生命科学最新文献

TBL family proteins containing the domain of unknown function mainly act as xylan O-acetyltransferases, but the specific molecular mechanism of their functions remains unclear in plants (especially in cotton) so far. In this study, we characterized the TBL family proteins containing the conserved GDS and DxxH motifs in cotton (Gossypium hirsutum). Among them, GhTBL3 is highly expressed in fibers at the stage of secondary cell wall (SCW) formation and mainly functions as O-acetyltransferase to maintain acetylation of xylan in fiber SCW development. Overexpression of GhTBL3 in cotton promoted fiber SCW formation, resulting in increased fiber cell wall thickness. In contrast, suppression of GhTBL3 expression in cotton impaired fiber SCW synthesis, leading to the decreased fiber cell wall thickness, compared with wild type (WT). Furthermore, two fiber SCW-related transcription factors GhMYBL1 and GhKNL1 were found to directly bind to the promoter of GhTBL3 in cotton. GhMYBL1 enhanced the transcription activity of GhTBL3, whereas GhKNL1 inhibited the expression of GhTBL3 in fibers. The acetylation level of xylan was remarkably decreased in fibers of GhMYBL1 RNAi transgenic cotton, but the acetylation level of xylan was significantly increased in fibers of GhKNL1 RNAi cotton, relative to WT. Given together, the above results suggested that GhTBL3 may be under the dual control of GhMYBL1 and GhKNL1 to maintain the suitable acetylation level of xylan required for fiber SCW formation in cotton. Thus, our data provide an effective clue for potentially improving fiber quality by genetic manipulation of GhTBL3 in cotton breeding.

Symbiotic nitrogen fixation (SNF) profoundly alters plant and bacteroid metabolism; however, SNF impact on folates and one-carbon (1C) metabolism are unknown. To explore this, SNF was induced in Phaseolus Vulgaris with Rhizobium etli. Nodules accumulated the highest folate concentration yet reported in a plant tissue (60 nmol/g fresh weight). Folate upregulation was not exclusive of determinate nodules, moderate to high folate contents were also encounter in Medicago truncatula and sativa. Moreover, folates correlated partial and positively with N₂-fixation. 1C metabolism-associated amino acids (Ser, Gly, Cys, Thr, and Met) accumulated more in nodules than roots. Subcellular profiling of nodule folates revealed that the cytosol fraction primarily contained 5-methyl-tetrahydrofolate, cofactor for Met synthesis. 10-formyl-tetrahydrofolate, required for purine synthesis, was most abundant in nodule plastids, while bacteroids contained low folate levels. Differential transcriptome analysis from nodule legume studies revealed that only a few biosynthetic folate genes expression was increased in nodules whereas several genes for 1C reactions were upregulated. For the first time folates were detected in the xylem sap, with higher concentrations during SNF. We postulate that folates are needed during SNF to sustain purines, thymidylate, and Met synthesis, during both N₂-fixation and nodule growth; nodule metabolism is then a 1C-unit sink.

Understanding mechanisms driving tropical tree growth is essential for comprehending carbon sequestration and predicting the future of tropical forests amid rapid deforestation. We conducted a natural experiment in Mount Cameroon to identify climatic factors limiting diurnal and seasonal growth in dominant tree species across a 2200-m elevation gradient, from lowland rainforests to montane mist forests with distinct wet and dry seasons. Using high-precision automatic dendrometers, we recorded radial growth rates of 28 tropical tree species from 2015 to 2018, correlating them with rainfall (11 100-2500 mm) and temperatures (23-14°C) across elevations. Significant growth limitations were suggested at both extremes of water availability. Tree growth peaked during the dry and prewet seasons at humid lower elevations and during wet seasons at drier higher elevations. Growth rates increased with soil moisture at higher elevations and peaked at medium soil moisture at lower elevations. Trees grew fastest at lower temperatures relative to their elevation-specific means, with growth limited by high daytime temperatures and promoted by nighttime temperatures. Our results revealed significant interspecific diurnal and seasonal growth variations hindered by both water scarcity and excess in West African rainforests, essential for forecasting and modelling carbon sinks.

