Next Article in Journal
Retinal Neurodegeneration in an Intraocular Pressure Fluctuation Rat Model
Previous Article in Journal
The Potential of Natural Carotenoids-Containing Sericin of the Domestic Silkworm Bombyx mori
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Exogenous Melatonin Application Accelerated the Healing Process of Oriental Melon Grafted onto Squash by Promoting Lignin Accumulation

1
College of Horticulture, Shenyang Agricultural University, Shenyang 110866, China
2
Key Laboratory of Protected Horticulture (Ministry of Education), Shenyang Agricultural University, Shenyang 110866, China
3
Modern Protected Horticultural Engineering & Technology Center, Shenyang Agricultural University, Shenyang 110866, China
4
Key Laboratory of Horticultural Equipment (Ministry of Agriculture and Rural Affairs), Shenyang Agricultural University, Shenyang 110866, China
5
College of Horticulture, Hunan Agricultural University, Changsha 410128, China
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2024, 25(7), 3690; https://doi.org/10.3390/ijms25073690
Submission received: 28 February 2024 / Revised: 24 March 2024 / Accepted: 24 March 2024 / Published: 26 March 2024
(This article belongs to the Special Issue Advances in Research on Fruit Crop Breeding and Genetics 3.0)

Abstract

:
Melatonin (MT) is a vital hormone factor in plant growth and development, yet its potential to influence the graft union healing process has not been reported. In this study, we examined the effects of MT on the healing of oriental melon scion grafted onto squash rootstock. The studies indicate that the exogenous MT treatment promotes the lignin content of oriental melon and squash stems by increasing the enzyme activities of hydroxycinnamoyl CoA ligase (HCT), hydroxy cinnamaldehyde dehydrogenase (HCALDH), caffeic acid/5-hydroxy-conifer aldehyde O-methyltransferase (COMT), caffeoyl-CoA O-methyltransferase (CCoAOMT), phenylalanine ammonia-lyase (PAL), 4-hydroxycinnamate CoA ligase (4CL), and cinnamyl alcohol dehydrogenase (CAD). Using the oriental melon and squash treated with the exogenous MT to graft, the connection of oriental melon scion and squash rootstock was more efficient and faster due to higher expression of wound-induced dedifferentiation 1 (WIND1), cyclin-dependent kinase (CDKB1;2), target of monopteros 6 (TMO6), and vascular-related NAC-domain 7 (VND7). Further research found that the exogenous MT increased the lignin content of the oriental melon scion stem by regulating CmCAD1 expression, and then accelerated the graft healing process. In addition, the root growth of grafted seedlings treated with the exogenous MT was more vigorous.

1. Introduction

Grafting technology can potentially enhance the resistance of plants against both biotic and abiotic stresses, mitigate soil-borne diseases, and overcome the challenges of continuous cropping. This technique has been extensively utilized in cultivating fruits and vegetables [1,2]. The oriental melon is a variety of melon with rich nutritional value and excellent taste. However, fusarium wilt disease occurs severely in production. Grafting is one of the most effective methods to prevent fusarium wilt disease in greenhouse melon production. Currently, grafting cultivation of melons has been widely adopted in production. It is widely recognized that the establishment of successful healing of rootstocks and scions is a crucial prerequisite for the cultivation of grafted seedlings. The healing process in grafted plants is a complex physiological mechanism that involves formation of isolation layers, callus generation, and vascular bundle reconnection [3]. According to Tan et al. [4], melatonin (MT) is currently recognized for its potent antioxidant function as an endogenous scavenger of free radicals. Meanwhile, it also plays a significant role in the growth and development of plants by enhancing seed germination, promoting root growth, and regulating callus formation [5,6,7]. Exogenous MT could effectively improve the ability of plants to resist biotic and abiotic stresses. Studies have demonstrated that the application of exogenous MT could amplify the resistance and drought resistance of apple plants to apple fruit spot disease and enhance the heat resistance of Arabidopsis and the low-temperature resistance of Rhodiola and Ulmus pumila [8,9,10,11,12,13]. However, it remains unknown whether exogenous MT application can regulate the graft union healing process of the plants.
Recent studies have reported that exogenous MT could significantly promote plant lignin accumulation [14,15,16]. Lignin played an essential role in plant growth and development and was actively involved in plant responses to various environmental stresses in [17,18,19,20]. The synthesis of lignin was significantly regulated by the enzyme activity of cinnamyl alcohol dehydrogenase (CAD), which was found to be an essential enzyme in the lignin synthesis pathway. However, it is even unclear whether exogenous MT treatment might improve lignin accumulation by inducing the up-regulated expression of CmCADs in melon. Furthermore, transcriptome analysis on grafted litchi chinensis and grafted melon showed that genes related to lignin biosynthesis were differentially expressed during the graft union healing process [21,22]. We speculated that lignin might be involved in the healing of graft unions, but further studies were required to back this up. Specifically expressed genes at the graft union of plants participated in a series of physiological and biochemical processes during graft healing, such as some genes involved in secondary cell metabolism, cell wall synthesis, vascular tissue reconnection, and other functions [23]. Recently, many key factors have been identified as regulating the graft union healing of plants. The genes of WIND1-4 were crucial in regulating wound-induced callus formation by promoting cellular dedifferentiation and proliferation [24,25]. The genes of WOX played an essential role in many physiological processes, including root and stem apical meristem formation, organ development, and vascular tissue development [26,27,28,29]. SlWOX4 potentially regulated the compatibility of scion and rootstock, which was crucial for vascular bundle reconnection in the graft union healing of plants [30]. TMO6 was closely related to callus formation and vascular regeneration of grafted unions during the healing process [31], and VND7 directly or indirectly induced the expression of some genes associated with xylem vessel element differentiation [32,33]. However, it has not been reported whether exogenous MT application could affect graft union healing by regulating the expression of these genes related to graft union healing.
In this study, we applied the exogenous MT to treat the oriental melon scion and squash rootstock seedlings and investigated the effects of the exogenous MT on lignin accumulation and graft union healing process. Furthermore, we hope to provide a theoretical and practical basis for regulating graft union healing by the exogenous MT.

