The ClWRKY53-ClBCM/ClSGR module controls plant senescence via chlorophyll degradation in watermelon

Shixiang Duan , Yaxin Chen , Yaomiao Guo , Minjuan Zhang , Yueling Wang , Qishuai Kang , Yachen Liu , Sen Yang , Junling Dou , Dongming Liu , Huanhuan Niu , Wenkai Yan , Huayu Zhu , Luming Yang

Horticulture Research ›› 2025, Vol. 12 ›› Issue (12) : 234

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Horticulture Research ›› 2025, Vol. 12 ›› Issue (12) :234 DOI: 10.1093/hr/uhaf234
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The ClWRKY53-ClBCM/ClSGR module controls plant senescence via chlorophyll degradation in watermelon
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Abstract

Senescence is a complex biological process coordinately regulated by multiple genes at the molecular level. Deciphering its regulatory mechanisms holds significant potential for enhancing crop yield and stress resistance. However, the study on identification of senescence-related genes in watermelon has been limited by low genetic diversity. In this study, we identified an early-senescence watermelon inbred line, WM103, which displayed a pale green phenotype at the seedling stage that transitions to yellow at maturity. Genetic analysis indicated the early-senescence phenotype was controlled by a single recessive gene. Combined by BSA-seq and linkage analysis in a large F2 population, we identified Cla97C10G186360 as the candidate gene, which encoded a BALANCE OF CHLOROPHYLL METABOLISM (ClBCM) protein. Further functional validation through virus-induced gene silencing and CRISPR/Cas9-mediated knockout confirmed that the down-regulation and loss of function of ClBCM can accelerate senescence. RNA-seq analysis revealed that the ClBCM was involved in the chlorophyll metabolism pathway, and these chlorophyll degradation-related genes were significantly up-regulated in WM103. Molecular interaction assays revealed a direct physical interaction between ClBCM and ClSGR. Furthermore, we found WRKY family transcription factors were significantly enriched in differentially expressed genes. In vivo and in vitro experiments showed ClWRKY53 directly bound to the ClBCM promoter and suppressed its transcription, thereby promoting chlorophyll degradation and senescence. These findings provide novel insights into the molecular regulation of senescence in watermelon and establish a theoretical framework for genetic improvement of fruit yield and stress tolerance in cucurbit crops.

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Shixiang Duan, Yaxin Chen, Yaomiao Guo, Minjuan Zhang, Yueling Wang, Qishuai Kang, Yachen Liu, Sen Yang, Junling Dou, Dongming Liu, Huanhuan Niu, Wenkai Yan, Huayu Zhu, Luming Yang. The ClWRKY53-ClBCM/ClSGR module controls plant senescence via chlorophyll degradation in watermelon. Horticulture Research, 2025, 12(12): 234 DOI:10.1093/hr/uhaf234

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Acknowledgements

The authors are grateful to members of Yang’s lab for technical assistance and discussions. This research was supported by the National Natural Science Foundation of China (Grant No. 32172602, 32472739), Excellent Youth Foundation of Henan Scientific Committee (Grant No. 242300421030), and Science and Technology Project of the Tibetan Plateau Seed Breeding Technology Innovation Center (No. LSQSCNYQ2025006).

Author contributions

L.Y. and H.Z. designed the research; S.D. and Y.C. conducted the research; Y.G., M.Z., Y.W., Q.K., and Y.L. contributed to the experimental design and data interpretation; S.Y., J.D., D.L., H.N., and W.Y. edited the manuscript; and L.Y., H.Z., and S.D. participated in data analysis and manuscript writing.

Data availability

The raw sequencing data were downloaded from the NCBI Sequence Read Archive (SRA) database (https://www.ncbi.nlm.nih.gov/sra) under accession number PRJNA1293814.

Conflict of interest statement

The authors declare that they have no conflicts of interest.

Supplementary data

Supplementary data is available at Horticulture Research online.

