Explore the vast range of titles available.

Background Plant responses to biotic and abiotic stresses are complex processes. Previous studies have shown that the LBD gene family plays important roles in plant growth and development as well as in plant defense against biotic and abiotic stresses. The expression of LBD genes was investigated in walnuts under biotic and abiotic stresses, revealing that LBD38-1 may be a key gene in the plant stress response. This study provides new insights into the roles of LBD genes in plant responses to biotic stress. Results Forty-nine members of the JrLBD gene family were identified in the walnut genome and classified into six subfamilies. Comparative homology analysis through phylogenetic trees revealed that the presence of Group I-a and Group VI plays an important role in resistance to stressors. The expression of walnut LBD genes under cold-temperature, high-temperature, mechanical damage, and biotic stresses was analyzed via transcriptome sequencing, and the expression of JrLBD38-1 in the Group VI subfamily was particularly prominent. According to transcriptome profile analysis, JrLBD38-1 is highly expressed in different tissues of walnuts, suggesting that it plays a regulatory role in the growth and development of different tissues. The function of the Gibberellin (GA) response element in the JrLBD38-1 promoter was further analyzed and verified. These findings confirmed that GA regulated JrLBD38-1 expression changes during Xanthomonas arboricola pv. juglandis infestation of walnut leaves. Conclusion Forty-nine walnut JrLBDs were identified and classified into six subfamilies. JrLBD38-1 has GA-inducible expression, is regulated by GA under pathogenic bacterial stress, and is involved in the response to biotic stress. This function of JrLBD38-1 provides new insights into walnut disease resistance mechanisms.

Background Tissue culture is an effective method for the rapid breeding of seedlings and improving production efficiency, but explant browning is a key limiting factor of walnut tissue culture. Specifically, the polymerization of PPO-derived quinones that cause explant browning of walnut is not well understood. This study investigated explants of ‘Zanmei’ walnut shoot apices cultured in agar (A) or vermiculite (V) media, and the survival percentage, changes in phenolic content, POD and PPO activity, and JrPPO expression in explants were studied to determine the role of PPO in the browning of walnut explants. Results The results showed that the V media greatly reduced the death rate of explants, and 89.9 and 38.7% of the explants cultured in V media and A media survived, respectively. Compared with that of explants at 0 h, the PPO of explants cultured in A was highly active throughout the culture, but activity in those cultured in V remained low. The phenolic level of explants cultured in A increased significantly at 72 h but subsequently declined, and the content in the explants cultured in V increased to a high level only at 144 h. The POD in explants cultured in V showed high activity that did not cause browning. Gene expression assays showed that the expression of JrPPO1 was downregulated in explants cultured in both A and V. However, the expression of JrPPO2 was upregulated in explants cultured in A throughout the culture and upregulated in V at 144 h. JrPPO expression analyses in different tissues showed that JrPPO1 was highly expressed in stems, young leaves, mature leaves, catkins, pistils, and hulls, and JrPPO2 was highly expressed in mature leaves and pistils. Moreover, browning assays showed that both explants in A and leaf tissue exhibited high JrPPO2 activity. Conclusion The rapid increase in phenolic content caused the browning and death of explants. V media delayed the rapid accumulation of phenolic compounds in walnut explants in the short term, which significantly decreased explants mortality. The results suggest that JrPPO2 plays a key role in the oxidation of phenols in explants after branch injury.

The authors would like to make the following correction to their published paper [...]

Background: Walnut (Juglans regia L.) is a species of considerable ecological, social, and economic importance. However, comprehensive metabolomic investigations into walnut cultivars under chilling stress remain scarce. Methods: In this study, we utilized LC-MS/MS-based non-targeted metabolomics to analyze differential metabolites in two walnut cultivars exposed to chilling stress at 0.5 °C for 0 and 48 h. Results: A total of 1504 metabolites were identified, including 871 in positive ion mode and 633 in negative ion mode. Specifically, 160 and 287 differential metabolites were detected in ‘Qingxiang’ and ‘Liaoning No.8’, respectively, under positive ion mode. In negative ion mode, 83 and 206 differential metabolites were identified in ‘Qingxiang’ and ‘Liaoning No.8’, respectively. These metabolites were primarily associated with α-linolenic acid metabolism, phenylpropanoid biosynthesis, flavonoid biosynthesis, and phenylalanine metabolism, and multiple candidate genes were obtained that exhibit significant correlations with metabolites, suggesting their critical roles in the walnut’s response to chilling stress. Conclusions: This study proposes a metabolic network for walnut leaves under chilling stress, enriching our understanding of the metabolic adaptation mechanisms of walnuts to low-temperature conditions. It lays a foundation for investigating the regulatory mechanisms of metabolite synthesis under cold stress and provides important theoretical insights for breeding cold-resistant walnut cultivars.

