Multi-omics analyses reveal the effects of layerage and grafting on flavonoid synthesis and accumulation in Citrus reticulata ‘Chachi’

Jianmu Su , Mingmin Jiang , Huimin Pan , Weitao Zhou , Xueyan Cai , Yukun Wang , Wei Liu , Desen Wang , Mei Bai , Hong Wu

Horticulture Research ›› 2025, Vol. 12 ›› Issue (10) : 177

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Horticulture Research ›› 2025, Vol. 12 ›› Issue (10) :177 DOI: 10.1093/hr/uhaf177
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Multi-omics analyses reveal the effects of layerage and grafting on flavonoid synthesis and accumulation in Citrus reticulata ‘Chachi’

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Abstract

Guangdong Citri Reticulatae Pericarpium from the dry and mature peel of Citrus reticulata ‘Chachi’ (CRC) is a well-known medicinal and food material in Asia. The main propagation methods of CRC are layerage and grafting. It is generally considered that the quality of CRC from layerage is superior to that obtained from plants propagated by grafting. Nevertheless, the effects of layerage and grafting on the biosynthesis of flavonoid (main bioactive ingredients) in the peel of CRC remain unknown. Here, metabolomic analyses revealed the effects of layerage, self-grafting, and heterografting (Citrus limonia as rootstock) on flavonoid biosynthesis in CRC from two main harvesting periods, CRCV (Citri Reticulatae Chachiensis Viride) and CRCR (Citri Reticulatae Chachiensis Reddish). Compared with CRCR, CRCV exhibited a higher content of flavonoids. Grafting CRC onto C. limonia exhibited a higher content of hesperidin, nobiletin, tangeretin, narirutin, demethylnobiletin, and sinensetin than layerage and self-grafting. This increase can be attributed to the upregulation of genes involved in flavonoid synthesis. Further, the transcription factor CrcMYBF1 was identified within the gene coexpression network and is confirmed to be significantly induced by methyl jasmonate (MeJA) and upregulate the expression of Crc1,6RhaT through interacting with its promoter region, thereby boosting the biosynthesis and accumulation of hesperidin. In summary, our findings provide mechanistic insights into the coordinated regulation of hesperidin biosynthesis via MeJA-inducing CrcMYBF1 in CRC. Our study is expected to provide a theoretical basis for CRC propagation and cultivation.

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Jianmu Su, Mingmin Jiang, Huimin Pan, Weitao Zhou, Xueyan Cai, Yukun Wang, Wei Liu, Desen Wang, Mei Bai, Hong Wu. Multi-omics analyses reveal the effects of layerage and grafting on flavonoid synthesis and accumulation in Citrus reticulata ‘Chachi’. Horticulture Research, 2025, 12(10): 177 DOI:10.1093/hr/uhaf177

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Acknowledgements

This work was supported by the Open Competition Program of Ten Major Directions of Agricultural Science and Technology Innovation for the 14th Five-Year Plan of Guangdong Province (2022SDZG07 to H.W.), the Key Realm R&D Program of Guangdong Province (2020B020221001 to H.W.) and the Guangdong Provincial Special Fund for Modern Agriculture Industry Technology Innovation Teams (2019KJ125 to H.W.).

Author contributions

Design and supervision: H.W. Material collection and Experiment: J.M.S., M.M.J., H.M.P., W.T.Z., X.Y.C., and D.S.W. Data analysis and visualization: J.M.S., M.M.J., Y.K.W., W.L., M.B., and H.W. Writing: J.M.S., H.M.P., and H.W.

Data availability

All raw data were deposited in the GenBank NCBI Short Read Archive under accession number PRJNA03126.

Conflict of interest statement

The authors declare no conflicts of interest.

Supplementary data

Supplementary data is available at Horticulture Research online.

