Expression Of Flowering Genes Research Articles

Widely-targeted metabolomics and transcriptomics identify metabolites associated with flowering regulation of Choy Sum

Choy Sum, a stalk vegetable highly valued in East and Southeast Asia, is characterized by its rich flavor and nutritional profile. Metabolite accumulation is a key factor in Choy Sum stalk development; however, no research has focused on metabolic changes during the development of Choy Sum, especially in shoot tip metabolites, and their effects on growth and flowering. Therefore, in the present study, we used a widely targeted metabolomic approach to analyze metabolites in Choy Sum stalks at the seedling (S1), bolting (S3), and flowering (S5) stages. In total, we identified 493 metabolites in 31 chemical categories across all three developmental stages. We found that the levels of most carbohydrates and amino acids increased during stalk development and peaked at S5. Moreover, the accumulation of amino acids and their metabolites was closely related to G6P, whereas the expression of flowering genes was closely related to the content of T6P, which may promote flowering by upregulating the expressions of BcSOC1, BcAP1, and BcSPL5. The results of this study contribute to our understanding of the relationship between the accumulation of stem tip substances during development and flowering and of the regulatory mechanisms of stalk development in Choy Sum and other related species.

Genome-wide identification and characterization of flowering genes in Citrus sinensis (L.) Osbeck: a comparison among C. Medica L., C. Reticulata Blanco, C. Grandis (L.) Osbeck and C. Clementina

BackgroundFlowering plays an important role in completing the reproductive cycle of plants and obtaining next generation of plants. In case of citrus, it may take more than a year to achieve progeny. Therefore, in order to fasten the breeding processes, the juvenility period needs to be reduced. The juvenility in plants is regulated by set of various flowering genes. The citrus fruit and leaves possess various medicinal properties and are subjected to intensive breeding programs to produce hybrids with improved quality traits. In order to break juvenility in Citrus, it is important to study the role of flowering genes. The present study involved identification of genes regulating flowering in Citrus sinensis L. Osbeck via homology based approach. The structural and functional characterization of these genes would help in targeting genome editing techniques to induce mutations in these genes for producing desirable results.ResultsA total of 43 genes were identified which were located on all the 9 chromosomes of citrus. The in-silico analysis was performed to determine the genetic structure, conserved motifs, cis-regulatory elements (CREs) and phylogenetic relationship of the genes. A total of 10 CREs responsible for flowering were detected in 33 genes and 8 conserved motifs were identified in all the genes. The protein structure, protein-protein interaction network and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis was performed to study the functioning of these genes which revealed the involvement of flowering proteins in circadian rhythm pathways. The gene ontology (GO) and gene function analysis was performed to functionally annotate the genes. The structure of the genes and proteins were also compared among other Citrus species to study the evolutionary relationship among them. The expression study revealed the expression of flowering genes in floral buds and ovaries. The qRT-PCR analysis revealed that the flowering genes were highly expressed in bud stage, fully grown flower and early stage of fruit development.ConclusionsThe findings suggested that the flowering genes were highly conserved in citrus species. The qRT-PCR analysis revealed the tissue specific expression of flowering genes (CsFT, CsCO, CsSOC, CsAP, CsSEP and CsLFY) which would help in easy detection and targeting of genes through various forward and reverse genetic approaches.

Application value of protein phase separation mechanism of flowering regulation in de novo domestication.

Global climate change and population growth pose a serious threat to world food security. The current crops varieties will be insufficient to meet food needs in the future, and there is an urgent need for high yielding and quality crops varieties with strong environmental adaptability. The rapid de novo domestication of wild species to create new germplasm that can be applied to crop breeding is a new strategy for ensuring food security. The flowering time is an important factor in determining the crop planting area and yield, and is a trait that is often selected in crop domestication. At present, the modification of flowering traits by de novo domestication is usually achieved by direct editing of the major genes that control flowering in crop, which are very limited in number and relatively homogeneous in function. Floral transition is regulated by the complex network of environmental and endogenous signals. Here, we propose a new strategy that using genome editing to precisely modify protein function by changing protein phase separation capacity of important proteins that regulate expression of flowering genes, which may provide new options for the design of flowering traits in de novo domestication.

Development of a speed breeding protocol with flowering gene investigation in pepper (Capsicum annuum).