References

[1]

Guo YF, Ren GD, Zhang KW. et al. Leaf senescence: progression, regulation, and application. Mol Hortic. 2021; 1:5

[2]

Avila Ospina L, Moison M, Yoshimoto K. et al. Autophagy, plant senescence, and nutrient recycling. JExp Bot. 2014; 65:3799-811

[3]

Carillo P, Ferrante A. Decoding the intricate metabolic and bio-chemical changes in plant senescence: a focus on chloroplasts and mitochondria. Ann Bot. 2025;30:mcaf003

[4]

Kim HJ, Nam HG, Lim PO. Regulatory network of NAC transcrip-tion factors in leaf senescence. Curr Opin Plant Biol. 2016; 33:48-56

[5]

Rapp YG, Ransbotyn V, Grafi G. Senescence meets dedifferenti-ation. Plants (Basel, Switzerland). 2015; 4:356-68

[6]

WooHR, KimHJ, LimPO. et al. Leaf senescence: systems and dynamics aspects. Annu Rev Plant Biol. 2019; 70:347-76

[7]

Sakuraba Y, Jeong J, Kang MY. et al. Phytochrome-interacting transcription factors PIF4 and PIF5 induce leaf senescence in Arabidopsis. Nat Commun. 2014; 5:4636

[8]

Sakuraba Y, Schelbert S, Park SY. et al. STAY-GREEN and chloro-phyll catabolic enzymes interact at light-harvesting complex II for chlorophyll detoxification during leaf senescence in Ara-bidopsis. Plant Cell. 2012; 24:507-18

[9]

Wu XY, Kuai BK, Jia JZ. et al. Regulation of leaf senescence and crop genetic improvement. J Integr Plant Biol. 2012; 54:936-52

[10]

Li S, Li SC, Tan SY. et al. Transcription factors-regulated leaf senescence in major crops: insights, applications, and chal-lenges. Curr Plant Biol. 2024; 40:100428

[11]

Zhang W, Tang SF, Li XY. et al. Arabidopsis WRKY1 promotes monocarpic senescence by integrative regulation of flowering, leaf senescence, and nitrogen remobilization. Mol Plant. 2024; 17: 1289-306

[12]

Chen QQ, Yan JL, Tong TT. et al. ANAC087 transcription fac-tor positively regulates age-dependent leaf senescence through modulating the expression of multiple target genes in Arabidop-sis. J Integr Plant Biol. 2023; 65:967-84

[13]

Zhao YN, Liu HR, Cao J. et al. FORKHEAD BOX1 promotes leaf senescence via the histone acetyltransferase HAC1 and the tran-scription factors TGA7 and ABF2/3. Plant Cell. 2025;37:koaf170

[14]

Hu DG, Sun CH, Zhang QY. et al. The basic helix-loop-helix transcription factor MdbHLH3 modulates leaf senescence in apple via the regulation of dehydratase-enolase-phosphatase complex 1. Hortic Res. 2020; 7:50

[15]

Wu XW, Xia MX, Su P. et al. MYB transcription factors in plants: a comprehensive review of their discovery, structure, classifica-tion, functional diversity and regulatory mechanism. Int J Biol Macromol. 2024; 282:136652

[16]

Ahmad Z, Ramakrishnan M, Wang CY. et al. Unravelling the role of WRKY transcription factors in leaf senescence: genetic and molecular insights. J Adv Res. 2024; 74:191-206

[17]

Potschin M, Schlienger S, Bieker S. et al. Senescence networking: WRKY18 is an upstream regulator, a downstream target gene, and a protein interaction partner of WRKY53. J Plant Growth Regul. 2014; 33:106-18

[18]

Chen LG, Xiang SY, Chen YL. et al. Arabidopsis WRKY45 interacts with the DELLA protein RGL1 to positively regulate age-triggered leaf senescence. Mol Plant. 2017; 10:1174-89

[19]

Besseau S, Li J, Palva ET. WRKY54 and WRKY70 co-operate as negative regulators of leaf senescence in Arabidopsis thaliana. JExp Bot. 2012; 63:2667-79