References

[1]

Chinese Pharmacopoeia Commission. Pharmacopoeia of the People’s Republic of China. China Medical Science Press; 2020: Beijing

[2]

Liu Y, Heying E, Tanumihardjo SA. History, global distribution, and nutritional importance of citrus fruits. Compr Rev Food Sci Food Saf. 2012; 11:530-45

[3]

Su J, Wang Y, Bai M. et al. Soil conditions and the plant micro-biome boost the accumulation of monoterpenes in the fruit of Citrus reticulata ‘Chachi’. Microbiome. 2023; 61:1-22

[4]

Yu Q, Tao Y, Huang Y. et al. Aged Pericarpium Citri Reticulatae ’Chachi’ attenuates oxidative damage induced by tert-butyl hydroperoxide (t-BHP) in HepG 2cells. Foods. 2022; 11:273

[5]

Chen YY, Liang JJ, Wang DL. et al. Nobiletin as a chemopreventive natural product against cancer, a comprehensive review. Crit Rev Food Sci Nutr. 2023; 63:6309-29

[6]

Wang Y, Chen Y, Zhang H. et al. Polymethoxyflavones from cit-rus inhibited gastric cancer cell proliferation through inducing apoptosis by upregulating RARβ both in vitro and in vivo. Food Chem Toxicol. 2020; 146:111811

[7]

Sulaiman GM, Waheeb HM, Jabir MS. et al. Hesperidin loaded on gold nanoparticles as a drug delivery system for a successful biocompatible, anti-cancer, anti-inflammatory and phagocyto-sis inducer model. Sci Rep. 2020; 10:1-16

[8]

Boudries H, Loupassaki S, Ettoumi LY. et al. Chemical profile, antimicrobial and antioxidant activities of Citrus reticulata and Citrus clementina (L.) essential oils. Int Food Res J. 2017; 24:1782-92

[9]

Gao B, Chen Y, Zhang M. et al. Chemical composition, antioxi-dant and antimicrobial activity of Pericarpium Citri Reticulatae essential oil. Molecules. 2011; 16:4082-96

[10]

Wang F, Chen L, Chen H. et al. Discovery of the key active compounds in Citri Reticulatae Pericarpium (Citrus reticulata ‘Chachi’) and their therapeutic potential for the treatment of COVID-19 based on comparative metabolomics and network pharmacology. Front Pharmacol. 2022; 13:1-19

[11]

Zeng SL, Li SZ, Xiao PT. et al. Citrus polymethoxyflavones atten-uate metabolic syndrome by regulating gut microbiome and amino acid metabolism. Sci Adv. 2020;6:eaax6208

[12]

Liang S, Zhang J, Liu Y. et al. Study on flavonoids and bioactiv-ityfeaturesofpericarpofCitrus reticulata ‘Chachi’ at different harvest periods. Plants. 2022; 11:1-14

[13]

Ferreyra MLF, Serra P, Casati P. Recent advances on the roles of flavonoids as plant protective molecules after UV and high light exposure. Physiol Plant. 2021; 173:736-49

[14]

Lahari Z, van Boerdonk S, Omoboye OO. et al. Strigolactone deficiency induces jasmonate, sugar and flavonoid phytoalexin accumulation enhancing rice defense against the blast fungus Pyricularia oryzae. New Phytol. 2024; 241:827-44

[15]

Shang N, Tong P, Ye P. et al. Crc1,6RhaT is involved in the synthesis of hesperidin of the main bioactive substance in the Citrus reticulata ‘Chachi’ fruit. Hortic Plant J. 2024; 10:1321-35

[16]

Frydman A, Liberman R, Huhman DV. et al. The molecular and enzymatic basis of bitter/non-bitter flavor of citrus fruit: evolu-tion of branch-forming rhamnosyltransferases under domesti-cation. Plant J. 2013; 73:166-78

[17]

Li W, Li G, Yuan Z. et al. Illustration of the variation in the content of flavanone rutinosides in various citrus germplasms from genetic and enzymatic perspectives. Hortic Res. 2022;9:uhab017

[18]

Martínez-Alcántara B, Rodriguez-Gamir J, Martínez-Cuenca MR. et al. Relationship between hydraulic conductance and citrus dwarfing by the flying dragon rootstock (Poncirus trifoliata L. Raft var. monstruosa). Trees Struc Funct. 2013; 27:629-38