Soybean (Glycine max [L.] Merr.) is one of the world's most important sources of oil and vegetable protein. Much of the energy required for germination and early growth of soybean seeds is stored in fatty acids, mainly as triacylglycerols (TAGs), and the main seed storage proteins are β-conglycinin (7S) and glycinin (11S). Recent research advances have deepened our understanding of the biosynthetic pathways and transcriptional regulatory networks that control fatty acid and protein synthesis in organelles such as the plastid, ribosome and endoplasmic reticulum. Here, we review the composition and biosynthetic pathways of soybean oils and proteins, summarizing the key enzymes and transcription factors that have recently been shown to regulate oil and protein synthesis/metabolism. We then discuss the newest genomic strategies for manipulating these genes to increase the food value of soybeans, highlighting important priorities for future research and genetic improvement of this staple crop.

Plants are attacked by various insect herbivores. Upon attack-triggered biosynthesis of the phytohormone jasmonates (JAs), the JA receptor CORONATINE INSENSITIVE 1 recruits the JA-ZIM domain (JAZ) repressors for ubiquitination, releases the MYC-MYB transcription factor (TF) complexes, and enhances glucosinolates (GSs) biosynthesis to promote defense against insects in Arabidopsis. However, the negative regulation of JA-regulated defense remains largely unclear. Here, we found that Arabidopsis IVa bHLH TFs bHLH19 and bHLH20 interacted with JAZs. The bhlh19/20 mutations enhanced defense against the insects Spodoptera frugiperda and S. exigua, while their overexpression inhibited defense. bHLH19/20 repressed defense via at least two layers of regulation: first, bHLH19/20 interacted with the members MYC2/3/4/5 and MYB34/51/122 of MYC-MYB complexes, and inhibited the interaction/transcription activity of MYC2-MYB34; second, bHLH19/20 activated the RNA level of nitrile-specifier protein 1, which converts GSs into the less toxic nitriles. bhlh19/20 exhibited no penalty in JA-regulated growth inhibition. Collectively, our findings reveal the molecular mechanism for negatively regulating JA-mediated defense against insects in Arabidopsis without growth penalty by the pair of bHLH19/20 TFs.

Plants recognize molecules related to a variety of biotic stresses through pattern recognition receptors to activate plant immunity. In the interactions between plants and chewing herbivores, such as lepidopteran larvae, oral secretions (OS) are deposited on wounded sites, which results in the elicitation of plant immune responses. The widely conserved receptor-like kinase CHITIN ELICITOR RECEPTOR KINASE 1 (CERK1) has been broadly associated with the recognition of microbial components, such as fungal chitin, but its relevance to herbivory remained unclear. In this study, we used receptor-knockout rice (Oryza sativa) and larvae of the lepidopteran pest Mythimna loreyi to demonstrate that the induction of immune responses triggered by larval OS in rice cells largely depends on CERK1 (OsCERK1). CHITIN ELICITOR-BINDING PROTEIN (CEBiP), an OsCERK1-interacting receptor-like protein that was proposed as the main chitin receptor, also contributed to the responses of rice cells to OS collected from three different lepidopteran species. Furthermore, CEBiP knockout rice seedlings showed lower OS-triggered accumulation of jasmonic acid. These results strongly suggest that the OsCERK1 and CEBiP recognize a particular OS component in chewing lepidopteran herbivores, and point toward the presence of chitooligosaccharides in the OS. Targeted perturbation to chitin recognition, through the use of fungal effector proteins, confirmed the presence of chitooligosaccharides in the OS. Treatments of wounds on rice plants with chitooligosaccharides enhanced a set of immune responses, leading to resistance against an herbivorous insect. Our data show that rice recognizes chitooligosaccharides during larval herbivory to activate resistance, and identifies chitin as a novel herbivore-associated molecular pattern.

As tertiary gene pools of wheat, Aegilops comosa and Ae. caudata contain many excellent genes/traits and gradually become important and noteworthy wild resources for wheat improvement worldwide. However, the lack of molecular markers and cytological probes with good specificity and high sensitivity limits the development and utilization of Triticum aestivum-Ae. comosa (Ta. Aeco)/Ae. caudata (Ta. Aeca) introgression lines. Using specific-locus amplified fragment sequencing, two Ae. comosa and one Ae. caudata accessions, Chinese Spring, and three Ta. Aeco and Ta. Aeca introgression lines each were sequenced to develop new molecular markers and cytological probes. After strict sequence comparison and verification in different materials, a total of 39 molecular markers specific to three chromosomes in Ae. comosa (nine, seven, and 10 markers for 1M, 2M, and 7M, respectively) and Ae. caudata (two, six, and five markers for 3C, 4C, and 5C, respectively) and 21 fluorescence in situ hybridization (FISH) probes (one centromeric probe with signals specific to the M chromosomes, two centromeric probes with signals in all the tested genomes, and six, eight, and four FISH probes specific to the M, C, and M, C, and U chromosomes, respectively) were successfully exploited. The newly developed molecular markers and cytological probes could be used in karyotype studies, centromere evolutionary analyses of Aegilops, and had the ability to detect the fusion centromeres and small-fragment translocations in introgression lines.