Pepper (Capsicum spp.) is a vegetable and spice crop in the Solanaceae family with many nutritional benefits for human health. During several decades, horticultural traits, including disease resistance, yield, and fruit quality, have been improved through conventional breeding methods. Nevertheless, cultivar development is a time-consuming process because of the long generation time of pepper. Recently, speed breeding has been introduced as a solution for shorting the breeding cycle in long-day or day-neutral field crops, but there have been only a few studies on speed breeding in vegetable crops. In this study, a speed breeding protocol for pepper was developed by controlling the photoperiod and light quality. Under the condition of a low red (R) to far-red (FR) ratio of 0.3 with an extended photoperiod (Epp) of 20h (95 ± 0 DAT), the time to first harvest was shortened by 75 days after transplant (DAT) compared to that of the control treatment (170 ± 2 DAT), suggesting that Epp with FR light is an essential factor for flowering in pepper. In addition, we established the speed breeding system in a greenhouse with a 20h photoperiod and a 3.8 R:FR ratio and promoted the breeding cycle of C. annuum for 110 days from seed to seed. To explain the accelerated flowering response to the Epp and supplemented FR light, genome-wide association study (GWAS) and gene expression analysis were performed. As a result of the GWAS, we identified a new flowering gene locus for pepper and suggested four candidate genes for flowering (APETALA2 (AP2), WUSCHEL-RELATED HOMEOBOX4 (WOX4), FLOWERING LOCUS T (FT), and GIGANTEA (GI)). Through expression analysis with the candidate genes, it appeared that Epp and FR induced flowering by up-regulating the flowering-promoting gene GI and down-regulating FT. The results demonstrate the effect of a combination of Epp and FR light by genetic analysis of flowering gene expression. This is the first study that verifies gene expression patterns associated with the flowering responses of pepper in a speed breeding system. Overall, this study demonstrates that speed breeding can shorten the breeding cycle and accelerate genetic research in pepper through reduced generation time.

LHD3 Encoding a J-Domain Protein Controls Heading Date in Rice

Heading date is one of the most important agronomic traits of rice, which critically affects rice ecogeographical adaptation, yield and quality. In this study, a late heading date 3 (lhd3) mutant was screened from the 60Co-γ irradiation mutant library. The lhd3 delayed heading date in rice under both short day and long day conditions. Map-based cloning combined with Mutmap strategy was adopted to isolate the causal LHD3 gene. The LHD3 gene encodes a DNA_J domain protein, which was ubiquitously expressed in various plant organs, and dominant expressed in stems and leaves. Subcellular localization analysis showed that LHD3 was localized to nucleus, indicating that LHD3 may interact with other elements to regulate the expression of flowering genes. The transcriptions of the heading activators Ehd1, Hd3a and RFT1 significantly decreased in the lhd3 mutant, suggesting that LHD3 may control the heading date through the Ehd1-Hd3a/RFT1 photoperiodic flowering pathway. The variation and haplotype analyses of the genomic region of LHD3 showed that there were 7 haplotypes in the LHD3 region from 4 702 accessions. The haplotypes of LHD3 can be divided into two classes: class a and class b, and the heading dates of these two classes were significantly different. Further study showed that two single nucleotide polymorphisms (SNPs), SNP10 (G2100C) in Hap II and SNP3 (C861T) in Hap VII, may be the functional sites causing early and late heading in accessions. Nucleotide diversity analysis showed LHD3 had been selected in the indica population, rather than in the japonica population. Therefore, the present study sheds light on the regulation of LHD3 on heading date in rice and suggests that LHD3 is a novel promising new target for rice molecular design and breeding improvement.

