Stages Of Floral Development Research Articles

The effector SJP3 interferes with pistil development by sustaining SHORT VEGETATIVE PHASE 3 expression in jujube.

Jujube witches' broom (JWB) is a phytoplasma disease that causes severe damage to jujube (Ziziphus jujuba) crops worldwide. Diseased jujube plants show enhanced vegetative growth after floral reversion, including leafy flower structures (phyllody) and the fourth whorl converting into a vegetative shoot. In previous research, secreted JWB protein 3 (SJP3) was identified as an inducer of phyllody. However, the molecular mechanisms of SJP3-mediated pistil reversion remain unknown. Here, the effector SJP3 was found to interact with the MADS-box protein SHORT VEGETATIVE PHASE 3 (ZjSVP3). ZjSVP3 was expressed in young leaves and during the initial flower bud differentiation of healthy jujube-bearing shoots but was constitutively expressed in JWB phytoplasma-infected flowers until the later stage of floral development. The SJP3 effector showed the same expression pattern in the diseased buds and promoted ZjSVP3 accumulation in SJP3 transgenic jujube calli. The N-terminal domains of ZjSVP3 contributed to its escape from protein degradation in the presence of SJP3. Heterologous expression of ZjSVP3 in Nicotiana benthamiana produced typical pistil abnormalities, including trichome-enriched style and stemlike structures within the leaflike ovary, which were consistent with those in the mildly malformed lines overexpressing SJP3. Furthermore, ectopic expression of ZjSVP3 directly bound to the zinc finger protein 8 (ZjZFP8) and MADS-box gene SHATTERPROOF 1 (ZjSHP1) promoters to regulate their expression, resulting in abnormal pistil development. Overall, effector SJP3-mediated derepression of ZjSVP3 sustained its expression to interfere with pistil development, providing insight into the mechanisms of pistil reversion caused by JWB phytoplasma in specific perennial woody plant species.

Genome-Wide Identification and Expression Analysis of the COL Gene Family in Hemerocallis citrina Baroni.

Hemerocallis citrina Baroni (H. citrina) is an important specialty vegetable that is not only edible and medicinal but also has ornamental value. However, much remains unknown about the regulatory mechanisms associated with the growth, development, and flowering rhythm of this plant. CO, as a core regulatory factor in the photoperiod pathway, coordinates light and circadian clock inputs to transmit flowering signals. We identified 18 COL genes (HcCOL1-HcCOL18) in the H. citrina cultivar 'Mengzihua' and studied their chromosomal distribution, phylogenetic relationships, gene and protein structures, collinearity, and expression levels in the floral organs at four developmental stages. The results indicate that these genes can be classified into three groups based on phylogenetic analysis. The major expansion of the HcCOL gene family occurred via segmental duplication, and the Ka/Ks ratio indicated that the COL genes of Arabidopsis thaliana, Oryza sativa, Phalaenopsis equestris, and H. citrina were under purifying selection. Many cis-elements, including light response elements, abiotic stress elements, and plant hormone-inducible elements, were distributed in the promoter sequences of the HcCOL genes. Expression analysis of HcCOL genes at four floral developmental stages revealed that most of the HcCOL genes were expressed in floral organs and might be involved in the growth, development, and senescence of the floral organs of H. citrina. This study lays a foundation for the further elucidation of the function of the HcCOL gene in H. citrina and provides a theoretical basis for the molecular design breeding of H. citrina.

Regulated Deficit Irrigation Perspectives for Water Efficiency in Apricot Cultivation: A Review

Addressing agricultural water scarcity poses a current challenge of growing concern, exacerbated by climate change. This is particularly relevant for stone fruit trees, such as apricot, cultivated in semi-arid zones, where regulated deficit irrigation (RDI) strategies are gaining attention to tackle the challenge. The RDI method involves optimizing various factors based on how the plant responds physiologically to indicators of its water needs. Among these indicators, water potential is considered the most reliable and influential measure. For numerous apricot varieties and diverse geographic locations, research consistently shows that implementing water reduction strategies during non-critical developmental stages of floral bud development or fruit growth does not significantly impact crop yield. However, it does lead to reduced vegetative growth, which could offer additional benefits in crop management. Furthermore, the implementation of RDI strategies leads to advantageous improvements in fruit quality, particularly storage capacity and morphometric and chemical fruit characteristics, such as total soluble solids content. This scoping review study suggests that RDI is a feasible strategy to address water scarcity in apricot cultivation; however, further studies focused on continuous water monitoring alternatives are necessary to optimize RDI techniques. Future research should prioritize optimizing RDI for different growth stages, exploring advanced technologies for precise implementation, and assessing environmental impacts, while addressing research gaps including the influence of climate variability and the interaction with other agronomic practices, to refine RDI strategies and enhance apricot orchard sustainability and productivity.