[19]

Fu L, Chai L, Ding D. et al. A novel citrus rootstock tolerant to iron deficiency in calcareous soil. J Am Soc Hortic Sci. 2016; 141:112-8

[20]

Liu XY, Li J, Liu MM. et al. Transcriptome profiling to understand the effect of citrus rootstocks on the growth of ‘Shatangju’ mandarin. PLoS One. 2017; 12:1-22

[21]

Lado J, Gambetta G, Zacarias L. Key determinants of citrus fruit quality: metabolites and main changes during maturation. Sci Hortic. 2018; 233:238-48

[22]

Sharma RM, Dubey AK, Awasthi OP. et al. Growth, yield, fruit quality and leaf nutrient status of grapefruit (Citrus paradisi Macf.): variation from rootstocks. Sci Hortic. 2016; 210:41-8

[23]

Albrecht U, McCollum G, Bowman KD. Influence of root-stock variety on Huanglongbing disease development in field-grown sweet orange (Citrus sinensis [L.] Osbeck) trees. Sci Hortic. 2012; 138:210-20

[24]

Cardeñosa V, Barros L, Barreira JCM. et al. Different citrus root-stocks present high dissimilarities in their antioxidant activity and vitamins content according to the ripening stage. JPlant Physiol. 2015; 174:124-30

[25]

Forner-Giner , Ballesta-De Los Santos M, Melgarejo P. et al. Influence of different rootstocks on fruit quality and primary and secondary metabolites content of blood oranges cultivars. Molecules. 2023; 28:4176

[26]

Tan EY, Li F, Lin X. et al. Comparative study on comprehensive quality of Xinhui chenpi by two main plant propagation tech-niques. Food Sci Nutr. 2023; 11:1104-12

[27]

Kaleem MM, Zhu P, Ateeq M. et al. Integrated multi-omics analysis provides molecular insights into flavor variation in melons grafted onto two different pumpkin rootstocks during fruit development. Hortic Plant J. 2024; 11:1181-97

[28]

Zhang S, Nie L, Zhao W. et al. Metabolomic analysis of the occurrence of bitter fruits on grafted oriental melon plants. PLoS One. 2019; 14:1-13

[29]

Zhong H, Liu Z, Zhang F. et al. Metabolomic and transcriptomic analyses reveal the effects of self-and hetero-grafting on antho-cyanin biosynthesis in grapevine. Hortic Res. 2022; 9:1-11

[30]

Li W, Zhan Q, Guan Y. et al. Heterografting enhances chrysanthe-mum resistance to Alternaria alternata via jasmonate-mediated increases in trichomes and terpenoids. JExpBot. 2024; 75:6523-41

[31]

Yang L, Machin F, Wang S. et al. Heritable transgene-free genome editing in plants by grafting of wild-type shoots to transgenic donor rootstocks. Nat Biotechnol. 2023; 41:958-67

[32]

Feng M, Augstein F, Kareem A. et al. Plant grafting: molecular mechanisms and applications. Mol Plant. 2024; 17:75-91

[33]

Liu W, Wang Q, Zhang R. et al. Rootstock-scion exchanging mRNAs participate in the pathways of amino acid and fatty acid metabolism in cucumber under early chilling stress. Hortic Res. 2022;9:uhac031

[34]

Liu W, Xiang C, Li X. et al. Identification of long-distance transmissible mRNA between scion and rootstock in cucurbit seedling Heterografts. Int J Mol Sci. 2020; 21:5253

[35]

Guo L, Yao H, Chen W. et al. Natural products of medicinal plants: biosynthesis and bioengineering in post-genomic era. Hortic Res. 2022; 9:1-20

[36]

Zheng GD, Liu MS, Chao YX. et al. Identification of lipophilic components in Citri Reticulatae Pericarpium cultivars by super-critical CO2 fluid extraction with ultra-high-performance liquid chromatography-Q Exactive Orbitrap tandem mass spectrome-try. J Sep Sci. 2020; 43:3421-40

