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Parthenocarpy can be induced by gibberellin (GA) treatment in plants. The fruits of the loquat exhibit many seeds. GA treatment can induce the development of seedless fruit and increase fruit quality during production. However, the molecular mechanism of fruit setting under GA treatment is still unclear. Our aim was to explore GA-induced parthenocarpy in triploid loquat by proteome analysis to identify the differentially expressed proteins. A proteome analysis was performed using TMT protein labeling and LC-MS/MS in triploid loquat. A total of 7290 protein groups were identified in the two stages of fruit setting. The quantitative results showed that 923 differentially expressed proteins (DEPs) were isolated, which were enriched in five pathways: ribosome, citrate cycle (TCA cycle), pentose phosphate, carbon metabolism, and carbon fixation. Twenty-four DEPs were annotated as putative key regulatory proteins involved in fruit setting, which were related to the auxin response, gibberellin metabolism, ethylene synthesis, and cell division. In addition, thirty-five DEPs were involved in the formation of the cell wall, which might be downstream proteins involved in cell proliferation during fruit setting. Our report reveals new insight into the protein dynamics of loquat fruit setting induced by GA treatment via the analysis of proteome profiles and provides a reference for other Rosaceae species.

Flowering is an important phenophase of plant species, however, knowledge about the regulatory mechanism controlling flowering cues in loquat is limited. To identify candidate genes regulating flowering time in loquat, we used RNA-Seq technology to conduct a comparative transcriptome analysis of differentiating apical buds collected from the early-flowering variety ‘Baiyu’ and the late-flowering variety ‘Huoju’. A total of 28,842 differentially expressed transcripts (DETs) were identified. Of these, 42 DETs controlled flowering time while 17 other DETs were associated with the ABA signaling pathway. Compared with those in ‘Huoju’, EjFT, EjFY, EjFLK, and EjCAL1-like were significantly upregulated in ‘Baiyu’. Moreover, transcripts of the ABA 8′-hydroxylases (EjABH2, EjABH4, and EjABH4-like2), the ABA receptors (EjPYL4/8), and the bZIP transcription factor EjABI5-like were upregulated in ‘Baiyu’ compared with ‘Huoju’. Hence, they might regulate loquat flowering time. There was no significant difference between ‘Baiyu’ and ‘Huoju’ in terms of IAA content. However, the ABA content was about ten-fold higher in the apical buds of ‘Baiyu’ than in those of ‘Huoju’. The ABA:IAA ratio sharply rose and attained a peak during bud differentiation. Thus, ABA is vital in regulating floral bud formation in loquat. The results of the present study help clarify gene transcription during loquat flowering.

Grafting is a common method of variety propagation in loquat breeding, the slow growth of rootstocks is a main factor limiting the expansion of this technique. This study aimed to evaluate the effects of seven different fertilizer formulas on the growth of loquat rootstock seedlings, five water-soluble fertilizer formulas, as well as organic fertilizer and controlled-release fertilizer were evaluated. An unfertilized control (CK) was also performed. Growth indicators including plant height, stem thickening and lignification, leaf area, root development, dry matter accumulation, spatial distribution of nutrient elements, and cross-sectional anatomy of stem were measured. The results showed that the addition of microelements in fertilizer could significantly delay the lignification process of the cambium, which exhibiting the greatest improvement in stem thickening. Phosphorus nutrition could significantly promote the occurrence of fibrous roots, while excessive phosphorus supply might disturb the absorption and utilization of nitrogen of roots, intensify the lignification process of the main stem, and then affect the growth of the aboveground part. The findings of this research could provide a theoretical basis for identifying an optimum fertilization formula and technique for promoting the rapid growth and accelerating the lignification process at different stages of loquat rootstock seedling growth.

Aluminum (Al) toxicity associated with acid soils represents one of the biggest limitations to crop production worldwide. The root apex of plants is the major perception site of Al toxicity. In Al stressed wheat primary roots, Al accumulation and loss of plasma membrane integrity were highest in the root apex (0–5 mm), and decreased along the root axis (5–25 mm). To further understand these responses in wheat, spatial profiles of antioxidant responses to Al along the 0–25 mm root tip of two wheat genotypes differing in Al tolerance were analyzed. Under Al stress, the lowest root elongation was in the 0–5 mm root tip, and more severe inhibition was observed in Al-sensitive genotype than Al-tolerant genotype. The highest increase of Al and hydrogen peroxide (H2O2) was in the 0–5 mm zone, with the most pronounced increase of malondialdehyde content and Evans blue uptake after Al exposure, especially in Al-sensitive genotype. The activities of superoxides dismutase (SOD), ascrobate peroxidase (APX), catalase (CAT) and peroxidase (POD) and levels of antioxidants (ascorbic acid, reduced glutathione, dehydroascorbate, glutathione disulfide) were significantly increased along the root tip under Al stress, with the 0–5 mm region again being the most active zone. In the same zone, the activities of CAT, APX and contents of antioxidants were higher in Al-tolerant genotype while SOD and POD activities were lower. Our results indicate that Al-induced changes in H2O2 production and antioxidative system in root tip are regulated in a spatially-specific manner, suggesting that this response may play an important role in wheat adaptation to Al toxicity.

Vegetative propagation by cuttings is a very popular method. However, blueberry propagation using cuttings is still a main factor limiting its expansion because its results can vary according to the blueberry cultivar and environmental factors. This study aimed to evaluate the rooting abilities of hardwood cuttings for six blueberry cultivars (O’Neal, Misty, Diana, Biloxi, Bluebeauty, and Coville) using three different exogenous indole-butyric acid (IBA) concentrations (1000, 2000, and 3000 ppm), and to determine if the cutting position (basal, central, apical) affects rooting performance. A control treatment (0 ppm IBA) was also performed. After 90 days of each treatment, rooting percentage, average root length, and average root number per cutting were assessed and used to calculate rooting index, which is a measure of rooting ability. The rooting percentages of hardwood cuttings differed largely among cultivars and were highest for ‘Bluebeauty’ (68.55%), followed by ‘Biloxi’ (68.01%). The rooting index values of these two cultivars (33.59 and 35.18, respectively) were significantly higher than those of the other four cultivars. The rooting response of blueberry hardwood cuttings to IBA concentrations was quadratic, and 1000 and 2000 ppm IBA were sufficient to express the maximum rooting percentage in most cultivars. The rooting abilities of basal, central, and apical cuttings were similar with treatments with high IBA concentrations. The effects of the cultivar, IBA concentration, and interaction between them on rooting percentage, average root length, and average root number were significant; however, the effects of the cutting position on the rooting percentage and average root length were not. This suggested that the rooting abilities of blueberry hardwood cuttings were significantly influenced by the cultivar and IBA concentration rather than by the cutting position.