Journal of Plant Research最新文献

Breeders adjust wheat heading dates to improve regional adaptability and reduce or mitigate yield losses caused by meteorological disasters, pests and diseases. The Ppd-1 genes play a crucial role in determining wheat sensitivity to changes in day-length and serve as key regulators of heading dates once the vernalization requirement is satisfied. In this study, we identified a new allelic variant of the promoter region, Ppd-B1a.3, in the Chinese wheat cultivar Qingchun 37. Compared to the Ppd-B1b.1 (carried by Chihokukomugi), the main mutation sites in Ppd-B1a.3 include a substitution of C with G at the -505-bp, a T base insertion at the -625-bp, a mutation of TCG to GGT at the -632 to -634-bp, and a 163-bp insertion at the -691 bp. Analysis of F₂ populations indicated that Ppd-B1a.3 promotes heading and flowering (approximately 6 days earlier in population 1 and 17 days in population 2) under short-day conditions in a greenhouse. However, the evaluation of Ppd-B1a.3's effect under field conditions may be influenced by the copy number of the Ppd-B1 locus inherited from the other parent in the F₂ populations. Ppd-B1a.3 disrupts circadian rhythm expression and exhibits a stronger effect on heading and flowering than the three-copy Ppd-B1 allele carried by Jing 411. Origin analysis suggests that Ppd-B1a.3 may have derived from non-native germplasm. These results deepen our understanding of wheat photoperiod genes and provide useful genetic resources for fine-tuning wheat heading dates during breeding.

Thiol/disulfide-based redox regulation is a key mechanism for modulating protein functions in response to changes in cellular redox status. Two thioredoxin (Trx)-like proteins [atypical Cys His-rich Trx (ACHT) and Trx-like2 (TrxL2)] have been identified as crucial for oxidizing and deactivating several chloroplast enzymes during light-to-dark transitions; however, their roles remain to be fully understood. In this study, we investigated the functions of Trx-like proteins in seed development. Using the CRISPR/Cas9 system, we generated an Arabidopsis quadruple mutant defective in ACHT1, ACHT2, TrxL2.1, and TrxL2.2 (acht/trxl2). This mutant showed increased seed lethality prior to maturation, with embryogenesis impaired primarily during the heart and torpedo stages, which are critical phases for plastid differentiation into chloroplasts. Using transgenic plants expressing EGFP-fused proteins, we confirmed that ACHT and TrxL2 are localized in plastids during embryogenesis. Additionally, seed development in the acht/trxl2 mutant was further impaired under extended darkness and could not be recovered through complementation with variants of ACHT or TrxL2 lacking the redox-active Cys residue (replaced by Ser). These findings indicate that the protein-oxidation functions of ACHT and TrxL2 are important for plastid differentiation into chloroplasts, embryogenesis, and seed development.

Analysis of the sex expression in 10 'Lemon' (mmff) cucumber plants (Cucumis sativus L.), known to be andromonoecious, revealed that 3 plants produced female flowers with short ovaries, resembling bisexual flowers, after producing male and bisexual flowers. To investigate the heredity pattern governing these aberrant female flowers with short ovaries, F₁ hybrid plants (MmFf) were generated through a cross between 'Dokanari-sennari' (MMFF) and 'Lemon' (mmff), and #4 (mmff) and #45 (mmFF) were meticulously selected from a pool of 45 F₂ segregants. Analysis of the sex expression in both 10 F₅ plants (mmff) derived from the #4 (mmff) and 10 F₄ plants (mmFF) derived from the #45 (mmFF) revealed that 8-9 plants produced female flowers with short ovaries after producing male and bisexual flowers. Notably, no female flowers with short ovaries were produced in the plants carrying the M gene, such as 'Dokanari-sennari' (MMFF), 8 F₁ hybrid plants (MmFf), and the 29 F₂ segregants (M-F-,M-ff). Thus, female flowers with short ovaries may be produced in some 'Lemon' (mmff) cucumber plants and their progeny, particularly those carrying the mm genotype (CS-ACS2 genes with c.97G > T mutations), after the production of male and bisexual flowers. However, no clear genetic rules governing the occurrence of these female flowers with short ovaries were observed. This is the first report on trimonoecious cucumber plants displaying male flowers, bisexual flowers with short ovaries, and female flowers with short ovaries, all on the same plant, under the influence of the mm genotype (CS-ACS2 genes with c.97G > T mutations).

Plants defend themselves against herbivores by recognizing herbivore-derived elicitors and activating intracellular signaling. In Arabidopsis, the receptor-like kinase HAK1 recognizes the poly-saccharide elicitor (FrA) from Spodoptera litura larvae, leading to the expression of defense-related genes such as PDF1.2. During this process, the cytoplasmic kinase CRK2 phosphorylates PBL27, triggers the ERF13 expression via ethylene signaling and subsequently leads to PDF1.2 expression. Herein, we investigated four cytoplasmic kinases from the same receptor-like cytoplasmic kinase (RLCK) VII family as PBL27 that interacts with CRK2. Among them, PBL11, like PBL27, is phosphorylated by CRK2 and induces PDF1.2 expression but does not affect ERF13 expression. The weight gain of S. litura larvae on PBL11-deficient mutant plants was only slightly higher than that of wild-type plants, suggesting that PBL11 may function as a minor RLCK that supports the defense response.