Floral morphology and development of Pteridophyllum racemosum Siebold & Zucc. (Papaveraceae)

ABSTRACT Papaveraceae are known for their often showy flowers and diverse morphologies. Pteridophyllum racemosum (Siebold & Zucc.) is the only member in the Pteridophylloideae within the Papaveraceae, and its phylogenetic position has long been controversial, and a comprehensive analysis of its floral morphology was lacking. Our study focuses on the floral morphogenesis of P. racemosum. Histological sections complemented with scanning electron microscopy allowed a detailed characterization of P. racemosum floral development including description of the vegetative morphology, showing (1) the fine structure of the unusual pinnate leaves; (2) the well-defined floral structure and disymmetry; (3) a series of landmarks in floral development stages, with emphasis on the development of the gynoecium. Interestingly, the P. racemosum floral architecture is similar to that of the proposed ancestral Papaveraceae flower supporting the phylogenetic placement of P. racemosum as an early branching lineage within the Papaveraceae. Our comprehensive overview adds to the colorful library of floral diversity in Papaveraceae, providing a solid base for comparative analyses.

Effect of Warm Temperature Interruption on the Accumulation of Winter Chilling in Kiwifruit (Actinidia chinensis Planch. and A. deliciosa A. Chev.)

Warm temperature exposure during winter has reportedly resulted in the apparent negation of chilling in several fruit species. This study was conducted to investigate the floral and vegetative response of two pistillate kiwifruit cultivars to intermittent warm temperature interruption during chilling accumulation. Dormant 1-year-old canes of Actinidia chinensis ‘AU Golden Dragon’ and Actinidia deliciosa ‘AU Fitzgerald’ were collected in December 2018 and 2019 (334 and 360 chilling units, respectively), shortly after leaf abscission. Canes were cut to 10 nodes after removing the first six basal nodes, placed in jars filled with distilled water, and transferred to respective chilling treatments. Treatments included continuous chilling (CC) (in addition to base chilling) at 1-week (168 chilling units) increments (0–5 weeks) and chilling exposure at the same increments with intermittent warm temperature (WT). For the WT treatments, each week of chilling was followed by 3 days of exposure to warm conditions. Chilling and warm temperature exposure were simulated by 7/4 °C and 25/17.2 °C (day/night) air temperatures, respectively, using separate climate-controlled growth chambers. After treatments, canes were forced in a third chamber at 21.1 to 25.0 °C with light-emitting diode lighting. Vegetative budbreak, floral bud number (from here on defined as floral response), and floral development stage were recorded for each cane at 2-day intervals. For ‘AU Golden Dragon’, WT did not result in any reduced floral response at any of the observed chilling levels. However, lower mean floral response was observed with WT, as compared with CC for ‘AU Fitzgerald’ at 5 weeks of chilling over the 2 years (P = 0.05). WT also lessened the effect of apical dominance with respect to vegetative/floral response to node position for both cultivars. Chilling type had no significant effect on vegetative response in either cultivar. Estimated chilling requirements (CC) in this experiment were similar to those reported previously for these cultivars. Results suggest that A. chinensis cultivars may respond more favorably than A. deliciosa to the erratic winter temperature patterns experienced in the southeastern United States.

Anatomical, histochemical, and developmental approaches reveal the long-term functioning of the floral nectary in Tocoyena formosa (Rubiaceae).