The Significance of Florigen Activation Complex in Controlling Flowering in Rice

Yield potential, plant height and flowering time are three classes of traits that determine the productivity of rice. Rice heading greatly depends on the accurate measurement of environment changes, particularly in day length and temperature. We discuss all genes reported to be related to the heading time in this review. The accumulation of florigen, such as Hd3a or RFT1, is the key factor for rice heading. Florigen is found in the rice leaf and then transports into the shoot apical meristem (SAM), where floral initiation occurs. We discuss the formation of florigen activation complex (FAC) with 14-3-3 and FD1 proteins to induce the expression of flowering genes. In addition, two key pathways related to heading date, GI-Hd1-Hd3a and Ghd7-Ehd1-Hd3a/RFT1 are introduced in this review. We summarize proteins with histone modification functions, due to the modification of histone is also significant for heading date. The flowering time also extremely dependent on the environments, including nutrient availability, abiotic and biotic stresses, we argue the phenotypes of rice heading date under different extreme environments, as well. Lastly, we gather genes that are reported having a change in heading time, but their detail molecular regulation is still elusive. Thus, this review introduces heading time systematically, providing knowledge and ideas for researchers to study further the phenotype of heading time.

Transcriptome Analysis of the Effects of Grafting Interstocks on Apple Rootstocks and Scions.

Apples are a major horticultural crop worldwide. Grafting techniques are widely utilized in apple production to keep the varieties pure. Interstocks are frequently used in Northern China to achieve intensive apple dwarfing cultivation. High-throughput sequencing was used to investigate differentially expressed genes in the phloem tissues of two different xenograft systems, M ('Gala'/'Mac 9'/Malus baccata (L.) Borkh.) and B ('Gala'/Malus baccata (L.) Borkh.). The results showed that dwarfing interstocks could significantly reduce the height and diameters of apple trees while have few effects on the growth of annual branches. The interstocks were found to regulate the expression of genes related to hormone metabolism and tree body control (GH3.9, PIN1, CKI1, ARP1, GA2ox1 and GA20ox1), these effects may attribute the dwarf characters for apple trees with interstocks. Besides, the interstocks reduce photosynthesis-related genes (MADH-ME4 and GAPC), promote carbon (C) metabolism gene expression (AATP1, GDH and PFK3), promote the expression of nitrogen (N)-metabolism-related genes (NRT2.7, NADH and GDH) in rootstocks, and improve the expression of genes related to secondary metabolism in scions (DX5, FPS1, TPS21 and SRG1). We also concluded that the interstocks acquired early blooming traits due to promotion of the expression of flowering genes in the scion (MOF1, FTIP7, AGL12 and AGL24). This study is a valuable resource regarding the molecular mechanisms of dwarf interstocks' influence on various biological processes and transplantation systems in both scions and rootstocks.

Bacillus velezensis strain B26 modulates the inflorescence and root architecture of Brachypodium distachyon via hormone homeostasis

Plant growth-promoting rhizobacteria (PGPR) influence plant health. However, the genotypic variations in host organisms affect their response to PGPR. To understand the genotypic effect, we screened four diverse B. distachyon genotypes at varying growth stages for their ability to be colonized by B. velezensis strain B26. We reasoned that B26 may have an impact on the phenological growth stages of B. distachyon genotypes. Phenotypic data suggested the role of B26 in increasing the number of awns and root weight in wild type genotypes and overexpressing transgenic lines. Thus, we characterized the expression patterns of flowering pathway genes in inoculated plants and found that strain B26 modulates the transcript abundance of flowering genes. An increased root volume of inoculated plants was estimated by CT-scanning which suggests the role of B26 in altering the root architecture. B26 also modulated plant hormone homeostasis. A differential response was observed in the transcript abundance of auxin and gibberellins biosynthesis genes in inoculated roots. Our results reveal that B. distachyon plant genotype is an essential determinant of whether a PGPR provides benefit or harm to the host and shed new insight into the involvement of B. velezensis in the expression of flowering genes.

Promoting virus-induced gene silencing of pepper genes by a heterologous viral silencing suppressor.

Pepper is an important vegetable cultivated worldwide. Pepper fruits accumulate unique metabolites, capsanthin and capsaicin, which are important raw materials for natural pigment and medicine. Pepper plants are rich in genetic diversity and are attractive subjects for fruit developmental studies. The release of pepper reference genomes provided key genetic information for dissecting function of pepper genes underlying various interesting phenotypes (Kim et al., 2014; Qin et al., 2014). However, due to the difficulty in transformation, dissecting genetic mechanisms in pepper remained technically challenging.

A histone H3K27me3 reader cooperates with a family of PHD finger-containing proteins to regulate flowering time in Arabidopsis.