2. Results

2.1. Identification of Members of the CmGH9B Gene Family Members

We found that exogenous MT treatment could significantly increase the lignin contents of oriental melon and squash seedling stems (Figure 1A). The enzyme activities related to lignin biosynthesis, like HCT, HCALDH, COMT, CCoAOMT, 4CL, and CAD, were determined. The results showed that the HCT (Figure 1B), HCALDH (Figure 1C), COMT (Figure 1D), CCoAOMT (Figure 1E), and CAD activities (Figure 1H) of the oriental melon and squash seedling stems were increased by the exogenous MT treatment. The PAL activities (Figure 1F) of the oriental melon seedling stems were increased by exogenous MT treatment. However, exogenous MT did not significantly affect the 4CL activities of the oriental melon scion and squash seedling stems (Figure 1G). The exogenous MT applications could promote lignin accumulation in stems of oriental melon and squash seedlings by increasing enzyme activities related to lignin biosynthesis.

2.2. Historic Observation of the Graft Union Healing Process of the Oriental Melon Scion Grafted onto Squash Rootstock by the Exogenous MT Treatment

In the acid fuchsin absorption experiment, the oriental melon scion and squash rootstock seedlings treated with the exogenous MT were used to graft. As the oriental melon scion and squash rootstock gradually heal, acid fuchsin will move along the vascular bundle and eventually appear red in the stem tissue sections of the oriental melon scion. At 8 DAG, we distinctly observed the acid fuchsin in the stem tissue sections of the exogenous MT treatment. However, it appeared in the stem tissue sections of the control at 9 DAG (Figure 2). To further investigate the effect of exogenous MT treatment on graft healing, we conducted the paraffin section test. Under the exogenous MT treatment, the callus formation happened at 5 DAG, and the vascular bundles connected at 8 DAG. However, the callus formed at 6 DAG and the vascular bundles joined at 9 DAG in the control (Figure 3). So, the exogenous MT treatment not only promoted the lignin content of oriental melon and squash seedlings but also accelerated the graft union healing process.

2.3. Expression Profiles of the Genes Related to Graft Union Healing of the Oriental Melon Scion Grafted onto Squash Rootstock by the Exogenous MT Treatment

To further analyze the effects of exogenous MT treatment on the graft union healing process, we determined the expression of the genes related to healing, including WOUND-INDUCED DEDIFFERENTIATION1 (WIND1), WUSCHEL-RELATED HOMEOBOX4 (WOX4), CYCLIN-DEPENDENT KINASE (CDKB1;2), TARGET of MONOPTEROS 6 (TMO6), and VASCULAR-RELATED NAC-DOMAIN 7 (VND7) of the oriental melon and squash rootstock (Figure 4 and Figure 5). The relative expression levels of CmWIND1 of oriental melon (Figure 4A) and CmoWIND1 of squash rootstock (Figure 5A) increased gradually from NG to 2 DAG. The relative expression levels of CmWIND1 in the oriental melon scion treated with exogenous MT were significantly higher than the control at 2 DAG. The relative expression levels of CmoWIND1 in the squash rootstock treated with exogenous MT were also significantly higher than the control at 1 and 2 DAG. There was no significant difference in the relative expression levels of CmWOX4 between MT and control, even though they increased from 1 to 3 DAG (Figure 4B). And the relative expression levels of CmoWOX4 in the squash rootstock treated with exogenous MT were significantly higher than the control at 1 DAG (Figure 5B). From 4 to 6 DAG, the relative expression levels of CmCDKBB1;2 showed a decreasing trend (Figure 4C), and the relative expression levels of CmoCDKB1;2 showed an increasing trend (Figure 5C).
However, the exogenous MT treatment significantly improved the relative expression levels of CmCDKB1;2 and CmoCDKB1;2 at 6 DAG. From 6 to 8 DAG, the relative expression levels of CmTMO6 first increased and then decreased. Those of the oriental melon scion treated with exogenous MT were significantly higher than the control at 6 and 7 DAG (Figure 4D). The relative expression levels of CmoTMO6 changed slightly, and the exogenous MT significantly improved the relative expression levels of CmoTMO6 at 6 DAG (Figure 5D). From 8 to 10 DAG, the relative expression levels of CmVND7 in oriental melon scion treated with the exogenous MT were maintained at high levels. They were significantly higher than the control at 8 and 9 DAG (Figure 4E). Then, the relative expression levels of CmoVND7 in the squash rootstock treated with the exogenous MT were significantly higher than the control at 8 DAG (Figure 5E).

2.4. Expression Profiles and Functions of CmCADs during the Graft Healing Process of Oriental Melon Scion Grafted onto Squash Rootstock by the Exogenous MT Treatment

CAD is the rate-limiting enzyme in lignin biosynthesis. We identified the CmCAD1, CmCAD2, CmCAD3, and CmCAD4 from the melon genome. We detected their expression profiles from 2 to 9 DAG (Figure 6).
At 2 DAG, the relative expression levels of CmCAD1, CmCAD2, CmCAD3, and CmCAD4 by the exogenous MT treatment were significantly higher than the control. Moreover, their relative expression levels significantly declined at 5 DAG. From 5 to 9 DAG, the relative expression levels of CmCAD1 gradually increased. The exogenous MT treatment significantly improved CmCAD1 expression, except for 5 DAG (Figure 6A). The relative expression levels of CmCAD2 by the exogenous MT treatment were markedly higher than the control at 5 and 6 DAG (Figure 6B). The relative expression levels of CmCAD3 and CmCAD4 by the exogenous MT treatment were significantly higher than the control at 6 DAG and 8 DAG, respectively (Figure 6C,D). However, their relative expression levels were markedly lower than the control at 9 DAG. According to the results, we concluded that CmCAD1 was a crucial gene in lignin biosynthesis and involved in the graft union healing process.
To further verify the function of CmCAD1 during the graft union healing of oriental melon scion grafted onto squash rootstock, we performed a transient silencing assay of CmCAD1 in the oriental melon scion stems. The results indicated that the CmCAD1 expression levels in the transiently silenced oriental melon stem were significantly lower than the control during the graft healing process (Figure 7B), and the lignin content of those was also markedly lower than the control (Figure 7A). In addition, we found that the acid fuchsin was observed in the at 9 DAG and in the control at 8 DAG. Furthermore, we found that there were more acid fuchsins in the control than in the TRV-CmCAD1 at 10 DAG (Figure 8). Obviously, the vascular connectivity of the TRV-CmCAD1 was weaker than the control. In conclusion, CmCAD1 might affect the graft union healing of oriental melon scion grafted onto squash rootstock by regulating lignin biosynthesis.