In the Malveae tribe (Malvaceae), the axis supporting the flower has a joint at the upper third. This axis can be considered as an articulated pedicel, peduncle, peduncle-pedicel, or anthopodium. Such disparity in terminology reveals a duality in interpretation since this structure is classified as part of the inflorescence or part of the flower. In an effort to reach a consensus, this study aims to evaluate axes supporting the flowers of species from the Malveae tribe through ontogenetic, morphological, and histochemical analyses, using light microscopy and scanning electron microscopy. Ontogenetic analyses indicated that the axis supporting the flower is an articulated pedicel, which is divided into proximal and distal parts owing to the presence of the constriction (joint). Simultaneously, the articulated pedicel arises from the floral meristem, along with the establishment of the calyx and androecium. As development progresses, we observed frequent abscissions of the floral bud, along with the distal portion of the pedicel, at the joint. After this, the remaining proximal portion of the pedicel becomes secretory, as an extrafloral nectary, often foraged by ants of the genus Wasmannia. Thus, this ontogenetic analysis of the articulated pedicel helps in understanding its functionality and morphological variability, highlighting the importance of standardized terminology since it would lead to conceptual clarity in different studies. Additionally, this study, for the first time, reveals the presence of extrafloral nectaries on articulated pedicels in Malveae, a previously undocumented feature in Malveae and Malvaceae.

Chemical genetics is a multidisciplinary research method. In this study, it is used to screen compounds that promote aluminum-induced malate secretion in Arabidopsis thaliana. Inhibition of p38 mitogen-activated protein kinase (p38 MAPK; LY2228820) significantly increased the transcription of Arabidopsis thaliana aluminum-activated malate transporter 1 (AtALMT1) and sensitive to proton rhizotoxicity 1 (STOP1)-regulated genes, multidrug and toxic compound extrusion and aluminum sensitive 3, but not AtSTOP1 and the Al-biomarker genes At3g28510, At5g13320, suggesting that LY2228820 increased the early expression of STOP1-regulated genes without affecting AtSTOP1 expression. Inhibition of p38 MAPK (LY2228820) and Aurora A (MLN8237) increased aluminum-activated malate transport via AtALMT1, suggesting that both MLN8237 and LY2228820 interfere with AtALMT1 activity. An increase in root elongation was also observed in Arabidopsis after applying compounds LY2228820 and MLN8237. Thus, both LY2228820 and MLN8237 may play important roles in alleviating the inhibitory effects of aluminum on roots.

Various environmental conditions influence the characteristics of plant communities within wetlands. Although the influence of key environmental factors on plant community traits within specific types of wetland ecosystems has been studied extensively, how they regulate plant communities across marsh wetland types remains poorly understood. We examined how environmental conditions influence plant communities in marsh wetlands along the lower Tumen River in northeastern China. We collected and analyzed data on the plant community characteristics (species, height, and coverage), soil physicochemical properties (organic carbon, inorganic nitrogen, and sulfur), and climatic and topographic factors (temperature, precipitation, and elevation) of 56 distinct marsh plots (29 herbaceous, 14 shrub, and 13 forested marshes) to understand how these variables correlate with plant community characteristics across marsh types. The wetland plant diversity varied, with the lowest, intermediate, and highest diversity occurring in herbaceous, shrub, and forested marshes, respectively. Climate, topography, and soil properties had crucial influences on plant diversity and biomass. Structural equation modeling showed that, in herbaceous marshes, plant biomass was primarily determined by soil and plant diversity, with climate exerting an indirect effect. In shrub marshes, soil, climate, and plant diversity directly influenced biomass. In forest marshes, soil and plant diversity directly affected biomass, whereas climate and topography had indirect effects. These findings highlight the complex interactions among environmental factors across marsh ecosystems and their influence mechanisms on biomass, aiding in formulating effective conservation and restoration strategies for marsh wetland ecosystems.

UMAMIT proteins have been known as key players in amino acid transport. In Arabidopsis, functions of several UMAMITs have been characterized, but their precise mechanism, evolutionary history and functional divergence remain elusive. In this study, we conducted phylogenetic analysis of the UMAMIT gene family across key species in the evolutionary history of plants, ranging from algae to angiosperms. Our findings indicate that UMAMIT proteins underwent a substantial expansion from algae to angiosperms, accompanied by the stabilization of the EamA (the main domain of UMAMIT) structure. Phylogenetic studies suggest that UMAMITs may have originated from green algae and be divided into four subfamilies. These proteins first diversified in bryophytes and subsequently experienced gene duplication events in seed plants. Subfamily I was potentially associated with amino acid transport in seeds. Regarding subcellular localization, UMAMITs were predominantly localized in the plasma membrane and chloroplasts. However, members from clade 8 in subfamily III exhibited specific localization in the tonoplast. These members may have multiple functions, such as plant disease resistance and root development. Furthermore, our protein structure prediction revealed that the four-helix bundle motif is crucial in controlling the UMAMIT switch for exporting amino acid. We hypothesize that the specific amino acids in the amino acid binding region determine the type of amino acids being transported. Additionally, subfamily II contains genes that are specifically expressed in reproductive organs and roots in angiosperms, suggesting neofunctionalization. Our study highlights the evolutionary complexity of UMAMITs and underscores their crucial role in the adaptation and diversification of seed plants.