Trimethylated histone H3 lysine 27 (H3K27me3) is a repressive histone marker that regulates a variety of developmental processes, including those that determine flowering time. However, relatively little is known about the mechanism of how H3K27me3 is recognized to regulate transcription. Here, we identified BAH domain-containing transcriptional regulator 1 (BDT1) as an H3K27me3 reader. BDT1 is responsible for preventing flowering by suppressing the expression of flowering genes. Mutation of the H3K27me3 recognition sites in the BAH domain disrupted the binding of BDT1 to H3K27me3, leading to de-repression of H3K27me3-enriched flowering genes and an early-flowering phenotype. We also found that BDT1 interacts with a family of PHD finger-containing proteins, which we named PHD1-6, and with CPL2, a Pol II carboxyl terminal domain (CTD) phosphatase responsible for transcriptional repression. Pull-down assays showed that the PHD finger-containing proteins can enhance the binding of BDT1 to the H3K27me3 peptide. Mutations in all of the PHD genes caused increased expression of flowering genes and an early-flowering phenotype. This study suggests that the binding of BDT1 to the H3K27me3 peptide, which is enhanced by PHD proteins, is critical for preventing early flowering.

A histone H4 gene prevents drought-induced bolting in Chinese cabbage by attenuating the expression of flowering genes.

Flowering is an important trait in Chinese cabbage, because premature flowering reduces yield and quality of the harvested products. Water deficit, caused by drought or other environmental conditions, induces early flowering. Drought resistance involves global reprogramming of transcription, hormone signaling, and chromatin modification. We show that a histone H4 protein, BrHIS4.A04, physically interacts with a homeodomain protein BrVIN3.1, which was selected during the domestication of late-bolting Chinese cabbage. Over-expression of BrHIS4.A04 resulted in premature flowering under normal growth conditions, but prevented further premature bolting in response to drought. We show that the expression of key abscisic acid (ABA) signaling genes, and also photoperiodic flowering genes was attenuated in BrHIS4.A04-overexpressing (BrHIS4.A04OE) plants under drought conditions. Furthermore, the relative change in H4-acetylation at these gene loci was reduced in BrHIS4.A04OE plants. We suggest that BrHIS4.A04 prevents premature bolting by attenuating the expression of photoperiodic flowering genes under drought conditions, through the ABA signaling pathway. Since BrHIS4.A04OE plants displayed no phenotype related to vegetative or reproductive development under laboratory-induced drought conditions, our findings contribute to the potential fine-tuning of flowering time in crops through genetic engineering without any growth penalty, although more data are necessary under field drought conditions.

Litchi flowering gene expression under temperature effect

Litchi flowering gene expression under temperature effect

Information integration and decision making in flowering time control.

In order to successfully reproduce, plants must sense changes in their environment and flower at the correct time. Many plants utilize day length and vernalization, a mechanism for verifying that winter has occurred, to determine when to flower. Our study used available temperature and day length data from different climates to provide a general understanding how this information processing of environmental signals could have evolved in plants. For climates where temperature fluctuation correlations decayed exponentially, a simple stochastic model characterizing vernalization was able to reconstruct the switch-like behavior of the core flowering regulatory genes. For these and other climates, artificial neural networks were used to predict flowering gene expression patterns. For temperate plants, long-term cold temperature and short-term day length measurements were sufficient to produce robust flowering time decisions from the neural networks. Additionally, evolutionary simulations on neural networks confirmed that the combined signal of temperature and day length achieved the highest fitness relative to neural networks with access to only one of those inputs. We suggest that winter temperature memory is a well-adapted strategy for plants’ detection of seasonal changes, and absolute day length is useful for the subsequent triggering of flowering.

Exploring Heat-Response Mechanisms of MicroRNAs Based on Microarray Data of Rice Post-meiosis Panicle.