[20]

Wang YQ, Cui X, Yang B. et al. WRKY55 transcription factor positively regulates leaf senescence and the defense response by modulating the transcription of genes implicated in the biosynthesis of reactive oxygen species and salicylic acid in Arabidopsis. Development. 2020;147:dev189647

[21]

Zhang YQ, Liu ZJ, Wang XY. et al. DELLA proteins negatively regulate dark-induced senescence and chlorophyll degradation in Arabidopsis through interaction with the transcription factor WRKY6. Plant Cell Rep. 2018; 37:981-92

[22]

Yu YC, Qi YN, Xu JP. et al. Arabidopsis WRKY71 regulates ethylene-mediated leaf senescence by directly activating EIN2, ORE1 and ACS2 genes. Plant J. 2021; 107:1819-36

[23]

Luan YT, Chen ZJ, Fang ZW. et al. PoWRKY71 is involved in Paeonia ostii resistance to drought stress by directly regulating light-harvesting chlorophyll a/b-binding 151 gene. Hortic Res. 2023;10:uhad194

[24]

Chen D, Shi YR, Zhang P. et al. Deletion of the sugar importer gene OsSWEET1b accelerates sugar starvation-promoted leaf senescence in rice. Plant Physiol. 2024; 195:2176-94

[25]

Chen W, Zheng YC, Wang JY. et al. Ethylene-responsive SbWRKY50 suppresses leaf senescence by inhibition of chloro-phyll degradation in sorghum. New Phytol. 2023; 238:1129-45

[26]

Zhou KN, Ren YL, Lv J. et al. Young leaf chlorosis 1, a chloroplast-localized gene required for chlorophyll and lutein accumula-tion during early leaf development in rice. Planta. 2013; 237: 279-92

[27]

Shimoda Y, Ito H, Tanaka A. Conversion of chlorophyll b to chlorophyll a precedes magnesium dechelation for protection against necrosis in Arabidopsis. Plant J. 2012; 72:501-11

[28]

Süssenbacher I, Kreutz CR, Christ B. et al. Hydroxymethylated dioxobilins in senescent Arabidopsis thaliana leaves: sign of a puzzling biosynthetic intermezzo of chlorophyll breakdown. Chemistry. 2015; 21:11664-70

[29]

Liu WK, Chen GL, He MM. et al. ABI5 promotes heat stress-induced chlorophyll degradation by modulating the stability of MYB44 in cucumber. Hortic Res. 2023;10:uhad089

[30]

Ren G, An K, Liao Y. et al. Identification of a novel chloroplast protein AtNYE1 regulating chlorophyll degradation during leaf senescence in Arabidopsis. Plant Physiol. 2007; 144:1429-41

[31]

Chen C, Wang M, Zhu JZ. et al. Long-term effect of epige-netic modification in plant-microbe interactions: modification of DNA methylation induced by plant growth-promoting bacte-ria mediates promotion process. Microbiome. 2022; 10:36

[32]

Schelbert S, Aubry S, Burla B. et al. Pheophytin pheophorbide hydrolase (pheophytinase) is involved in chlorophyll break-down during leaf senescence in Arabidopsis. Plant Cell. 2009; 21: 767-85

[33]

Yu GH, Xie ZN, Lei SS. et al. The NAC factor LpNAL delays leaf senescence by repressing two chlorophyll catabolic genes in perennial ryegrass. Plant Physiol. 2022; 189:595-610

[34]

Pruzinská A, Tanner G, Aubry S. et al. Chlorophyll breakdown in senescent Arabidopsis leaves. Characterization of chlorophyll catabolites and of chlorophyll catabolic enzymes involved in the degreening reaction. Plant Physiol. 2005; 139:52-63

[35]

Jiang HW, Chen YP, Li MR. et al. Overexpression of SGR results in oxidative stress and lesion-mimic cell death in rice seedlings. J Integr Plant Biol. 2011; 53:375-87