[37]

Thomas HR, Frank MH. Connecting the pieces: uncovering the molecular basis for long-distance communication through plant grafting. New Phytol. 2019; 223:582-9

[38]

Zhang J, Zhang H, Wang P. et al. Gene expression, hormone signaling, and nutrient uptake in the root regermination of grafted watermelon plants with different pumpkin rootstocks. J Plant Growth Regul. 2023; 42:1051-66

[39]

El-Sayed SF, Abdel-Wahab A, El-Eslamboly A. et al. Application of grafting as a tool for improving morphological and physiological traits of cucumber plants grown under nethouse conditions. Plant Cell Biotech Mol Biol. 2021; 22:439-53

[40]

Kyriacou MC, Leskovar DI, Colla G. et al. Watermelon and melon fruit quality: the genotypic and agro-environmental factors implicated. Sci Hortic. 2018; 234:393-408

[41]

Rodrigues JDB, Moreira AS, Stuchi ES. et al. Huanglongbing inci-dence, canopy volume, and sprouting dynamics of ‘Valencia’ sweet orange grafted onto 16 rootstocks. Trop Plant Pathol. 2020; 45:611-9

[42]

Lana G, Modica G, Las CG. et al. Molecular insights into the effects of rootstocks on maturation of blood oranges. Horticul-turae. 2021; 7:1-16

[43]

Morales Alfaro J, Bermejo A, Navarro P. et al. Effect of root-stock on citrus fruit quality: a review. Food Rev Inter. 2023; 39: 2835-53

[44]

Tietel Z, Srivastava S, Fait A. et al. Impact of scion/rootstock reciprocal effects on metabolomics of fruit juice and phloem sap in grafted Citrus reticulata. PLoS One. 2020; 15:1-17

[45]

Peng Z, Song L, Chen M. et al. Neofunctionalization of an OMT cluster dominates polymethoxyflavone biosynthesis asso-ciated with the domestication of citrus. Proc Natl Acad Sci USA. 2024; 121:1-12

[46]

Su J, Peng T, Bai M. et al. Transcriptome and metabolome analy-ses provide insights into the flavonoid accumulation in peels of Citrus reticulata ‘Chachi’. Molecules. 2022; 27:6476

[47]

Taylor-Teeples M, Lin L, De Lucas. et al. An Arabidopsis gene regulatory network for secondary cell wall synthesis. Nature. 2015; 517:571-5

[48]

Li B, Fan R, Guo S. et al. The Arabidopsis MYB transcription fac-tor, MYB111 modulates salt responses by regulating flavonoid biosynthesis. Environ Exp Bot. 2019; 166:103807

[49]

Nabavi SM, Šamec D, Tomczyk M. et al. Flavonoid biosynthetic pathways in plants: versatile targets for metabolic engineering. Biotech Adv. 2020; 38:1-12

[50]

Wang H, Xu K, Li X. et al. A pear S1-bZIP transcription factor PpbZIP44 modulates carbohydrate metabolism, amino acid, and flavonoid accumulation in fruits. Hortic Res. 2023;10:uhad140

[51]

Hichri I, Barrieu F, Bogs J. et al. Recent advances in the transcrip-tional regulation of the flavonoid biosynthetic pathway. JExp Bot. 2011; 62:2465-83

[52]

Wang W, Wang Y, Li H. et al. Two MYB transcription factors (CsMYB2 and CsMYB26) are involved in flavonoid biosynthesis in tea plant [Camellia sinensis (L.) O. Kuntze]. BMC Plant Biol. 2018; 18:288

[53]

Jiang L, Yue M, Liu Y. et al. A novel R2R3-MYB transcription factor FaMYB5 positively regulates anthocyanin and proanthocyani-din biosynthesis in cultivated strawberries (Fragaria × ananassa). Plant Biotechnol J. 2023; 21:1140-58

[54]