Tocoyena formosa has a persistent floral nectary that continues producing nectar throughout flower and fruit development. This plant also presents an intriguing non-anthetic nectary derived from early-developing floral buds with premature abscised corolla. In this study, we characterize the structure, morphological changes, and functioning of T. formosafloralnectary at different developmental stages. We subdivided the nectary into four categories based on the floral and fruit development stage at which nectar production started: (i) non-anthetic nectary; (ii) anthetic nectary, which follows the regular floral development; (iii) pericarpial nectary, derived from pollinated flowers following fruit development; and (iv) post-anthetic nectary that results from non-pollinated flowers after anthesis. The nectary has a uniseriate epidermis with stomata, nectariferous parenchyma, and vascular bundles, with a predominating phloem at the periphery. The non-anthetic nectary presents immature tissues that release the exudate. The nectary progressively becomes more rigid as the flower and fruit develop. The main nectary changes during flower and fruit development comprised the thickening of the cuticle and epidermal cell walls, formation of cuticular epithelium, and an increase in the abundance of calcium oxalate crystals and phenolic cells near the vascular bundles. Projections of the outer periclinal walls toward the cuticle in the post-anthetic nectary suggest nectar reabsorption. The anatomical changes of the nectary allow it to function for an extended period throughout floral and fruit development. Hence, T. formosa nectary is a bivalent secretory structure that plays a crucial role in the reproductive and defensive interactions of this plant species.

EuAP2a, a key gene that regulates flowering time in peach (Prunus persica) by modulating Thermo-responsive transcription programming

Abstract Frequent spring frost damage threatens temperate fruit production, and the breeding of late-flowering cultivars is an effective strategy for preventing such damage, but the lack of specific genes and markers and a lack of understanding of the mechanisms make it difficult. We examined a Late-Flowering Peach (LFP) germplasm and found that its floral buds require a longer chilling period to release from their dormancy and a longer warming period to bloom than the control cultivar, two key characteristics associated with flowering time. We discovered that a 983-bp deletion in euAP2a, an APETALA2 (AP2)-related gene with known roles in regulating floral organ identity and flowering time, was primarily responsible for late flowering in LFP. This deletion disrupts an miR172 binding site, resulting in a gain-of-function mutation in euAP2a. Transcriptomic analyses revealed that at different stages of floral development, two chilling-responsive modules and four warm-responsive modules, comprising approximately 600 genes, were sequentially activated, forming a unique transcription programming. Furthermore, we found that euAP2a was transiently downregulated during the activation of these thermal-responsive modules at various stages. However, the loss of such transient, stage-specific downregulation of euAP2a caused by the deletion of miR172 binding sites resulted in the deactivation or delay of these modules in the LFP flower buds, suggesting that euAP2a acts as a transcription repressor to control floral developmental pace in peaches by modulating the thermo-responsive transcription programming. The findings shed light on the mechanisms behind late flowering in deciduous fruit trees, which is instrumental for breeding frost-tolerant cultivars.

Flower Initiation Pattern, Developmental Stages, and Seed Morphology of Paraphalaenopsis Labukensis P.S. Shim, A. Lamb & C.L. Chan, An Endangered Orchid in Sabah

Background Paraphalaenopsis labukensis P.S. Shim, A. Lamb & C.L. Chan is a monopodial epiphytic species that can only be found in Sabah. P. labukensis orchids have unique characteristics in that it has a long floral lifespan as compared to other orchid species. The flower developmental pattern of P. labukensis greatly influenced capsule formation and seed maturation. Objective The present research was conducted to record the initiation of flower initiation, and floral morphology, and to observe the flowering and capsule development, as well as the effect of different capsule ages on asymbiotic seed germination. Methods A total of three individual plants of P. labukensis were observed. The flowering stages were characterized by quantitative parameters such as length of inflorescence, diameter, and length of buds, the number of flowers produced, and the length of the capsule formed. All the data were recorded through direct observation. Results Overall, twelve morphological landmark that define each stage of floral development was recorded. Based on the observation, P. labukensis inflorescence was asymmetric and in the shape of a panicle. The number of flowers varied among inflorescences, ranging from 3–5, that blossomed at different times. Furthermore, early capsules appeared 40–90 days after pollination (DAP). Then, 120 DAP of the capsule was selected as the most suitable capsule age for germination as it had reached its maturation period. Conclusion Identifying the duration of the whole flowering developmental process will aid in the production of capsules to attain a reliable and adequate seed source for in vitro seed germination.

