibberellins, brassinosteroids and strigolactones. Additional dwarfing genes have been discovered that are involved in other pathways, some of which are uncharacterized. This review discusses our current understanding of the regulation of plant height using rice as a well-characterized model and highlights some of the most promising research that could lead to the development of new, high-yielding varieties. This knowledge underpins future work towards the genetic improvement of plant height in rice and other crops. [ABSTRACT FROM AUTHOR]

A comprehensive study on characterization and genetic diversity analysis was carried out in 16 'Ogura'-based 'CMS' lines of cabbage using 14 agro-morphological traits and 29 SSR markers. Agro-morphological characterization depicted considerable variations for different horticultural traits studied. The genotype, ZHA-2, performed better for most of the economically important quantitative traits. Further, gross head weight (0.76), head length (0.60) and head width (0.83) revealed significant positive correlation with net head weight. Dendrogram based on 10 quantitative traits exhibited considerable diversity among different CMS lines and principle component analysis (PCA) indicated that net and gross head weight, and head length and width are the main components of divergence between 16 CMS lines of cabbage. In molecular study, a total of 58 alleles were amplified by 29 SSR primers, averaging to 2.0 alleles in each locus. High mean values of Shannon's Information index (0.62), expected (0.45) and observed (0.32) heterozygosity and polymorphic information content (0.35) depicted substantial polymorphism. Dendrogram based on Jaccard's similarity coefficient constructed two major groups and eight sub-groups, which revealed substantial diversity among different CMS lines. In overall, based on agro-morphological and molecular studies genotype RRMA, ZHA-2 and RCA were found most divergent. Hence, they have immense potential in future breeding programs for the high-yielding hybrid development in cabbage. [ABSTRACT FROM AUTHOR]

Papaya leaf curl disease (PaLCuD) caused by papaya leaf curl virus (PaLCuV) not only affects yield but also plant growth and fruit size and quality of papaya and is one of the most damaging and economically important disease. Management of PaLCuV is a challenging task due to diversity of viral strains, the alternate hosts, and the genomic complexities of the viruses. Several management strategies currently used by plant virologists to broadly control or eliminate the viruses have been discussed. In the absence of such strategies in the case of PaLCuV at present, the few available options to control the disease include methods like removal of affected plants from the field, insecticide treatments against the insect vector ( Bemisia tabaci), and gene-specific control through transgenic constructs. This review presents the current understanding of papaya leaf curl disease, genomic components including satellite DNA associated with the virus, wide host and vector range, and management of the disease and suggests possible generic resistance strategies. [ABSTRACT FROM AUTHOR]

Key message: Analysis of 387 sugarcane clones using Bru 1 diagnostic markers revealed two possible sources of Bru 1 in Chinese cultivars: one from Saccharum spontaneum and another from Saccharum robustum of New Guinea. Abstract: Sugarcane brown rust (SBR) is an important fungal disease in many sugarcane production areas around the world, and can cause considerable yield losses in susceptible sugarcane cultivars. One major SBR resistance gene, named Bru1, initially identified from cultivar R570, was shown to be a major SBR resistance source in most of the sugarcane producing areas of the world. In this study, by using the two Bru1-associated markers, R12H16 and 9O20-F4, we surveyed the presence of Bru1 in a Chinese sugarcane germplasm collection of 387 clones, consisting of 228 hybrid cultivars bred by different Chinese sugarcane breeding establishments, 54 exotic hybrid cultivars introduced from other countries and 105 clones of sugarcane ancestral species. The Bru1-bearing haplotype was detected in 43.4% of Chinese sugarcane cultivars, 20.4% of exotic hybrid cultivars, and only 3.8% of ancestral species. Among the 33 Chinese cultivars for which phenotypes of resistance to SBR were available, Bru1 was present in 69.2% (18/26) of the resistant clones. Analyses of the allelic sequence variations of R12H16 and 9O20-F4 suggested two possible sources of Bru1 in Chinese cultivars: one from S. spontaneum and another from S. robustum of New Guinea. In addition, we developed an improved Bru1 diagnostic marker, 9O20-F4- HaeIII, which can eliminate all the false results of 9O20-F4- RsaI observed among S. spontaneum, as well as a new dominant Bru1 diagnostic marker, R12E03-2, from the BAC ShCIR12E03. Our results provide valuable information for further efforts of breeding SBR-resistant varieties, searching new SBR resistance sources and cloning of Bru1 in sugarcane. [ABSTRACT FROM AUTHOR]