Li H, Li Y, Yu J. et al. MdMYB8 is associated with flavonol biosynthesis via the activation of the MdFLS promoter in the fruits of Malus crabapple. Hortic Res. 2020; 7:19

[55]

Li Q, Yao J, Zheng W. et al. Hetero-grafting affects flavonoid biosynthesis in sweet orange ’Newhall’ (Citrus sinensis) peels: a metabolomics and transcriptomics analysis. Front Plant Sci. 2023; 14:1-15

[56]

Meng J, Wang H, Chi R. et al. The eTM-miR858-MYB62-like module regulates anthocyanin biosynthesis under low-nitrogen conditions in Malus spectabilis. New Phytol. 2023; 238:2524-44

[57]

Yang J, Wu X, Aucapiña C. et al. NtMYB12 requires for compe-tition between flavonol and (pro)anthocyanin biosynthesis in Narcissus tazetta tepals. Mol Hortic. 2023; 3:1-19

[58]

Li S, Dong Y, Li D. et al. Eggplant transcription factor SmMYB5 integrates jasmonate and light signaling during anthocyanin biosynthesis. Plant Physiol. 2024; 194:1139-65

[59]

Xie L., Wang Y., Tao Y., Chen L., Lin H., Qi Z. and Li J. Genome-wide identification and analysis of anthocyanin synthesis-related R2R3-MYB genes in Fragaria pentaphylla. BMC Genomics. 2024; 25:952

[60]

Cai XY, Chen JH, Chen JY. et al. Identification and quality eval-uation of Citrus reticulata cv. Chachiensis varieties based on SNP markers. Arab J Chem. 2023; 16:1-9

[61]

Wen B, Mei ZL, Zeng CW. et al. metaX: a flexible and com-prehensive software for processing metabolomics data. BMC Bioinformatics. 2017; 18:1-14

[62]

Pan H, Su J, Bai M. et al. Two Caffeoyl-CoA O-methyltransferase-like enzyme are involved in the biosynthesis of polymethoxyflavones in Citrus reticulata ‘Chachiensis’. Int J Biol Macromol. 2025; 310:143277

[63]

WenJ, WangY, LuX. et al. An integrated multi-omics approach reveals polymethoxylated flavonoid biosynthesis in Citrus reticulata cv. Chachiensis. Nat Commun. 2024; 15: 1-18

[64]

Chen Y, Chen Y, Shi C. et al. SOAPnuke: a MapReduce acceleration-supported software for integrated quality control and preprocessing of high-throughput sequencing data. Giga-Science. 2018; 7:1-6

[65]

Xu Q, Chen LL, Ruan X. et al. The draft genome of sweet orange (Citrus sinensis). Nat Genet. 2013; 45:59-66

[66]

Kim D, Paggi JM, Park C. et al. Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype. Nat Biotech. 2019; 37:907-15

[67]

Frazee AC, Pertea G, Jaffe AE. et al. Ballgown bridges the gap between transcriptome assembly and expression analysis. Nat Biotechnol. 2015; 33:243-6

[68]

Love MI, Huber W, Simon A. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014; 15:1-21

[69]

Langfelder P, Horvath S. WGCNA: an R package for weighted correlation network analysis. BMC Bioinformatics. 2008; 9: 1-13

[70]

Bastian M, Heymann S, Jacomy M. Gephi: an open source soft-ware for exploring and manipulating networks. Proc Int AAAI Conf Web Soc Media. 2009; 3:361-2

[71]

Lin R, Ding L, Casola C. et al. Transposase-derived transcription factors regulate light signaling in Arabidopsis. Science. 2007; 318: 1302-5

[72]

Zhao C, Liu X, Gong Q. et al. Three AP2/ERF family members modulate flavonoid synthesis by regulating type IV chalcone isomerase in citrus. Plant Biotechnol J. 2021; 19:671-88

[73]

Wang MM, Zhu QG, Deng CL. et al. Hypoxia-responsive ERFs involved in postdeastringency softening of persimmon fruit. Plant Biotechnol J. 2017; 15:1409-19

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