Functional analysis of a lily SHORT VEGETATIVE PHASE ortholog in flowering transition and floral development

Lilium is a commercially important genus of bulbous flowers, investigating the flowering molecular mechanisms is important for flowering regulation of lily. MADS-box SHORT VEGETATIVE PHASE (SVP) orthologs are involved in the flowering transition and floral organ differentiation in many plants. In this study, we identified an SVP ortholog from L. × formolongi (LfSVP), which was closely related to Arabidopsis SVP according to phylogenetic analysis. Tissue-specific expression patterns indicated that LfSVP expression levels peaked in the leaves and showed low expression levels in flowering tepals. Stage-dependent expression patterns of LfSVP showed high transcription level in the flowering induction stage under different photoperiods and exhibited transcription peak in the floral budding development stage under long days. Overexpressed LfSVP led to delayed flowering and floral organ defects in Arabidopsis independent of photoperiod. Tobacco rattle virus -induced gene silencing of LfSVP caused a strongly earlier flowering time and floral organ defects of L. × formolongi. Moreover, LfSVP can interact with L. × formolongi APETALA1 (AP1) in both yeast and tobacco cells, and the two may interact to regulate floral organ differentiation. In conclusion, LfSVP is a flowering repressor and may be involved in the regulation of floral organ differentiation. This study will be helpful for the molecular breeding of short-life-period and rich floral patterns lily varieties.

Developmental stages and episode-specific regulatory genes in andromonoecious melon flower development.

Given the lack of specific studies on floral development in melon (Cucumis melo L.), we carried out an extensive study involving morphological and transcriptomic analyses to characterize floral development in this species. Using an andromonoecious line, we analysed the development of floral buds in male and hermaphrodite flowers with both light microscopy and scanning electron microscopy. Based on flower lengths, we established a correlation between the developmental stages and four main episodes of floral development and conducted an extensive RNA sequencing analysis of these episodes. We identified 12 stages of floral development, from the appearance of the floral meristems to anthesis. The main structural differences between male and hermaphrodite flowers appeared between stages 6 and 7; later stages of development leading to the formation of organs and structures in both types of flowers were also described. We analysed the gene expression patterns of the four episodes in flower development to find the genes that were specific to each given episode. Among others, we identified genes that defined the passage from one episode to the next according to the ABCDE model of floral development. This work combines a detailed morphological analysis and a comprehensive transcriptomic study to enable characterization of the structural and molecular mechanisms that determine the floral development of an andromonoecious genotype in melon. Taken together, our results provide a first insight into gene regulation networks in melon floral development that are crucial for flowering and pollen formation, highlighting potential targets for genetic manipulation to improve crop yield of melon in the future.

Small RNA profiling reveals that an ovule-specific microRNA, cja-miR5179, targets a B-class MADS-box gene in Camellia japonica.

The functional specialization of microRNA and its target genes is often an important factor in the establishment of spatiotemporal patterns of gene expression that are essential to plant development and growth. In different plant lineages, understanding the functional conservation and divergence of microRNAs remains to be explored. To identify small regulatory RNAs underlying floral patterning, we performed a tissue-specific profiling of small RNAs in various floral organs from single and double flower varieties (flowers characterized by multiple layers of petals) in Camellia japonica. We identified cja-miR5179, which belongs to a deeply conserved microRNA family that is conserved between angiosperms and basal plants but frequently lost in eudicots. We characterized the molecular function of cja-miR5179 and its target - a B-function MADS-box gene - through gene expression analysis and transient expression assays. We showed that cja-miR5179 is exclusively expressed in ovule tissues at the early stage of floral development. We found that cja-miR5179 targets the coding sequences of a DEFICIENS-like B-class gene (CjDEF) mRNA, which is located in the K motif of the MADS-box domain; and the target sites of miR5179/MADS-box were consistent in Camellia and orchids. Furthermore, through a petal transient-expression assay, we showed that the BASIC PENTACYSTEINE proteins bind to the GA-rich motifs in the cja-miR5179 promoter region and suppresses its expression. We propose that the regulation between miR5179 and a B-class MADS-box gene in C. japonica has a deep evolutionary origin before the separation of monocots and dicots. During floral development of C. japonica, cja-miR5179 is specifically expressed in the ovule, which may be required for the inhibition of CjDEF function. This work highlights the evolutionary conservation as well as functional divergence of small RNAs in floral development.