Apple trees grafted on different rootstock types, including vigorous rootstock (VR), dwarfing interstock (DIR), and dwarfing self-rootstock (DSR), are widely planted in production, but the molecular determinants of tree branch architecture growth regulation induced by rootstocks are still not well known. In this study, the branch growth phenotypes of three combinations of 'Fuji' apple trees grafted on different rootstocks (VR: Malus baccata; DIR: Malus baccata/T337; DSR: T337) were investigated. The VR trees presented the biggest branch architecture. The results showed that the sugar content, sugar metabolism-related enzyme activities, and hormone content all presented obvious differences in the tender leaves and buds of apple trees grafted on these rootstocks. Transcriptomic profiles of the tender leaves adjacent to the top buds allowed us to identify genes that were potentially involved in signaling pathways that mediate the regulatory mechanisms underlying growth differences. In total, 3610 differentially expressed genes (DEGs) were identified through pairwise comparisons. The screened data suggested that sugar metabolism-related genes and complex hormone regulatory networks involved the auxin (IAA), cytokinin (CK), abscisic acid (ABA) and gibberellic acid (GA) pathways, as well as several transcription factors, participated in the complicated growth induction process. Overall, this study provides a framework for analysis of the molecular mechanisms underlying differential tree branch growth of apple trees grafted on different rootstocks.

Nitrogen (N) and phosphorus (P) are essential phytomacronutrients, and deficiencies in these two elements limit growth and yield in apple ( Malus domestica Borkh.). The rootstock plays a key role in the nutrient uptake and environmental adaptation of apple. The objective of this study was to investigate the effects of N and/or P deficiency on hydroponically-grown dwarfing rootstock ‘M9-T337’ seedlings, particularly the roots, by performing an integrated physiological, transcriptomics-, and metabolomics-based analyses. Compared to N and P sufficiency, N and/or P deficiency inhibited aboveground growth, increased the partitioning of total N and total P in roots, enhanced the total number of tips, length, volume, and surface area of roots, and improved the root-to-shoot ratio. P and/or N deficiency inhibited NO 3   − influx into roots, and H + pumps played a important role in the response to P and/or N deficiency. Conjoint analysis of differentially expressed genes and differentially accumulated metabolites in roots revealed that N and/or P deficiency altered the biosynthesis of cell wall components such as cellulose, hemicellulose, lignin, and pectin. The expression of MdEXPA4 and MdEXLB1 , two cell wall expansin genes, were shown to be induced by N and/or P deficiency. Overexpression of MdEXPA4 enhanced root development and improved tolerance to N and/or P deficiency in transgenic Arabidopsis thaliana plants. In addition, overexpression of MdEXLB1 in transgenic Solanum lycopersicum seedlings increased the root surface area and promoted acquisition of N and P, thereby facilitating plant growth and adaptation to N and/or P deficiency. Collectively, these results provided a reference for improving root architecture in dwarfing rootstock and furthering our understanding of integration between N and P signaling pathways.

Background The walnut shell, which is composed of a large number of sclereids originating from the lignified parenchyma of the endocarp, plays an important role in fruit development and during harvesting and storage. The physical and chemical properties of walnut shells are closely related to the lignin content. Laccase is the key enzyme responsible for lignin biosynthesis by the polymerization of monolignols and plays crucial roles in secondary cell wall formation in plants. In this study, we screened and identified laccase family genes from the walnut genome and investigated the expression of laccase during endocarp lignification in walnut. Results A total of 37 laccase genes were screened from the walnut genome and distributed on nine chromosomes and classified into 6 subfamilies, among which subfamily IV showed distinct expansion. We observed that endocarp lignification started 44 days after flowering (DAF), and at later periods, the lignin content increased rapidly, with growth peaks at 44–50 DAF and 100–115 DAF. The lignification of the endocarp proceeded from the outside to the inside, as demonstrated by section staining in combination with endocarp staining. Furthermore, the changes in the expression of laccase family genes in the endocarp at different developmental stages were studied, and JrLACs showed different expression trends. The expression of nine genes showed significant increase after 44 DAF, and among these, JrLAC12–1 , JrLAC12–2 and JrLAC16 showed a significant change in expression at the lignification stage. A study of the expression of JrLACs in different tissues and at various endocarp developmental stages revealed, that most JrLACs were expressed at low levels in mature tissues and at high levels in young tissues, in particular, JrLAC12–1 showed high expression in the young stems. A significant positive correlation was found between the expression of JrLAC12–1 and the variation in the lignin content in the endocarp. Conclusion Laccase genes play an important role in the lignification of the walnut endocarp, and JrLACs play different roles during fruit development. This study shows that JrLAC12–1 may play a key role in the lignification of endocarp.