Molecular studies indicate that Penaeaceae, Oliniaceae, and the monospecific families Alzateaceae and Rhynchocalycaceae form a clade of Myrtales. Of these four families, Penaeaceae have tracheids with vestured pits, whereas the others have septate fibers lacking vestures; all have vestured pits in vessels. Tracheid presence in Penaeaceae may be related to the arid South African habitats of the family. Presence of vestures on tracheids in families with vestured vessel pits is one indication that imperforate elements are tracheids and are conductive cells, whereas fiber-tracheids and libriform fibers are non-conductive. Tracheids occur widely in angiosperms and may be plesiomorphies or apomorphies. Combretaceae, the first branch of the Myrtales clade, has a great diversity of vesture features in vessels compared to the Penaeaceae alliance families. Alzatea has vestures that spread over the inside of the vessels, whereas in most taxa of the alliance, vestures are confined to the pit cavities and pit apertures. Vestures in the alliance tend to be globular in shape, and are bridged together by strands of wall material. Lignotubers and roots in Penaeaceae have vestures much like those in stems. Only a few species and genera (notably Alzatea) of the alliance have vesture features the pattern of which correlates with the current taxonomic system. Vestured pits should be viewed from the inside surface of vessels as well as the outer surface, and although sectional views of vestured pits are infrequent, they are very informative. Studies that explore diversity from one order or family to another are needed and offer opportunities for understanding the evolutionary significance of this feature. [ABSTRACT FROM AUTHOR]

Taxonomic and molecular phylogenetic investigation of the genus Prangos with special attention to the species from subsections Koelzella and Fedtschenkoana, distributed in mountainous South-west Asia and Middle Asia, has been carried out. Morphological and carpological features as well as sequences of nrITS/ETS show that Prangos and relative genera Cachrys and Bilacunaria are monophyletic taxa. The phylogenetic results of the current study do not agree with any published infrageneric classifications of Prangos. The majority of intrageneric taxa of Prangos turn out as non-monophyletic groups. Such taxonomically believed morphological features of Prangos as the architecture of inner mesocarp of the fruit are more labile than previously thought. The most important character of the fruit surface is the presence or absence of stomata. The subsection Koelzella comprises two lineages, one of which includes a representative of subsection Fedtschenkoana. The first lineage, designed as ' Prangos pabularia' clade, includes the Middle Asian species, except for P. equisetoides, segregated as new subgenus Koelzella. The second lineages, designed as ' Prangos uloptera' clade, include P. uloptera, P. lophoptera, and P. equisetoides and remained in new section Ulopterae of subgenus Prangos. Independent taxonomic statuses of P. tschimganica, P. lipskyi, P. ornata, P. equisetoides from P. uloptera, and P. fedtschenkoi and P. lophoptera from P. pabularia are confirmed. Prangos gyrocarpa and P. seravschanica were recognized as the subspecies of P. pabularia: subsp. gyrocarpa and subsp. sarawschanica, respectively. [ABSTRACT FROM AUTHOR]

The aim of the study is to compare distinct morphological characters of Metrodorea (Rutaceae) with those of related genera, under a phylogenetic approach. Morphoanatomy of leaves was analyzed, and data concerning reproductive structures were compiled from the literature. We used available molecular sequences to recover a maximum likelihood tree, and we present a reconstruction of ancestral morphological character states made with the maximum likelihood criterion. The topologies obtained retrieve as synapomorphic characters of Metrodorea: aborted leaflets, vascularized intrapetiolar stipules, sinuous cell walls contour in the surface view of the epidermis, glandular trichomes on the adaxial and proximal region of the petiole, good development of areoles, muricate fruits, and valvate estivation of the corolla. The specific relationships within Metrodorea and between Metrodorea and other genera of Rutoideae are supported by characters as the location of crystals, type of adherence at leaf bases, and presence/absence of trichomes on the blade. The close relationship of Metrodorea and Raulinoa is strongly supported by several synapomorphies. Our data are mostly consistent with recent phylogenies, showing that the monophyly of Esenbeckia cannot be confirmed and that the clade Helietta- Balfourodendron (formerly included in another subfamily) is closely related to Raulinoa and Metrodorea (both part of Pilocarpinae) than to Pilocarpus itself. Possible relationships between these genera are discussed based on the morphological states found, and most of them supporting the hypothesis that Metrodorea is the sister group of Raulinoa. [ABSTRACT FROM AUTHOR]