Hidden from the harsh: Belowground preformation prior to winter determines life history strategy of a temperate perennial herb

In temperate mountains, the belowground organ preformation prior to winter is a well-known adaptation strategy in perennial plants, however its detailed phenology is still poorly understood, particularly with reference to belowground floral morphogenesis. Here we investigate, in detail, the developmental stages occuring belowground and its relation with annual aboveground phenology in a temperate Himalayan herb Trillium govanianum. We studied the species at three selected sites along an altitudinal gradient in Kashmir Himalaya. At each site, we recorded the aboveground phenological stages and also studied periodically the overwintering belowground buds to characterize the various developmental stages. We measured the size of leaf and floral organs in the belowground preformed bud and also at anthesis aboveground to investigate the differences at these two stages. The results reveal that the leaves and flower in T. govanianum are preformed belowground one season prior to aboveground development. The species shows an advanced stage of floral morphogenesis and development during the belowground preformation, including completion of male meiosis and formation of functional ovules. We found no significant difference in the floral organs like anther and ovary length in the belowground bud and aboveground anthesis stages, thereby clearly indicating that these essential floral organs are fully developed in the preformed bud much before the species enters into winter dormancy. Our study suggests that the highly developed floral preformation hidden from the harsh winter conditions plays a pivotal role in the life history strategy of this temperate herb. Overall, our findings advance the current understanding of the belowground phenology, particularly the process of preformation in temperate herbaceous plants.

Floral biology insights into essential oil yield and chemical composition in davana (Artemisia pallens Bess), a high-value aromatic plant of India

Floral organs are identified as the major source of essential oil production in some prime aromatic plants. The quality and quantity of the essential oil are also influenced by the floral developmental stages. The present study was undertaken in A. pallens Bess (davana) with respect to its floral biology and floral sequence in relation to the essential oil yield and its chemical constituents for industrial extraction. The findings revealed that floral (inflorescence) biomass is the primary source of essential oil yield in davana, with the highest oil yield (0.90 ml/100 g) recovered during the blooming stage, followed by herbage (stems and leaves) biomass. Furthermore, cis-davanone, the major chemical constituent of davana essential oil, was recorded at a higher percentage in the bud stage (66.36±0.60%) followed by the blooming stage (60.56±0.20%) and the seed setting stage (40.54±0.80%). These findings can be used to optimize harvest timing in order to obtain higher quality and quantity of davana essential oil.

Comparative transcriptome analysis reveals the involvement of an MYB transcriptional activator, SmMYB108, in anther dehiscence in eggplant.

Male sterility is a highly attractive agronomic trait as it effectively prevents self-fertilization and facilitates the production of high-quality hybrid seeds in plants. Timely release of mature pollen following anther dehiscence is essential for stamen development in flowering plants. Although several theories have been proposed regarding this, the specific mechanism of anther development in eggplant remains elusive. In this study, we selected an R2R3-MYB transcription factor gene, SmMYB108, that encodes a protein localized primarily in the nucleus by comparing the transcriptomics of different floral bud developmental stages of the eggplant fertile line, F142. Quantitative reverse transcription polymerase chain reaction revealed that SmMYB108 was preferentially expressed in flowers, and its expression increased significantly on the day of flowering. Overexpression of SmMYB108 in tobacco caused anther dehiscence. In addition, we found that SmMYB108 primarily functions as a transcriptional activator via C-terminal activation (amino acid 262-317). Yeast one-hybrid and dual-luciferase reporter assays revealed that genes (SmMYB21, SmARF6, and SmARF8) related to anther development targeted the SmMYB108 promoter. Overall, our results provide insights into the molecular mechanisms involved in the regulation of anther development by SmMYB108.

Genome-Wide Identification of the MYB and bHLH Families in Carnations and Expression Analysis at Different Floral Development Stages.

Carnations are one of the most popular ornamental flowers in the world with varied flower colors that have long attracted breeders and consumers alike. The differences in carnation flower color are mainly the result of the accumulation of flavonoid compounds in the petals. Anthocyanins are a type of flavonoid compound that produce richer colors. The expression of anthocyanin biosynthetic genes is mainly regulated by MYB and bHLH transcription factors. However, these TFs have not been comprehensively reported in popular carnation cultivars. Herein, 106 MYB and 125 bHLH genes were identified in the carnation genome. Gene structure and protein motif analyses show that members of the same subgroup have similar exon/intron and motif organization. Phylogenetic analysis combining the MYB and bHLH TFs from Arabidopsis thaliana separates the carnation DcaMYBs and DcabHLHs into 20 subgroups each. Gene expression (RNAseq) and phylogenetic analysis shows that DcaMYB13 in subgroup S4 and DcabHLH125 in subgroup IIIf have similar expression patterns to those of DFR, ANS, and GT/AT, which regulate anthocyanin accumulation, in the coloring of carnations, and in red-flowered and white-flowered carnations, DcaMYB13 and DcabHLH125 are likely the key genes responsible for the formation of red petals in carnations. These results lay a foundation for the study of MYB and bHLH TFs in carnations and provide valuable information for the functional verification of these genes in studies of tissue-specific regulation of anthocyanin biosynthesis.