Peach trees exhibit vigorous growth that is often difficult to manage, frequently leading to canopy closure and the outward migration of fruiting positions, which ultimately results in diminished yield and fruit quality. Therefore, it is of great importance to study the key genes regulating peach tree vigor. Preliminary experiments identified PpNAC036 as a candidate gene potentially associated with vigor. In this study, we characterized the expression profile of PpNAC036 across various peach tissues. Our results demonstrate that PpNAC036 is most highly expressed in stems and responds rapidly to hormonal treatments, with expression levels increasing 3.6-fold and 3.9-fold under IAA and NPA treatments, respectively (5 min to 1 h). Subsequently, the PpNAC036 gene was cloned and overexpressed in Arabidopsis thaliana. Compared to the wild type, transgenic Arabidopsis exhibited a 28–50% reduction in primary root length and a 31.6–36.8% decrease in hypocotyl length. Conversely, at maturity, the transgenic Arabidopsis displayed enhanced vegetative vigor, with fresh and dry weights increasing by 37–48% and 29–46%, respectively. This growth was accompanied by a nearly two-fold increase in stem diameter and a 1.5- to 2-fold elevation in lignin content; simultaneously, genes related to lignin biosynthesis were upregulated. Hormonal profiling revealed that PpNAC036 overexpression led to a 7-fold increase in IAA, a 22–60% rise in GAs, and a 97–106% increase in CTKs, whereas ABA levels decreased by 5–6%. Furthermore, the transgenic Arabidopsis exhibited delayed germination and flowering, along with alterations in the number of floral organs. Transcriptomic analysis identified 2797 common DEGs, which were enriched in pathways related to cell wall organization and hormone signaling. Collectively, these findings elucidate the function of PpNAC036 as a pivotal regulator of plant vigor and secondary cell wall development, positioning it as a promising candidate gene for molecular breeding and architectural optimization in peach.

Organic acids are naturally present in plants and exert a positive influence on plant development, which justifies surveying their potential effect on adventitious root (AR) formation. In this study, 0.0298 mol/L (4000 mg/L) of malic acid and 0.0267 mol/L (4000 mg/L) of tartaric acid were used to explore the effects of low-molecular-weight organic acid on the rooting of persimmon rootstock Diospyros lotus L. during cutting propagation. After organic acid treatment, the rooting percentage and the survival rate significantly increased, accompanied by a greater development of lateral roots. Anatomical analysis revealed that Diospyros lotus L. exhibits characteristics that induce root primordia, and organic acid treatment can enhance the differentiation of root primordia. Furthermore, treatment with organic acid led to a substantial decrease in soluble sugar and starch contents, along with a slight increase in soluble protein content during early cutting stages. Additionally, the indole-3-acetic acid (IAA) content peaked in the early stages of AR formation and was significantly higher than that of the control, while abscisic acid (ABA) levels exhibited the opposite trend. Comparatively, gibberellic acid (GA3) remained at extremely low levels throughout the rooting process in the organic acid groups compared to the control. In conclusion, the current study uncovers the anatomical structure over time during AR formation, revealing the dynamic changes in the related main nutrients and hormones and providing new ideas and a new practical approach for improving root regeneration in persimmon rootstock cuttings.

Summary Allele‐specific expression (ASE) can lead to phenotypic diversity and evolution. However, the mechanisms regulating ASE are not well understood, particularly in woody perennial plants. In this study, we investigated ASE genes in the apple cultivar ‘Royal Gala’ (RG). A high quality chromosome‐level genome was assembled using a homozygous tetra‐haploid RG plant, derived from anther cultures. Using RNA‐sequencing (RNA‐seq) data from RG flower and fruit tissues, we identified 2091 ASE genes. Compared with the haploid genome of ‘Golden Delicious’ (GD), a parent of RG, we distinguished the genomic sequences between the two alleles of 817 ASE genes, and further identified allele‐specific presence of a transposable element (TE) in the upstream region of 354 ASE genes. These included MYB110a that encodes a transcription factor regulating anthocyanin biosynthesis. Interestingly, another ASE gene, MYB10 also showed an allele‐specific TE insertion and was identified using genome data of other apple cultivars. The presence of the TE insertion in both MYB genes was positively associated with ASE and anthocyanin accumulation in apple petals through analysis of 231 apple accessions, and thus underpins apple flower colour evolution. Our study demonstrated the importance of TEs in regulating ASE on a genome‐wide scale and presents a novel method for rapid identification of ASE genes and their regulatory elements in plants.