The pre-germinative metabolism is among the most fascinating aspects of seed biology. The early seed germination phase, or pre-germination, is characterized by rapid water uptake (imbibition), which directs a series of dynamic biochemical events. Among those are enzyme activation, DNA damage and repair, and use of reserve storage compounds, such as lipids, carbohydrates and proteins. Industrial seedling production and intensive agricultural production systems require seed stocks with high rate of synchronized germination and low dormancy. Consequently, seed dormancy, a quantitative trait related to the activation of the pre-germinative metabolism, is probably the most studied seed trait in model species and crops. Single omics, systems biology, QTLs and GWAS mapping approaches have unveiled a list of molecules and regulatory mechanisms acting at transcriptional, post-transcriptional and post-translational levels. Most of the identified candidate genes encode for regulatory proteins targeting ROS, phytohormone and primary metabolisms, corroborating the data obtained from simple molecular biology approaches. Emerging evidences show that epigenetic regulation plays a crucial role in the regulation of these mentioned processes, constituting a still unexploited strategy to modulate seed traits. The present review will provide an up-date of the current knowledge on seed pre-germinative metabolism, gathering the most relevant results from physiological, genetics, and omics studies conducted in model and crop plants. The effects exerted by the biotic and abiotic stresses and priming are also addressed. The possible implications derived from the modulation of pre-germinative metabolism will be discussed from the point of view of seed quality and technology. [ABSTRACT FROM AUTHOR]

In comparison with other Macaronesian Islands (e.g., the Canary Islands), the Cape Verde Islands have received little attention in terms of plant molecular phylogenetic studies, which might also elucidate the general floristic history of this archipelago. The Cape Verdean vascular plant flora (ca. 12% endemics) has traditionally been regarded as relict of a former subtropical Tertiary flora. In contrast, it has been postulated more recently that the flora is much younger and of Pleistocene origin. To test these hypotheses, we have produced molecular phylogenies associated with a molecular clock approach, sampling all nine Cape Verdean endemic Diplotaxis taxa and 21 accessions representing the D. harra complex from across its distributional range. Analyzing three molecular markers from the nuclear and chloroplast genome, we provide evidence that the Cape Verdean endemic Diplotaxis originated from North African D. harra populations in Pleistocene times, putatively linked to the genesis of the (western) Sahara. This adds to the emerging picture that the present Cape Verdean flora is of Pleistocene origin. [ABSTRACT FROM AUTHOR]

Relationships among numerous specimens of Drepanocladus angustifolius (35 specimens), Drepanocladus lycopodioides (71 specimens), and Drepanocladus turgescens (102 specimens) are analysed based on the nuclear internal transcribed spacers 1 and 2 (ITS) and a portion of glyceraldehyde 3-phosphate dehydrogenase ( gpd), and the plastid rpl16 G2 intron. Molecular data suggest that neither species is monophyletic as well as significant incongruence among molecular markers. No statistical support for recombination (ITS, gpd) was found. For some D. lycopodioides and D. turgescens specimens, the molecular information even suggests that they belong to the wrong one of these two species. All such specimens were collected in south Swedish areas where the two species are frequently found growing together and where sporophytes are often common. The occurrence of all such specimens only in these geographical areas is statistically unlikely and suggests that hybridisation occasionally occurs here. While molecular information suggests that the species are not monophyletic, geographical signals could be found for both D. angustifolius and D. turgescens. [ABSTRACT FROM AUTHOR]