[36]

Dou JL, Zhao SJ, Lu XQ. et al. Genetic mapping reveals a candidate gene (ClFS1) for fruit shape in watermelon (Citrullus lanatus L.). Theor Appl Genet. 2018; 131:947-58

[37]

Li BB, Zhao SJ, Dou JL. et al. Genetic mapping and development of molecular markers for a candidate gene locus controlling rind color in watermelon. Theor Appl Genet. 2019; 132:2741-53

[38]

Wang DK, Zhang M, Xu NN. et al. Fine mapping a ClGS gene controlling dark-green stripe rind in watermelon. Sci Hortic. 2022; 291:110583

[39]

Liu DM, Yang HH, Yuan YX. et al. Comparative transcriptome analysis provides insights into yellow rind formation and pre-liminary mapping of the Clyr (yellow rind) gene in watermelon. Front Plant Sci. 2020; 11:192

[40]

Liu D, Liang J, Liu Q. et al. The pseudo-type response regulator gene Clsc regulates rind stripe coloration in watermelon. J Integr Agric. 2025; 24:147-60

[41]

Zhu HY, Zhang MJ, Sun SR. et al. A single nucleotide deletion in an ABC transporter gene leads to a dwarf phenotype in watermelon. Front Plant Sci. 2019; 10:1399

[42]

Dou JL, Yang HH, Sun D. et al. The branchless gene Clbl in watermelon encoding a TERMINAL FLOWER 1 protein regulates the number of lateral branches. Theor Appl Genet. 2022; 135: 65-79

[43]

Duan SX, Guo YM, Wang YP. et al. HD-zip transcription factor is responsible for no-lobed leaf in watermelon (Citrullus lanatus L.). Phyton-Int J Exp Bot. 2023; 92:1311-28

[44]

Wei CH, Zhang RM, Yue Z. et al. The impaired biosynthetic net-works in defective tapetum lead to male sterility in watermelon. JProteomics. 2021; 243:104241

[45]

Liu D, Zhang L, Hu A. et al. The MYB transcription factor ClPC modulates petal color and chlorophyll accumulation in water-melon. Plant Sci. 2025; 359:112586

[46]

Deng Y, Liu X, Liu SC. et al. Fine mapping of ClLOX, a QTL for powdery mildew resistance in watermelon (Citrullus lanatus L.). Theor Appl Genet. 2024; 137:51

[47]

Guo SG, Zhao SJ, Sun HH. et al. Resequencing of 414 cultivated and wild watermelon accessions identifies selection for fruit quality traits. Nat Genet. 2019; 51:1616-23

[48]

Barham WS. A study of the Royal Golden watermelon with emphasis on the inheritance of the chlorotic condition charac-teristic of this variety. Proc Am Soc Hortic Sci. 1956; 67:487-9

[49]

Wang P, Richter AS, Kleeberg JRW. et al. Post-translational coor-dination of chlorophyll biosynthesis and breakdown by BCMs maintains chlorophyll homeostasis during leaf development. Nat Commun. 2020; 11:1254

[50]

Liu MF, Wang YQ, Nie ZX. et al. Double mutation of two homolo-gous genes YL1 and YL2 results in a leaf yellowing phenotype in soybean [Glycine max (L.) Merr]. Plant Mol Biol. 2020; 103:527-43

[51]

Liu GZ, Yu HY, Yuan L. et al. SlRCM1, which encodes tomato Lutescent1, is required for chlorophyll synthesis and chloroplast development in fruits. Hortic Res. 2021; 8:128

[52]

Yamatani H, Ito T, Nishimura K. et al. Genetic analysis of chlorophyll synthesis and degradation regulated by BAL-ANCE of CHLOROPHYLL METABOLISM. Plant Physiol. 2022; 189: 419-32

[53]

Fu DL, Zhou HL, Grimm B. et al. The BCM1-EGY1 module bal-ances chlorophyll biosynthesis and breakdown to confer chloro-phyll homeostasis in land plants. Mol Plant. 2025; 18:76-94