2.5. Effects of the Exogenous MT Treatment on the Grafted Seedling Root Growth of Oriental Melon Scion Grafted onto Squash Rootstock

The quality of the grafted seedlings is a key factor in achieving a high quality and yield of oriental melon. In this study, we also analyzed the root growth characteristics of five-leaf grafted seedlings treated with exogenous MT using the root system scanner (Figure 9A). The results indicated that the root length (Figure 9B), root surface area (Figure 9C), root average diameter (Figure 9D), the total number of root tips (Figure 9E), and root forks of grafted seedlings treated with exogenous MT (Figure 9F) were all significantly higher than those of the control. The roots of the exogenous MT-treated seedlings grew better than those of the control.

3. Discussion

The phenylpropane metabolic pathway was the most important metabolic pathway in plant resistance to biotic and abiotic stresses, and lignin biosynthesis was a downstream branch of the phenylpropane metabolic pathway [34,35]. Studies have shown that exogenous MT is involved in lignin biosynthesis. Li et al. [36] reported that the exogenous MT enhanced the resistance of cotton to verticillium wilt by up-regulating the expression of lignin and gossypol synthesis-related genes in the phenylpropane metabolic pathway, mevalonic acid pathway, and gossypol synthesis pathway. Qu et al. [37] found that the lignin contents of blueberry fruit were promoted by increasing the activities of PAL, C4H, 4CL, CAD, PPO, and POD after soaking in the exogenous MT solution. In this study, we measured the lignin contents of oriental melon scion and squash rootstock after the exogenous MT treatment and found that the lignin contents were significantly increased (Figure 1A) by increasing the related enzyme (HTC, HCALDH, COMT, CCoAOMT, PAL, CAD) activities (Figure 1B–H). The results were similar to those of Li et al. [36] and Qu et al. [37]. However, it remains unclear whether the increase in lignin content in the oriental melon scion stem will promote the graft union healing of oriental melon grafted onto squash rootstock. Some reports indicated that the success of plant grafting depended on the effective connection of the vascular bundle between the scion and rootstock [38,39]. We found that the exogenous MT treatment accelerated the graft union healing process through the acid fuchsin absorption and paraffin section tests (Figure 2 and Figure 3). This suggested that exogenous MT treatment is beneficial for the graft union healing of oriental melon grafted onto squash rootstock. Cinnamyl alcohol dehydrogenase (CAD) is a vital enzyme function at the last step in the lignin synthesis, and jasmonic acid (JA) increased the expression levels of CmCADs to regulate the lignin deposition in the melon stems [40]. In this study, the exogenous MT treatment could significantly increase the CmCAD1 expression (Figure 6A), and the graft union healing process was delayed after the CmCAD1 silencing in the oriental melon stems (Figure 7 and Figure 8). The results indicated that the positive influence of exogenous MT-induced lignin deposition was advantageous for the graft union healing process of oriental melon scion grafted onto squash rootstock. Nevertheless, further investigation requires a comprehensive understanding of the internal regulatory mechanisms governed by exogenous MT treatment. Exploring these intricacies will contribute to a more nuanced comprehension of how exogenous MT actively participated in and regulated the graft union healing, paving the way for potential applications in optimizing and enhancing this essential process in plants.
The plant hormones IAA, CTK, and GAs, were closely related to callus formation, vascular bundle development, and reconnection during the graft union healing process [41,42,43]. Some reports showed that applying exogenous naphthylacetic acid (NAA) could significantly promote graft union formation [44]. It has been reported that several essential genes play a role in regulating graft union healing. WIND1 regulates the callus formation at the grafted junction [24,45]. WOX4 regulates the vascular cambium development [46]. CDKB1;2 may promote cell cycle progression [47]. TMO6 regulates the vascular and cell-wall-related gene expression at the graft junction [31]. VND7 promotes xylem vessel cell differentiation [32,33]. To investigate whether the exogenous MT treatment affected the expression of genes related to graft union healing, we analyzed the expression characteristics of CmWIND1 and CmoWIND1, CmWOX4 and CmoWOX4, CmCDKB1;2 and CmoCDKB1;2, CmTMO6 and CmoTMO6, and CmVND7 and CmoVND7 at different days after grafting (Figure 4 and Figure 5). The results indicate that exogenous MT treatment significantly enhanced the expression of CmWIND1 and CmoWIND1, with a notably pronounced effect on the rootstock. Additionally, the expression level of CmoWOX4 was significantly higher than that of the control at 1 DAG, although it did not significantly affect CmWOX4. At 6 DAG, the expression levels of CmCDKB1;2 and CmoCDKB1;2 and CmTMO6 and CmoTMO6 were significantly higher than those of the control. Furthermore, the expression levels of CmVND7 and CmoVND7 were notably higher than those of the control at 8 DAG. So, exogenous MT treatment could accelerate graft union healing of oriental melon scion grafted onto squash rootstock by increasing the expression levels of genes related to graft union healing. In addition, Chen et al. [7] showed that MT was also involved in regulating plant root growth, and the mustard seedlings treated with low MT concentration could promote their root growth. So, we analyzed the grafted seedlings’ quality after the exogenous MT treatment and found that the root length, root surface area, root average diameter, and the total number of root tips of grafted seedlings with exogenous MT treatment were all higher than those of the control (Figure 9). However, the molecular mechanism of applying exogenous MT to regulate the graft union healing process of oriental melon grafted onto squash rootstock remains to be further studied and clarified. This intricate process involves multiple molecular and biological mechanisms, and understanding its detailed molecular regulatory network is crucial for effectively promoting graft union healing. By delving deeper into the role of melatonin in this process, we can anticipate discovering more key genes, signaling pathways, and biochemical reactions involved, thereby gaining a more profound understanding of how to optimize and enhance plant graft union healing.

4. Materials and Methods

4.1. Plant Materials

In this study, we used the oriental melon ‘T0948-2’ cultivar (Cucumis melo var. makuwa Makino) and squash ‘ShengZhen No. 1’ cultivar (C. moschata) as the scion and rootstock, respectively. The growth conditions of the rootstock and scion seedlings consisted of 25–28 °C during day and 18–20 °C at night, substrate relative humidity of 60–70%, and 9–10 h of sunlight. The melatonin (300 µmol·L−1, MT) was sprayed every two days on the leaf surfaces of the oriental melon and squash when the cotyledon was unfolded, and distilled water was sprayed as the control. When the oriental melon scion grew to one-leaf size, the one-cotyledon graft method was used to graft [48]. The stem tissues of grafted seedlings showing the same growth characteristics were collected at 2, 5, 6, 8, and 9 days after grafting (DAG). The collected samples were immediately transferred to liquid nitrogen and stored at −80 °C. Three bio-replicates were prepared for each treatment.