Plasmodiophora brassicae, a soil-borne biotroph, establishes galls as strong physiological sinks on Brassicaceae plants including Brassica napus and Arabidopsis thaliana. We compare transcriptional profiles of phloem dissected from leaf petioles and hypocotyls of healthy and infected B. napus plants. Our results highlight how pathogenesis accompanies phloem-mediated defence responses whilst exerting a strong influence on carbon-nitrogen (C-N) economy. We observe transcriptional changes indicating decreased aliphatic glucosinolate biosynthesis, fluctuating jasmonic acid responses, altered amino acid (AA) and nitrate transport, carbohydrate metabolism and modified cytokinin responses. Changes observed in phloem-dissected from upper versus lower plant organs point to phloem as a conduit in mediating C-N repartitioning, nutrition-related signalling and cytokinin dynamics over long distances during clubroot disease. To assess changes in physiology, we measured AAs, sugars and cytokinins, in phloem exudates from B. napus plants. Despite the decrease in most AA and sucrose levels, isopentyl-type cytokinins increased within infected plants. Furthermore, we employed Arabidopsis for visualising promoter activities of B. napus AA and N transporter orthologues and tested the impact of disrupted cytokinin transport during P. brassicae-induced gall formation using Atabcg14 mutants. Our physiological and microscopy studies show that the host developmental reaction to P. brassicae relies on cytokinin and is accompanied by intense nitrogen and carbon repartitioning. Overall, our work highlights the systemic aspects of host responses that should be taken into account when studying clubroot disease.

The increase in global climate variability has increased the frequency and severity of floods, profoundly affecting agricultural production and food security worldwide. Autophagy is an intracellular catabolic pathway that is dispensable for plant responses to submergence. However, the physiological role of autophagy in plant response to submergence remains unclear. In this study, a multi-omics approach was applied by combining transcriptomics, proteomics, and lipidomics to characterize molecular changes in the Arabidopsis autophagy-defective mutant (atg5-1) responding to submergence. Our results revealed that submergence resulted in remarkable changes in the transcriptome, proteome, and lipidome of Arabidopsis. Under submerged conditions, the levels of chloroplastidic lipids, including monogalactosyldiacylglycerol (MGDG), digalactosyldiacylglycerol (DGDG), and phosphatidylglycerol (PG), were lower in atg5-1 than in wild-type, suggesting that autophagy may affect photosynthesis by regulating lipid metabolism. Consistently, photosynthesis-related proteins and photosynthetic efficiency decreased in atg5-1 under submergence conditions. Phenotypic analysis revealed that inhibition of photosynthesis resulted in a decreased tolerance to submergence. Compared to wild-type plants, atg5-1 plants showed a significant decrease in starch content after submergence. Collectively, our findings reveal a novel role for autophagy in plant response to submergence via the regulation of underwater photosynthesis and starch content.

Galloylated catechins in tea leaves, primarily epigallocatechin-3-gallate (EGCG) and epicatechin gallate (ECG), possess prominent biological activities. It is well established that EGCG and ECG are abundantly present in tender leaves but are less prevalent in mature leaves. However, the fundamental regulatory mechanisms underlying this distribution remain unknown. In this study, we integrated transcriptome data and catechin component levels in tea leaves from six leaf positions using weighted gene co-expression network analysis. This analysis revealed a positive correlation between variations in CsWRKY12 expression and EGCG and ECG levels. Further investigation using yeast one-hybrid and dual-luciferase assays, as well as electrophoretic mobility shift assay, demonstrated that CsWRKY12 activated the transcription of CsSCPL4 and CsSCPL5, which encode enzymes responsible for galloylated catechins biosynthesis, by directly binding to W-box elements in their promoters. Overexpression of CsWRKY12 in tea leaves promoted the expression of CsSCPL4 and CsSCPL5, leading to an increase in EGCG and ECG content. Moreover, we found that a VQ motif-containing protein, CsVQ4L, interacted with CsWRKY12 and facilitated its transcriptional function by regulating the expression of CsSCPL4 and CsSCPL5. Collectively, our findings suggest that the interaction between CsWRKY12 and CsVQ4L contributes to the accumulation of galloylated catechins in tender leaves of tea plants.