Genome-wide identification, phylogeny, and expression analysis of GRF transcription factors in pineapple (Ananas comosus).

Pineapple is the only commercially grown fruit crop in the Bromeliaceae family and has significant agricultural, industrial, economic, and ornamental value. GRF (growth-regulating factor) proteins are important transcription factors that have evolved in seed plants (embryophytes). They contain two conserved domains, QLQ (Gln, Leu, Gln) and WRC (Trp, Arg, Cys), and regulate multiple aspects of plant growth and stress response, including floral organ development, leaf growth, and hormone responses. The GRF family has been characterized in a number of plant species, but little is known about this family in pineapple and other bromeliads. We identified eight GRF transcription factor genes in pineapple, and phylogenetic analysis placed them into five subfamilies (I, III, IV, V, VI). Segmental duplication appeared to be the major contributor to expansion of the AcGRF family, and the family has undergone strong purifying selection during evolution. Relative to that of other gene families, the gene structure of the GRF family showed less conservation. Analysis of promoter cis-elements suggested that AcGRF genes are widely involved in plant growth and development. Transcriptome data and qRT-PCR results showed that, with the exception of AcGRF5, the AcGRFs were preferentially expressed in the early stage of floral organ development and AcGRF2 was strongly expressed in ovules. Gibberellin treatment significantly induced AcGRF7/8 expression, suggesting that these two genes may be involved in the molecular regulatory pathway by which gibberellin promotes pineapple fruit expansion. AcGRF proteins appear to play a role in the regulation of floral organ development and the response to gibberellin. The information reported here provides a foundation for further study of the functions of AcGRF genes and the traits they regulate.

Malus Species with Diverse Bloom Times Exhibit Variable Rates of Floral Development

In response to challenges caused by climate change, apple (Malus ×domestica) breeding programs must quickly develop more resilient cultivars. One strategy is to breed for various bloom times. Members of the genus Malus, including domesticated apple, wild species, and hybrids, exhibit striking variations in the bloom date. Although bloom time is strongly influenced by chilling requirements, other aspects of floral development in Malus and their contributions to bloom time are less known. The purpose of this study was to investigate potential connections between predormancy flower development and final bloom time in Malus species. We performed a phenological analysis of flower development in wild and domesticated apple with extreme differences in bloom time over the course of one developmental season. We tracked histological changes in the floral apex of representatives of three early-blooming Malus genotypes (M. ×domestica ‘Anna’ PI 280400, M. orthocarpa PI 589392, M. sylvestris PI 633824) and three late-blooming genotypes (M. angustifolia PI 589763, M. angustifolia PI 613880, M. ×domestica ‘Koningszuur’ PI 188517). Our study documented their floral meristem progression and organ development and expanded on current staging systems for apple flower development to describe the changes observed. The developmental trajectories of each genotype did not group according to bloom category, and we observed variations in the floral development stage at the time of dormancy onset.

Genome-wide identification and analysis of the molecular evolution and expression of type-A response regulator genes in Populus deltoids