4.2. Determination of Lignin Content and Enzyme Activities

We sampled 0.5 g of stem tissues from the graft junction to measure the lignin contents of grafted seedlings [49], and the enzyme activities related to lignin synthesis were also measured. The CAD and 4CL activities were determined according to Takshak et al. [50], and the PAL activity was measured according to Su et al. [51]. According to the enzyme-linked immunosorbent assay (ELISA) kit (Jiangsu Meimian Industrial Co., Ltd., Yancheng, China) manual, the other enzyme activities (HCT, HCALDH, COMT, CCoAOMT) were also measured. Three separate biological experiments were conducted under the same conditions to replicate results.

4.3. Histological Section Observation

The 0.3–0.5cm stems above and below the graft junction of grafted seedlings were sampled. The samples were fixed, softened, dehydrated, infiltrated, and embedded in paraffin, according to Ribeiro et al. [52]. Transverse serial sections approximately 10 μm thick were cut and stained with pH 4.4 toluidine blue [53] and mounted using synthetic resin (Permount). Sections were examined using a light microscope (Lecia RM 2245, Nussloch, Germany). The acid fuchsin absorption assay was also conducted to identify the scion and rootstock connection. We randomly selected five plants, respectively, from thirty plants in the MT treatment and control. The 1.0 cm stem segments above and below the graft junction were cross-cut, the rootstock stems were vertically placed in 1% acidic fuchsin solution for 1 h, and then the 2.5 mm stem segments above the graft union were cross-cut to investigate the acid fuchsin absorption. The acid fuchsin absorption was observed and photographed under a confocal laser microscope.

4.4. Quantitative Real-Time PCR (qRT-PCR)

We used qRT-PCR to determine the relative expression of CmWIND1 and CmoWIND1, Cm CDKB1;2 and Cmo CDKB1;2, CmTMO6 and CmoTMO6, CmVND7 and CmoVND7, and CmCADs (CmCAD1, CmCAD2, CmCAD3, CmCAD4) in the stem tissues of oriental melon and squash rootstock. The qRT-PCR was conducted using a Bio-Rad CFX96 PCR machine and Pro Taq HS SYBR Green premix qPCR kit (AG) in a 20 μL reaction system. The components of the system included 2× SYBR Green Pro Taq HS Premix (10 μL), cDNA (2 μL), forward and reverse primers (0.4 μL each), and ddH2O (7.2 μL). The thermal cycling protocol was initial denaturation at 95 °C for 2 min, followed by 40 cycles of 10 s at 95 °C and 30 s at 60 °C [54]. Three separate biological experiments were conducted under the same conditions to replicate the results.

4.5. Virus-Induced Gene Silencing (VIGS) Assay

The CmCAD1 gene was amplified by PCR and cloned into the pTRV2 vector. Subsequently, the TRV2-CmCAD1 silencing vector was constructed, and pTRV1, pTRV2, and TRV2-CmCAD1 were transformed into the Agrobacterium EHA105 receptor state [55]. The pTRV1, pTRV2, and TRV2-CmCAD1 were suspended to OD600 = 1.0. Upon exposure to the core, the oriental melon scion seedlings were injected with an infectious liquid via a syringe into the cotyledon. TRV1 and TRV2-CmCAD1 were blended in a 1:1 ratio, and the combination of TRV1 and TRV2 was then injected into the back side of the oriental melon scions’ cotyledons. TRV-CmCAD1 and TRV-Control oriental melon lines were obtained. After the injection, the oriental melon scion seedlings were cultured in the artificial light incubator, then in darkness for 18 h, followed by normal day–night alternation. The light temperature was 26 °C, and the dark temperature was 18 °C. The graft was conducted during the one-leaf unfolding. In the graft union healing process, we sampled the stem tissues of the oriental melon scion to measure the relative expression of CmCAD1 and analyzed the reconnection of the scion and rootstock.

4.6. Statistical Analysis

The data are presented as the mean ± standard deviation of three replicate samples and were plotted and statistically analyzed by PraphPad Prism8.0.2 software. Differences in samples were assessed at a significance level (p ≤ 0.05, p ≤ 0.01, p ≤ 0.0001) by a one-way ANOVA test.

5. Conclusions

The exogenous MT application significantly increased the enzyme activities related to lignin synthesis and lignin content in the oriental melon scion and squash rootstock stems. Moreover, the lignin accumulation induced by the exogenous MT significantly promoted the graft union healing of oriental melon scion grafted onto squash rootstock and improved the qualities of grafted seedlings.