To explore heat response mechanisms of mircoRNAs (miRNAs) in rice post-meiosis panicle, microarray analysis was performed on RNA isolated from rice post-meiosis panicles which were treated at 40°C for 0 min, 10 min, 20 min, 60 min, and 2 h. By integrating paired differentially expressed (DE) miRNAs and mRNA expression profiles, we found that the expression levels of 29 DE-miRNA families were negatively correlated to their 178 DE-target genes. Further analysis showed that the majority of miRNAs in 29 DE-miRNA families resisted the heat stress by downregulating their target genes and a time lag existed between expression of miRNAs and their target genes. Then, GO-Slim classification and functional identification of these 178 target genes showed that (1) miRNAs were mainly involved in a series of basic biological processes even under heat conditions; (2) some miRNAs might play important roles in the heat resistance (such as osa-miR164, osa-miR166, osa-miR169, osa-miR319, osa-miR390, osa-miR395, and osa-miR399); (3) osa-miR172 might play important roles in protecting the rice panicle under the heat stress, but osa-miR437, osa-miR418, osa-miR164, miR156, and miR529 might negatively affect rice fertility and panicle flower; and (4) osa-miR414 might inhibit the flowering gene expression by downregulation of LOC_Os 05g51830 to delay the heading of rice. Finally, a heat-induced miRNA-PPI (protein-protein interaction) network was constructed, and three miRNA coregulatory modules were discovered.

Endogenous phytohormones and the expression of flowering genes synergistically induce flowering in loquat

Flowering is an important process for the reproduction of higher plants. Up to this point, the studies on flowering have mostly focused on the model plant Arabidopsis thaliana, and the flowering mechanism of fruit trees remains mostly unknown. The diversity of the flowering time of loquat (Eriobotrya japonica Lindl.) makes it an ideal material to study the regulation of flowering. In this study, we first observed the inflorescence bud differentiation in two varieties of loquat that had different blooming times (cv. Dawuxing (E. japonica), that blooms in the fall and cv. Chunhua (E. japonica×Eriobotrya bengalensis Hook. f.) that blooms in the spring) and found that the starting time of inflorescence bud differentiation and the speed of inflorescence development were responsible for the difference in blooming times. The determination of endogenous phytohormones by high performance liquid chromatography (HPLC) indicated that abscisic acid (ABA), zeatin (ZT), and gibberellin (GA3) promoted flowering in loquat, while indole-3-acetic acid (IAA) was mainly involved in inflorescence bud differentiation in Chunhua. A transcription level analysis illustrated that multiple flowering-related genes could respond to different signals, integrate to the TFL1, AP1 and FT genes, and then synergistically regulate flowering in loquat. Thus, this study provides a new insight into flowering regulation mechanisms in loquat.

Cytokinin accumulation and flowering gene expression are orchestrated for floral meristem development in longan (Dimocarpus longan Lour.) after chemical flower induction

Under non-inductive environmental conditions longan trees (Dimocarpus longan Lour.) were subjected to potassium chlorate (KClO3) applications, solely or in combination with shoot girdling or defoliation treatments, to induce flowering. Treated trees showed visible flower buds four weeks after treatment, while untreated reference trees remained vegetative. Trees treated with KClO3 solely and in combination with apical shoot defoliation flowered terminally at the shoot apex. KClO3 treatment in combination with girdling caused flowering exclusively at the lateral buds immediately below the girdle. Results from histological and hormone analyses are integrated with longan flowering gene expression data to build a comprehensive time course model for chemical flower induction in longan. The increased cytokinin concentration in shoot apex tissues, likely due to de novo biosynthesis and translocation, corresponds with transient up-regulation of the flower promoting gene Dimocarpus longan FLOWERING LOCUS 1 (DlFT1) in mature leaves after KClO3 treatment. Both occur during the presumed period of flower induction approximately at 10 days after treatment. Subsequently, and with some delay floral homeotic genes Dimocarpus longan APETALA 1 (DlAP1) are up-regulated in the buds indicating flower bud development, which coincides with visible floral meristems in histological specimen. The specific cytokinin accumulation and flowering gene expression pattern suggest a tight orchestration of hormonal and genetic pathways in chemically induced longan.