Cytokinins have vital effects on various plant development-related processes. Type-A response regulators (RRs) are among the most important regulators in the cytokinin signaling pathway. Specifically, RR genes are the primary cytokinin-responsive genes, encode negative regulators of cytokinin signaling. Similar sex-determining mechanisms involving a type-A RR homolog have recently been identified in sister genera Populus and Salix. Here, we aimed to identify and characterize type-A RR gene family members in Populus deltoides. On the basis of the conserved receiver domain and phylogenetic analysis, we identified 9, 11, and 14 type-A RR genes were identified in P. deltoides, Populus trichocarpa, and Salix suchowensis, respectively. The exon-intron organization and chromosomal locations of these genes in P. deltoides as well as the characteristics of the encoded proteins were analyzed in detail. Gene duplication events, molecular evolution, and phylogenetic relationships were analyzed for all identified type-A RR genes along with 10 Arabidopsis thaliana homologs. These results indicated that the expansion of the type-A RR gene family was primarily due to whole-genome and segmental duplication events. The collinear type-A ARR pairs in A. thaliana were all derived from the α-whole-genome duplication (WGD) event, whereas those in the three Salicaceae species were divided into two groups, one comprising 10 pairs derived from the p-WGD event and the other consisting of 11 pairs derived from the γ-WGD event or a more ancient duplication event. All of the duplicated paralogous gene pairs had undergone purifying selection. Although different type-A RR paralogs experienced different selection pressures, convergent evolution was detected within the receiver domain-encoding sequence, indicative of the importance of this domain for the phosphorelay-related function of the encoded proteins. Three type-A RR genes (PdRR9, PtRR11, and SsRR12) associated with sex determination in Salicaceae species formed a small subclade that lacked A. thaliana counterparts. Evaluation of gene expression in vegetative tissues and at different floral developmental stages in P. deltoides revealed the specific spatiotemporal expression of each PdRR gene, with two (PdRR8 and PdRR9) of the nine PdRR genes exhibiting the opposite sex-biased expression patterns. Diverse expression levels were detected between all eight paralogous PdRR pairs. These findings support future research to elucidate the functional divergence of type-A RR genes.

Heat stress responses vary during floret development in European spring barley cultivars.

The Poaceae, or grasses, include many agriculturally important cereal crops such as rice (Oryza sativa), maize (Zea mays), barley (Hordeum vulgare) and bread wheat (Triticum aestivum). Barley is a widely grown cereal crop used for stock feed, malting and brewing. Abiotic stresses, particularly global warming, are the major causes of crop yield losses by affecting fertility and seed set. However, effects of heat stress on reproductive structures and fertility in barley have not been extensively investigated. In this study we examined three commercial European spring barley varieties under high temperature conditions to investigate the effects on floret development. Using a combination of fertility assays, X-ray micro computed tomography, 3-dimensional modelling, cytology and immunolabelling, we observed that male reproductive organs are severely impacted by increased temperature, while the female reproductive organs are less susceptible. Importantly, the timing of stress relative to reproductive development had a significant impact on fertility in a cultivar-dependent manner, this was most significant at pollen mitosis stage with fertility ranged from 31.6-56.0% depending on cultivar. This work provides insight into how heat stress, when applied during male pollen mother cell meiosis and pollen mitosis, affects barley fertility and seed set, and also describes complementary invasive and non-invasive techniques to investigate floret development. This information will be used to identify and study barley cultivars that are less susceptible to heat stress at specific stages of floral development.

The collaborative mode by PmSVPs and PmDAMs reveals neofunctionalization in the switch of the flower bud development and dormancy for Prunus mume.

Prunus mume (Rosaceae, Prunoideae) serves as an excellent ornamental woody plant with a large-temperature-range cultivation scope. Its flower buds require a certain low temperature to achieve flowering circulation. Thus, it is important to delve into the processes of flower bud differentiation and dormancy, which affected its continuous flowering. These processes are generally considered as regulation by the MADS-box homologs, SHORT VEGETATIVE PHASE (SVP), and DORMANCY-ASSOCIATED MADS-BOX (DAM). However, a precise model on their interdependence and specific function, when acting as a complex in the flower development of P. mume, is needed. Therefore, this study highlighted the integral roles of PmDAMs and PmSVPs in flower organ development and dormancy cycle. The segregation of PmDAMs and PmSVPs in a different cluster suggested distinct functions and neofunctionalization. The expression pattern and yeast two-hybrid assays jointly revealed that eight genes were involved in the floral organ development stages, with PmDAM1 and PmDAM5 specifically related to prolificated flower formation. PmSVP1-2 mingled in the protein complex in bud dormancy stages with PmDAMs. Finally, we proposed the hypothesis that PmSVP1 and PmSVP2 could combine with PmDAM1 to have an effect on flower organogenesis and interact with PmDAM5 and PmDAM6 to regulate flower bud dormancy. These findings could help expand the current molecular mechanism based on MADS-box genes during flower bud development and dormancy.