Author Contributions

Y.Z. (Yulei Zhu) and J.G.: investigation, data curation, validation, software, writing—original draft; F.W.: investigation, software; H.Y., J.M., Y.Z. (Yingtong Zhao) and Y.L.: investigation; C.T.: validation; C.X.: project administration, supervision, writing—review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Key R&D Program of China (2023YFD2300700), the National Natural Science Foundation of China (32272696), and Department of Science & Technology of Liaoning province (2023JH1/10200010).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Louws, F.J.; Rivard, C.L.; Kubota, C. Grafting fruiting vegetables to manage soilborne pathogens, foliar pathogens, arthropods and weeds. Sci. Hortic. 2010, 127, 127–146. [Google Scholar] [CrossRef]
  2. Lu, X.; Liu, W.; Wang, T.; Zhang, J.; Li, X.; Zhang, W. Systemic Long-Distance Signaling and Communication Between Rootstock and Scion in Grafted Vegetables. Front. Plant Sci. 2020, 11, 460. [Google Scholar] [CrossRef] [PubMed]
  3. Moore, R. Studies of vegetative compatibility-incompatibility in higher plants. IV. The development of tensile strength in a compatible and an incompatible graft. Protoplasma 1983, 115, 114–121. [Google Scholar] [CrossRef]
  4. Tan, D.X.; Manchester, L.C.; Terron, M.P.; Flores, L.J.; Reiter, R.J. One molecule, many derivatives: A never-ending interaction of melatonin with reactive oxygen and nitrogen species? J. Pineal Res. 2007, 42, 28–42. [Google Scholar] [CrossRef]
  5. Fazal, H.; Abbasi, B.H.; Ahmad, N.; Ali, M. Exogenous melatonin trigger biomass accumulation and production of stress enzymes during callogenesis in medicinally important Prunella vulgaris L. (Selfheal). Physiol. Mol. Biol. Plants 2018, 24, 1307–1315. [Google Scholar] [CrossRef] [PubMed]
  6. Deng, B.; Yang, K.; Zhang, Y.; Li, Z. Can antioxidant’s reactive oxygen species (ROS) scavenging capacity contribute to aged seed recovery? Contrasting effect of melatonin, ascorbate and glutathione on germination ability of aged maize seeds. Free Radic. Res. 2017, 51, 765–771. [Google Scholar] [CrossRef]
  7. Chen, Q.; Qi, W.B.; Reiter, R.J.; Wei, W.; Wang, B.M. Exogenously applied melatonin stimulates root growth and raises endogenous indoleacetic acid in roots of etiolated seedlings of Brassica juncea. J. Plant Physiol. 2009, 166, 324–328. [Google Scholar] [CrossRef]
  8. Zhang, Z.; Wang, T.; Liu, G.; Hu, M.; Yun, Z.; Duan, X.; Cai, K.; Jiang, G. Inhibition of downy blight and enhancement of resistance in litchi fruit by postharvest application of melatonin. Food Chem. 2021, 347, 129009. [Google Scholar] [CrossRef]
  9. Shi, H.; Tan, D.X.; Reiter, R.J.; Ye, T.; Yang, F.; Chan, Z. Melatonin induces class A1 heat-shock factors (HSFA1s) and their possible involvement of thermotolerance in Arabidopsis. J. Pineal Res. 2015, 58, 335–342. [Google Scholar] [CrossRef]
  10. Wang, P.; Sun, X.; Li, C.; Wei, Z.; Liang, D.; Ma, F. Long-term exogenous application of melatonin delays drought-induced leaf senescence in apple. J. Pineal Res. 2013, 54, 292–302. [Google Scholar] [CrossRef]
  11. Uchendu, E.E.; Shukla, M.R.; Reed, B.M.; Saxena, P.K. Melatonin enhances the recovery of cryopreserved shoot tips of American elm (Ulmus americana L.). J. Pineal Res. 2013, 55, 435–442. [Google Scholar] [CrossRef] [PubMed]
  12. Yin, L.; Wang, P.; Li, M.; Ke, X.; Li, C.; Liang, D.; Wu, S.; Ma, X.; Li, C.; Zou, Y.; et al. Exogenous melatonin improves Malus resistance to Marssonina apple blotch. J. Pineal Res. 2013, 54, 426–434. [Google Scholar] [CrossRef] [PubMed]
  13. Zhao, Y.; Qi, L.W.; Wang, W.M.; Saxena, P.K.; Liu, C.Z. Melatonin improves the survival of cryopreserved callus of Rhodiola crenulata. J. Pineal Res. 2011, 50, 83–88. [Google Scholar] [CrossRef] [PubMed]
  14. Zhao, D.Q.; Luan, Y.T.; Shi, W.B.; Tang, Y.H.; Huang, X.Q.; Tao, J. Melatonin enhances stem strength by increasing lignin content and secondary cell wall thickness in herbaceous peony. J. Exp. Bot. 2022, 73, 5974–5991. [Google Scholar] [CrossRef] [PubMed]
  15. Hou, J.N.; Zhao, F.A.; Yang, X.J.; Li, W.; Xie, D.Y.; Tang, Z.J.; Lv, S.P.; Nie, L.H.; Sun, Y.; Wang, M.M.; et al. Lignin synthesis related genes with potential significance in the response of upland cotton to Fusarium wilt identified by transcriptome profiling. Trop. Plant Biol. 2021, 14, 106–119. [Google Scholar] [CrossRef]
  16. Han, M.H.; Yang, N.; Wan, Q.W.; Teng, R.M.; Duan, A.Q.; Wang, Y.H.; Zhuang, J. Exogenous melatonin positively regulates lignin biosynthesis in Camellia sinensis. Int. J. Biol. Macromol. 2021, 179, 485–499. [Google Scholar] [CrossRef]
  17. Moura, J.C.M.S.; Bonine, C.A.V.; Viana, J.D.O.F.; Dornelas, M.C.; Mazzafera, P. Abiotic and biotic stresses and changes in the lignin content and composition in plants. J. Integr. Plant Biol. 2010, 52, 360–376. [Google Scholar] [CrossRef] [PubMed]
  18. Derikvand, M.M.; Sierra, J.B.; Ruel, K.; Pollet, B.; Do, C.T.; Thévenin, J.; Buffard, D.; Jouanin, L.; Lapierre, C. Redirection of the phenylpropanoid pathway to feruloyl malate in Arabidopsis mutants deficient for cinnamoyl-CoA reductase 1. Planta 2008, 227, 943–956. [Google Scholar] [CrossRef]
  19. Rest, B.V.D.; Rochange, S.F. Down-regulation of cinnamoyl-CoA reductase in tomato (Solanum lycopersicum L.) induces dramatic changes in soluble phenolic pools. J. Exp. Bot. 2006, 57, 1399–1411. [Google Scholar] [CrossRef]