[54]

Burdiak P, Mielecki J, Gawroński P. et al. The CRK5 and WRKY53 are conditional regulators of senescence and stomatal conduc-tance in Arabidopsis. Cells. 2022; 11:3558

[55]

Wang ZR, Gao M, Li YF. et al. The transcription factor SlWRKY37 positively regulates jasmonic acid-and dark-induced leaf senes-cence in tomato. JExp Bot. 2022; 73:6207-25

[56]

Gao Y, Shi X, Chang YY. et al. Mapping the gene of a maize leaf senescence mutant and understanding the senescence path-ways by expression analysis. Plant Cell Rep. 2023; 42:1651-63

[57]

Yang X, Gong P, Li KY. et al. A single cytosine deletion in the OsPLS1 gene encoding vacuolar-type H+-ATPase subunit A1 leads to premature leaf senescence and seed dormancy in rice. JExpBot. 2016; 67:2761-76

[58]

Zhang WJ, Zhang ZH, Chen Q. et al. Mutation of a highly con-served amino acid in RPM1 causes leaf yellowing and premature senescence in wheat. Theor Appl Genet. 2023; 136:254

[59]

Qiao YL, Jiang WZ, Lee J. et al. SPL28 encodes a clathrin-associated adaptor protein complex 1, medium subunit micro 1 (AP1M1) and is responsible for spotted leaf and early senescence in rice (Oryza sativa). New Phytol. 2010; 185:258-74

[60]

Qiu L, Fang RM, Jia Y. et al. The allelic mutation of NBS-LRR gene causes premature senescence in wheat. Plant Sci. 2025; 352: 112395

[61]

Zhang LL, Zhang R, Ye X. et al. Overexpressing VvWRKY18 from grapevine reduces the drought tolerance in Arabidopsis by increasing leaf stomatal density. J Plant Physiol. 2022; 275: 153741

[62]

Guo Y, Cai Z, Gan S. Transcriptome of Arabidopsis leaf senes-cence. Plant Cell Environ. 2010; 27:521-49

[63]

Zentgraf U, Doll J. Arabidopsis WRKY53, a node of multi-layer regulation in the network of senescence. Plants. 2019; 8:578

[64]

Wang Q, Li XL, Guo C. et al. Senescence-related receptor kinase 1 functions downstream of WRKY53 in regulating leaf senescence in Arabidopsis. JExp Bot. 2023; 74:5140-52

[65]

Lichtenthaler HK. Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. Methods Enzymol. 1987; 148: 350-82

[66]

Duan SX, Wang DK, Kang QS. et al. The development of liquid-phase chip by target sequencing and their application in water-melon molecular breeding. Hortic Plant J. https://doi.org/10.1016/j.hpj.2025.01.009

[67]

Zhu H, Song P, Koo DH. et al. Genome wide characterization of simple sequence repeats in watermelon genome and their appli-cation in comparative mapping and genetic diversity analysis. BMC Genomics. 2016; 17:557

[68]

Liu M, Liang ZL, Aranda MA. et al. A cucumber green mottle mosaic virus vector for virus-induced gene silencing in cucurbit plants. Plant Methods. 2020; 16:9

[69]

Jiang YX, Zhang AR, He WJ. et al. GRAS family member LATERAL SUPPRESSOR regulates the initiation and morpho-genesis of watermelon lateral organs. Plant Physiol. 2023; 193: 2592-604

[70]

Zhao LJ, Fan PF, Wang YL. et al. ELONGATED HYPOTCOTYL5 and SPINE BASE SIZE1 together mediate light-regulated spine expansion in cucumber. Plant Physiol. 2024; 195:552-65

[71]

Wang XB, Wang QP, Yan LX. et al. PpTCP18 is upregulated by lncRNA5 and controls branch number in peach (Prunus persica) through positive feedback regulation of strigolactone biosynthe-sis. Hortic Res. 2023;10:uhac224

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