Flowering in Persian walnut: patterns of gene expression during flower development

BackgroundFlower development and sufficient fruit set are important parameters with respect to walnut yield. Knowledge about flowering genes of fruit trees can help to conduct better molecular breeding programs. Therefore, this study was carried out to investigate the expression pattern of some flowering genes (FT, SOC1, CAL, LFY and TFL1) in Persian walnut (cv. Chandler) during the growing season and winter dormancy.ResultsThe results showed that walnut flower induction and initiation in Shahmirzad, Iran occurred in early June and late September, respectively. After meeting chilling and heat requirement, flower differentiation and anthesis occurred in late-March and mid-April to early-May, respectively. Study of flowering gene expression showed that the expression of the FT gene increased in three stages including before breaking of bud dormancy, from late March to late April (coincided with flower differentiation and anthesis) and from late May to mid-June (coincided with flower induction). Like FT, the expression of SOC1 gene increased during flower induction and initiation (mid-May to early-August) as well as flower anthesis (mid-April to early-May). LFY and CAL genes as floral meristem identity genes are activated by FT and SOC1 genes. In contrast with flowering stimulus genes, TFL1 showed overexpression during winter dormancy which prevented flowering.ConclusionThe expression of FT gene activated downstream floral meristem identity genes including SOC1, CAL and LFY which consequently led to release bud dormancy as well as flower anthesis and induction. Also, TFL1 as a flowering inhibitor gene in walnut showed overexpression during the bud dormancy. Chilling accumulation reduced TFL1 gene expression and increased the expression of flowering genes which ultimately led to overcome dormancy.

Flowering gene expression in Indonesian long harvest black rice (Oryza sativa L. ‘Cempo Ireng’)

Many studies have reported the great potency of black rice as functional food for human diet. Cempo Ireng is one of Indonesian black rice cultivars with the highest content of anthocyanin. However, it also suffers from long harvest period. This experiment aims at investigating the behavior of the flowering genes in order to gain basic information to develop this cultivar. We sampled the leaves’ blades of Black Rice ‘Cempo Ireng’ at 48, 55, 68, 81, and 90 DAP then performed RNA isolation and cDNA synthesis, amplification of targeted flowering genes, and a semi-quantitative analysis to see the expression of flowering genes. Our results showed that the flowering genes Hd3a and RFT1 were redundantly up-regulated to induce flowering in black rice Cempo Ireng under a neutral day condition in a tropical region. We also noted that the patterns of FT-like genes and flowering regulatory genes including FT-L5, FT-L6, FT-L9, FT-L10 and Hd1, OsCOL4 were expressed together with two major flowering genes. FT-like genes were temporally co-expressed with two flowering genes Hd3a and RFT1, whereas the Hd1 had a unique expression pattern. Meanwhile, OsCOL4 as the flowering repressor was only detected in the early stage when the flowering gene Hd3a began to express. The results suggest that black rice Cempo Ireng has similar and conserved flowering pathway under a neutral day condition as indicated in the common rice flowering models.

Early and late flowering gene expression patterns in maize

A recommendation of: Maud Irène Tenaillon, Khawla Sedikki, Maeva Mollion, Martine Le Guilloux, Elodie Marchadier, Adrienne Ressayre, Christine Dillmann Transcriptomic response to divergent selection for flowering time in maize reveals convergence and key players of the underlying gene regulatory network https://doi.org/10.1101/461947

Interrelations of growth regulators, carbohydrates and expression of flowering genes (FT, LFY, AP1) in leaf and shoot apex of regular and alternate bearing mango (Mangifera indica L.) cultivars during flowering

Two mango cultivars, Amrapali (regular bearer) and Dashehari (alternate bearer), contrasting for bearing habit was assessed for endogenous phytohormone, carbohydrates and expression of floral inductive genes during flowering. Cultivar Amrapali had higher concentration of growth regulators like ABA, auxin, zeatin, salicylic acid and jasmonic acid and carbohydrates, whereas lower GA content compared to cv. Dashehari and the content increased during flowering when compared to vegetative stage. Gibberellic acid levels was higher in all the stages of bud growth in alternate bearer cv. Dashehari compared to the regular bearer cv. Amrapali. However, the starch content was higher in cv. Amrapali compared to cv. Dashehari. Studies on flower inducing genes indicated that the expression of MiLFY gene was found to be higher in the flowering panicles. Expression of MiFT gene was higher in regular bearer cv. Amrapali compared to the alternate bearer cv. Dashehari and the expression was observed only in leaves which are adjacent to the apical buds during flowering. Higher expression of MiAP1 gene was also observed in the leaves during the floral induction phase. MiFT and MiAP1 genes found to have a negative relation with gibberellic acid and its derivatives. The results indicate that positive regulators of flowering were higher in regular bearing cultivar Amrapali compared to alternate bearing cultivar Dashehari.