  20. Tripathi, S.C.; Sayre, K.D.; Kaul, J.N.; Narang, R.S. Growth and morphology of spring wheat (Triticum aestivum L.) culms and their association with lodging: Effects of genotypes, N levels and ethephon. Field Crops Res. 2003, 84, 271–290. [Google Scholar] [CrossRef]
  21. Xu, C.Q.; Zhang, Y.; Zhao, M.Z.; Liu, Y.; Xu, X.; Li, T.L. Transcriptomic analysis of melon/squash graft junction reveals molecular mechanisms potentially underlying the graft union development. Peer J. 2021, 9, e12569. [Google Scholar] [CrossRef] [PubMed]
  22. Chen, Z.; Zhao, C.; Hu, F.; Qin, Y.; Wang, X.; Hu, G. Transcriptome changes between compatible and in compatible graft combination of Litchi chinensis by digital gene expression profile. Sci. Rep. 2017, 7, 3954. [Google Scholar] [CrossRef] [PubMed]
  23. Cookson, S.J.; Clemente Moreno, M.J.; Hevin, C.; Nyamba Mendome, L.Z.; Delrot, S.; Trossat-Magnin, C.; Ollat, N. Graft union formation in grapevine induces transcriptional changes related to cell wall modification, wounding, hormone signaling, and secondary metabolism. J. Exp. Bot. 2013, 64, 2997–3008. [Google Scholar] [CrossRef] [PubMed]
  24. Melnyk, C.W.; Meyerowitz, E.M. Plant grafting. Curr. Biol. 2015, 25, 183–188. [Google Scholar] [CrossRef] [PubMed]
  25. Ikeuchi, M.; Sugimoto, K.; Iwase, A. Plant callus: Mechanisms of induction and repression. Plant Cell 2013, 25, 3159–3173. [Google Scholar] [CrossRef]
  26. Tanaka, W.; Hirano, H.Y. Antagonistic action of TILLERS ABSENT1 and FLORAL ORGAN NUMBER2 regulates stem cell maintenance during axillary meristem development in rice. New Phytol. 2020, 2, 974–984. [Google Scholar] [CrossRef] [PubMed]
  27. Zhang, Y.; Jiao, Y.; Jiao, H.; Zhao, H.; Zhu, Y.X. Two-Step Functional Innovation of the Stem-Cell Factors WUS/WOX5 during Plant Evolution. Mol. Biol. Evol. 2017, 34, 640–653. [Google Scholar] [CrossRef] [PubMed]
  28. Hirakawa, Y.; Kondo, Y.; Fukuda, H. TDIF peptide signaling regulates vascular stem cell proliferation via the WOX4 homeobox gene in Arabidopsis. Plant Cell 2010, 22, 2618–2629. [Google Scholar] [CrossRef]
  29. Haecker, A.; Gross-Hardt, R.; Geiges, B.; Sarkar, A.; Breuninger, H.; Herrmann, M.; Laux, T. Expression dynamics of WOX genes mark cell fate decisions during early embryonic patterning in Arabidopsis thaliana. Development 2004, 131, 657–668. [Google Scholar] [CrossRef]
  30. Thomas, H.; Van den Broeck, L.; Spurney, R.; Sozzani, R.; Frank, M. Gene regulatory networks for compatible versus incompatible grafts identify a role for SlWOX4 during junction formation. Plant Cell 2022, 34, 535–556. [Google Scholar] [CrossRef]
  31. Zhang, A.; Matsuoka, K.; Kareem, A.; Robert, M.; Roszak, P.; Blob, B.; Anchal Bisht, A.; De Veylder, L.; Voiniciuc, C.; Asahina, M.; et al. Cell-wall damage activates DOF transcription factors to promote wound healing and tissue regeneration in Arabidopsis thaliana. Curr. Biol. 2022, 32, 1883–1894. [Google Scholar] [CrossRef]
  32. Tan, T.T.; Endo, H.; Sano, R.; Kurata, T.; Yamaguchi, M.; Ohtani, M.; Demura, T. Transcription Factors VND1-VND3 Contribute to Cotyledon Xylem Vessel Formation. Plant Physiol. 2018, 176, 773–789. [Google Scholar] [CrossRef]
  33. Kubo, M.; Udagawa, M.; Nishikubo, N.; Horiguchi, G.; Yamaguchi, M.; Ito, J.; Tetsuro, M.; Hiroo, F.; Taku, D. Transcription switches for protoxylem and metaxylem vessel formation. Genes. Dev. 2005, 19, 1855–1860. [Google Scholar] [CrossRef]
  34. Cass, C.L.; Peraldi, A.; Dowd, P.F.; Mottiar, Y.; Santoro, N.; Karlen, S.D.; Bukhman, Y.V.; Foster, C.E.; Thrower, N.; Bruno, L.C.; et al. Effects of PHENYLALANINE AMMONIA LYASE (PAL) knockdown on cell wall composition, biomass digestibility, and biotic and abiotic stress responses in Brachypodium. J. Exp. Bot. 2015, 66, 4317–4335. [Google Scholar] [CrossRef] [PubMed]
  35. La Camera, S.; Gouzerh, G.; Dhondt, S.; Hoffmann, L.; Fritig, B.; Legrand, M.; Heitz, T. Metabolic reprogramming in plant innate immunity: The contributions of phenylpropanoid and oxylipin pathways. Immunol. Rev. 2004, 198, 267–284. [Google Scholar] [CrossRef]
  36. Li, C.; He, Q.; Zhang, F.; Yu, J.; Li, C.; Zhao, T.; Zhang, Y.; Xie, Q.; Su, B.; Mei, L.; et al. Melatonin enhances cotton immunity to Verticillium wilt via manipulating lignin and gossypol biosynthesis. Plant J. 2019, 100, 784–800. [Google Scholar] [CrossRef]
  37. Qu, G.F.; Wu, W.N.; Ba, L.J.; Ma, C.; Ji, N.; Cao, S. Melatonin Enhances the Postharvest Disease Resistance of Buleberries Fruit by Modulaing the Jasmonic Acid Signaling Pathway and Phenylpropanoid Metabolites. Front. Chem. 2022, 10, 957581. [Google Scholar] [CrossRef] [PubMed]
  38. Pina, A.; Cookson, S.J.; Calatayud, A.; Trinchera, A.; Errea, P. Physiological and molecular mechanisms underlying graft compatibility. In Vegetable Grafting Principles and Practices; Colla, G., Perez Alfocea, F., Schwarz, D., Eds.; CABI: Wallingford, UK, 2017. [Google Scholar]
  39. Yang, Z.J.; Feng, J.L.; Chen, H. Study on the Anatomical Structures in Development of the Nurse Seed Grafted Union of Camellia oleifera. Plant Sci. J. 2013, 31, 313–320. [Google Scholar] [CrossRef]
  40. Liu, W.; Jiang, Y.; Jin, Y.Z.; Wang, C.H.; Yang, J.; Qi, H.Y. Drought-induced ABA, H2O2 and JA positively regulate CmCAD genes and lignin synthesis in melon stems. BMC Plant Biol. 2021, 21, 83. [Google Scholar] [CrossRef] [PubMed]
  41. Bishopp, A.; Help, H.; El-Showk, S.; Weijers, D.; Scheres, B.; Friml, J.; Benková, E.; Mähönen, A.P.; Helariuttam, Y. A mutually inhibitory interaction between auxin and cytokinin specifies vascular pattern in roots. Curr. Biol. 2011, 21, 917–926. [Google Scholar] [CrossRef]
  42. Mauriat, M.; Moritz, T. Analyses of GA20ox- and GID1-over-expressing aspen suggest that gibberellins play two distinct roles in wood formation. Plant J. 2009, 58, 989–1003. [Google Scholar] [CrossRef] [PubMed]
  43. Nieminen, K.; Immanen, J.; Laxell, M.; Kauppinen, L.; Tarkowski, P.; Dolezal, K.; Tähtiharju, S.; Elo, A.; Decourteix, M.; Ljung, K. Cytokinin signaling regulates cambial development in poplar. Proc. Natl. Acad. Sci. USA 2008, 105, 20032–20037. [Google Scholar] [CrossRef] [PubMed]
  44. Xu, C.Q.; Wu, F.; Guo, J.Y.; Hou, S.A.; Wu, X.F.; Xin, Y. Transcriptomic analysis and physiological characteristics of exogenous naphthylacetic acid application to regulate the healing process of oriental melon grafted onto squash. Peer J. 2022, 10, e13980. [Google Scholar] [CrossRef] [PubMed]
  45. Iwase, A.; Mitsuda, N.; Koyama, T.; Hiratsu, K.; Kojima, M.; Arai, T.; Inoue, Y.; Seki, M.; Sakakibara, H.; Sugimoto, K.; et al. The AP2/ERF transcription factor WIND1 controls cell dedifferentiation in Arabidopsis. Curr. Biol. 2011, 21, 508–514. [Google Scholar] [CrossRef]
  46. Zhang, J.; Eswaran, G.; Alonso-Serra, J.; Kucukoglu, M.; Xiang, J.L.; Yang, W.B.; Elo, A.; Nieminen, K.; Damén, T.; Joung, J.G.; et al. Transcriptional regulatory framework for vascular cambium development in Arabidopsis roots. Nat. Plants 2019, 5, 1033–1042. [Google Scholar] [CrossRef] [PubMed]
  47. Van Leene, J.; Hollunder, J.; Eeckhout, D.; Persiau, G.; Van De Slijke, E.; Stals, H.; Van Isterdale, G.; Verkest, A.; Neirynck, S.; Buffel, Y.; et al. Targeted interactomics reveals a complex core cell cycle machinery in Arabidopsis thaliana. Mol. Syst. Biol. 2010, 6, 397. [Google Scholar] [CrossRef] [PubMed]
  48. Davis, A.R.; Perkins-Veazie, P.; Sakata, Y.; Lopez-Galarza, S.; Maroto, J.V.; Lee, S.G.; Huh, Y.C.; Sun, Z.Y.; Migule, A.; King, S.R.; et al. Cucurbit grafting. Crit. Rev. Plant Sci. 2008, 27, 50–74. [Google Scholar] [CrossRef]
  49. Zhang, L.B.; Wang, G.; Chang, J.M.; Liu, J.S.; Cai, J.H.; Rao, X.W.; Zhang, L.J.; Zhong, J.J.; Xie, J.H.; Zhu, S.J. Effects of 1-MCP and ethylene on expression of three CAD genes and lignification in stems of harvested Tsai Tai (Brassica chinensis). Food Chem. 2010, 123, 32–40. [Google Scholar] [CrossRef]
  50. Takshak, S.; Agrawal, S.B. Secondary metabolites and phenylpropanoid pathway enzymes as influenced under supplemental ultraviolet-B radiation in Withania somnifera Dunal, an indigenous medicinal plant. J. Photochem. Photobiol. B Biol. 2014, 140, 332–343. [Google Scholar] [CrossRef] [PubMed]
  51. Su, J.; Tu, K.; Cheng, L.; Tu, S.C.; Wang, M.; Xu, H.R.; Zhan, G. Wound-induced H2O2 and resistance to Botrytis cinerea decline with the ripening of apple fruit. Postharvest Biol. Technol. 2011, 62, 64–70. [Google Scholar] [CrossRef]
  52. Ribeiro, L.M.; Nery, L.A.; Vieira, L.M.; Mercadante-Simões, M.O. Histological study of micrografting in passionfruit. Plant Cell Tissue Organ Cult. (PCTOC) 2015, 123, 173–181. [Google Scholar] [CrossRef]
  53. O’Brien, T.P.; Feder, N.; McCully, M.E. Polychromatic staining of plant cell walls by toluidine blue O. Protoplasma 1964, 59, 368–373. [Google Scholar] [CrossRef]
  54. Hou, S.A.; Zhu, Y.L.; Wu, X.F.; Xin, Y.; Guo, J.Y.; Wu, F.; Yu, H.Q.; Sun, Z.Q.; Xu, C.Q. Scion-to-Rootstock Mobile Transcription Factor CmHY5 Positively Modulates the Nitrate Uptake Capacity of Melon Scion Grafted on Squash Rootstock. Int. J. Mol. Sci. 2023, 24, 162. [Google Scholar] [CrossRef] [PubMed]
  55. Wu, K.; Wu, Y.; Zhang, C.; Fu, Y.; Liu, Z.; Zhang, X. Simultaneous silencing of two different Arabidopsis genes with a novel virus-induced gene silencing vector. Plant Methods 2021, 17, 6. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Effects of exogenous MT application on lignin content and enzyme activities related to lignin biosynthesis of oriental melon and squash seedling stems ((A), lignin content. (B), HCT activities. (C), HCALDH activities. (D), COMT activities. (E), CCoAOMT activities. (F), PAL activities. (G), 4CL activities. (H), CAD activities. MT, melatonin. ns, no significance. *, p ≤ 0.05. **, p ≤ 0.01. ***, p ≤ 0.001. ****, p ≤ 0.0001).
Figure 1. Effects of exogenous MT application on lignin content and enzyme activities related to lignin biosynthesis of oriental melon and squash seedling stems ((A), lignin content. (B), HCT activities. (C), HCALDH activities. (D), COMT activities. (E), CCoAOMT activities. (F), PAL activities. (G), 4CL activities. (H), CAD activities. MT, melatonin. ns, no significance. *, p ≤ 0.05. **, p ≤ 0.01. ***, p ≤ 0.001. ****, p ≤ 0.0001).
Ijms 25 03690 g001
Figure 2. Observation of acid fuchsin absorption during the graft healing process of oriental melon scion grafted onto squash rootstock (MT, melatonin. DAG, days after grafting. Scale bars, 1 mm).
Figure 2. Observation of acid fuchsin absorption during the graft healing process of oriental melon scion grafted onto squash rootstock (MT, melatonin. DAG, days after grafting. Scale bars, 1 mm).
Ijms 25 03690 g002
Figure 3. Paraffin section observation during the graft healing process of oriental melon scion grafted onto squash rootstock (IL, the isolated layer. CA, the callus. VB, the vascular bundles. Sc, scion. Rt, rootstock. MT, melatonin. DAG, days after grafting. Scale bars, 150 µm).
Figure 3. Paraffin section observation during the graft healing process of oriental melon scion grafted onto squash rootstock (IL, the isolated layer. CA, the callus. VB, the vascular bundles. Sc, scion. Rt, rootstock. MT, melatonin. DAG, days after grafting. Scale bars, 150 µm).
Ijms 25 03690 g003
Figure 4. The relative expression of genes related to graft union healing in the oriental melon scion during the graft healing process ((A), CmWIND1. (B), CmWOX4. (C), CmCDKB1;2. (D), CmTMO6. (E), CmVND7. MT, melatonin. NG, no grafting. DAG, days after grafting. Different letters indicate significant differences, p ≤ 0.05).
Figure 4. The relative expression of genes related to graft union healing in the oriental melon scion during the graft healing process ((A), CmWIND1. (B), CmWOX4. (C), CmCDKB1;2. (D), CmTMO6. (E), CmVND7. MT, melatonin. NG, no grafting. DAG, days after grafting. Different letters indicate significant differences, p ≤ 0.05).
Ijms 25 03690 g004
Figure 5. The relative expression of genes related to graft union healing in the squash rootstock during the graft healing process ((A), CmoWIND1. (B), CmoWOX4. (C), CmoCCDKB1;2. (D), CmoTMO6. (E), CmoVND7. MT, melatonin. NG, no grafting. DAG, days after grafting. Different letters indicate significant differences, p ≤ 0.05).
Figure 5. The relative expression of genes related to graft union healing in the squash rootstock during the graft healing process ((A), CmoWIND1. (B), CmoWOX4. (C), CmoCCDKB1;2. (D), CmoTMO6. (E), CmoVND7. MT, melatonin. NG, no grafting. DAG, days after grafting. Different letters indicate significant differences, p ≤ 0.05).
Ijms 25 03690 g005
Figure 6. The relative expression of CmCADs in the oriental melon scion during the graft healing process ((A), CmCAD1. (B), CmCAD2. (C), CmCAD3. (D), CmCAD4. MT, melatonin. DAG, days after grafting. Different letters indicate significant differences, p ≤ 0.05).
Figure 6. The relative expression of CmCADs in the oriental melon scion during the graft healing process ((A), CmCAD1. (B), CmCAD2. (C), CmCAD3. (D), CmCAD4. MT, melatonin. DAG, days after grafting. Different letters indicate significant differences, p ≤ 0.05).
Ijms 25 03690 g006
Figure 7. The relative expression of CmCAD1 and lignin content of oriental melon scion stem after the transiently silenced CmCAD1 during the graft healing process ((A), lignin content. (B), the relative expression levels of CmCAD1. DAG, days after grafting. Different letters indicate significant differences, **, p ≤ 0.01. ****, p ≤ 0.0001).
Figure 7. The relative expression of CmCAD1 and lignin content of oriental melon scion stem after the transiently silenced CmCAD1 during the graft healing process ((A), lignin content. (B), the relative expression levels of CmCAD1. DAG, days after grafting. Different letters indicate significant differences, **, p ≤ 0.01. ****, p ≤ 0.0001).
Ijms 25 03690 g007
Figure 8. Observation of acid fuchsin absorption after the transiently silenced CmCAD1 during the graft union healing process of oriental melon scion grafted onto squash rootstock (DAG, days after grafting. Scale bars, 1 mm).
Figure 8. Observation of acid fuchsin absorption after the transiently silenced CmCAD1 during the graft union healing process of oriental melon scion grafted onto squash rootstock (DAG, days after grafting. Scale bars, 1 mm).
Ijms 25 03690 g008
Figure 9. Analysis of root growth characteristics of five-leaf grafted seedlings treated with the exogenous MT ((A), photographs of roots. (B), root length. (C), root surface area. (D), root average diameter. (E), the total number of root tips. (F), the total number of root forks. MT, melatonin. Different letters indicate significant differences, p ≤ 0.05).
Figure 9. Analysis of root growth characteristics of five-leaf grafted seedlings treated with the exogenous MT ((A), photographs of roots. (B), root length. (C), root surface area. (D), root average diameter. (E), the total number of root tips. (F), the total number of root forks. MT, melatonin. Different letters indicate significant differences, p ≤ 0.05).
Ijms 25 03690 g009
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Zhu, Y.; Guo, J.; Wu, F.; Yu, H.; Min, J.; Zhao, Y.; Tan, C.; Liu, Y.; Xu, C. Exogenous Melatonin Application Accelerated the Healing Process of Oriental Melon Grafted onto Squash by Promoting Lignin Accumulation. Int. J. Mol. Sci. 2024, 25, 3690. https://doi.org/10.3390/ijms25073690

AMA Style

Zhu Y, Guo J, Wu F, Yu H, Min J, Zhao Y, Tan C, Liu Y, Xu C. Exogenous Melatonin Application Accelerated the Healing Process of Oriental Melon Grafted onto Squash by Promoting Lignin Accumulation. International Journal of Molecular Sciences. 2024; 25(7):3690. https://doi.org/10.3390/ijms25073690

Chicago/Turabian Style

Zhu, Yulei, Jieying Guo, Fang Wu, Hanqi Yu, Jiahuan Min, Yingtong Zhao, Changhua Tan, Yuanwei Liu, and Chuanqiang Xu. 2024. "Exogenous Melatonin Application Accelerated the Healing Process of Oriental Melon Grafted onto Squash by Promoting Lignin Accumulation" International Journal of Molecular Sciences 25, no. 7: 3690. https://doi.org/10.3390/ijms25073690

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop