Studies on the mother flower carnation: past, present, and future

Min Wang , Zhengkang Pi , Zekang Pan , Xilin Li , Linlin Zhong , Yunjiang Cheng , Manzhu Bao , Fan Zhang

Horticulture Research ›› 2025, Vol. 12 ›› Issue (8) : 118

PDF (1317KB)
Horticulture Research ›› 2025, Vol. 12 ›› Issue (8) :118 DOI: 10.1093/hr/uhaf118
Articles
research-article

Studies on the mother flower carnation: past, present, and future

Author information +
History +
PDF (1317KB)

Abstract

Carnation (Dianthus caryophyllus L.) is an important global flower crop, with great ornamental and economic value. It has more than 2000 years of cultivation history and profound cultural heritage known as mother flower. Now, although carnation is deeply loved by the majority of consumers because of its rich color and various varieties, the original carnation unique clove flavor has disappeared. Furthermore, our understanding of carnation traits such as flower shape, flower color, flower fragrance, disease resistance, and vase life remains limited. Previous reviews have primarily concentrated on individual aspects of carnation, failing to present a comprehensive overview. In this review, we summarize the recent progress of carnation in these aspects, so as to provide a reference for the future research direction in carnation.

Cite this article

Download citation ▾
Min Wang, Zhengkang Pi, Zekang Pan, Xilin Li, Linlin Zhong, Yunjiang Cheng, Manzhu Bao, Fan Zhang. Studies on the mother flower carnation: past, present, and future. Horticulture Research, 2025, 12(8): 118 DOI:10.1093/hr/uhaf118

登录浏览全文

4963

注册一个新账户 忘记密码

Acknowledgments

This work was supported by the National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops (Horti-3Y-2024-015), the Knowledge Innovation Program of Wuhan-Basic Research (Program No. 2023020201010106), the Fundamental Research Funds for the Central Universities (Program No. 2662023PY023 and 2662019PY049), the Thousand Youth Talents Plan Project and the Start-up Funding from Huazhong Agricultural University to FZ, and by the Fundamental Research Funds for the Central Universities (Program No. 2662023PY011), the Young Scientist Fostering Funds for the National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops (Program No. Horti-PY-2023-001), and the Yunnan Xingdian Talents-Special Selection Project for High-level Scientific and Technological Talents and Innovation Teams-Team Specific Project (Program No. 202505AS350021).

Author contributions

F.Z. conceived and supervised the project. M.W. prepared the review and wrote the original draft by help with Z.P. (Zhengkang Pi), Z.P. (Zekang Pan) and X.L.. L.Z., Y.C., and M.B. provided suggestions on the manuscript. F.Z. edited the manuscript.

Conflict of interest statement

The authors declare that they have no conflicts of interest.

References

[1]

Nimura M, Kato J, Horaguchi H. et al. Induction of fertile amphidiploids by artificial chromosome-doubling in interspe-cific hybrid between Dianthus caryophyllus L. and D. Japonicus Thunb. Breed Sci. 2006; 56:303-10

[2]

Holley WD, Baker R. Carnation production, including the his-tory, breeding, culture and marketing of carnations. Carnation Production. 1963.

[3]

Harbaugh DT. et al. A new lineage-based tribal CLASSIFICA-TION of the family CARYOPHYLLACEAE. Int J Plant Sci. 171: 185-98

[4]

Committee, F.o.C.E. Dianthus L. FloraofChina. 1996; 26:408

[5]

Sanger F, Nicklen S, Coulson AR. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci. 1977; 74:5463-7

[6]

Ronaghi M, Uhlén M, Nyrén P. A sequencing method based on real-time pyrophosphate. Science. 1998; 281:363-5

[7]

Wenger AM, Peluso P, Rowell WJ. et al. Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome. Nat Biotechnol. 2019; 37: 1155-62

[8]

Hon T, Mars K, Young G. et al. Highly accurate long-read HiFi sequencing data for five complex genomes. Sci Data. 2020; 7:399

[9]

Koren S, Walenz BP, Berlin K. et al. Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation. Genome Res. 2017; 27:722-36

[10]

Xie Y, Wu G, Tang J. et al. SOAPdenovo-trans: de novo tran-scriptome assembly with short RNA-Seq reads. Bioinformatics. 2014; 30:1660-6

[11]

Cheng H, Concepcion GT, Feng X. et al. Haplotype-resolved de novo assembly using phased assembly graphs with hifiasm. Nat Methods. 2021; 18:170-5

[12]

Nurk S, Walenz BP, Rhie A. et al. HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads. Genome Res. 2020; 30:1291-305

[13]

WANG Y, YU J, TANG H. et al. Research status and prospect of plant complex genomes and pan-genomes. Sci Sin Vitae. 2024; 54:233-46

[14]

Jiang H, Zhang X, Leng L. et al. A chromosome-scale and haplotype-resolved genome assembly of carnation (Dianthus caryophyllus) based on high-fidelity sequencing. Front Plant Sci. 2023; 14:12

[15]

Yagi M, Kosugi S, Hirakawa H. et al. Sequence analysis of the genome of carnation (Dianthus caryophyllus L.). DNA Res. 2014; 21:231-41

[16]

Zhang X, Lin S, Peng D. et al. Integrated multi-omic data and analyses reveal the pathways underlying key ornamen-tal traits in carnation flowers. Plant Biotechnol J. 2022; 20: 1182-96

[17]

Lan L, Leng L, Liu W. et al. The haplotype-resolved telomere-to-telomere carnation (Dianthus caryophyllus) genome reveals the correlation between genome architecture and gene expression. Hortic Res. 2024;11:uhad244

[18]

Ni L, Liu Y, Ma X. et al. Pan-3D genome analysis reveals structural and functional differentiation of soybean genomes. Genome Biol. 2023; 24:12

[19]

Lian Q, Huettel B, Walkemeier B. et al. A pan-genome of 69 Arabidopsis thaliana accessions reveals a conserved genome structure throughout the global species range. Nat Genet. 2024; 56:982-91

[20]

Wang M, Li J, Qi Z. et al. Genomic innovation and regulatory rewiring during evolution of the cotton genus Gossypium. Nat Genet. 2022; 54:1959-71

[21]

Li N, He Q, Wang J. et al. Super-pangenome analyses highlight genomic diversity and structural variation across wild and cultivated tomato species. Nat Genet. 2023; 55:852-60

[22]

Tang D, Jia Y, Zhang J. et al. Genome evolution and diversity of wild and cultivated potatoes. Nature. 2022; 606:535-41

[23]

Huang Y, He J, Xu Y. et al. Pangenome analysis provides insight into the evolution of the orange subfamily and a key gene for citric acid accumulation in citrus fruits. Nat Genet. 2023; 55: 1964-75

[24]

Wang T, Duan S, Xu C. et al. Pan-genome analysis of 13 Malus accessions reveals structural and sequence variations associ-ated with fruit traits. Nat Commun. 2023; 14:7377

[25]

Wu D, Xie L, Sun Y. et al. A syntelog-based pan-genome provides insights into rice domestication and de-domestication. Genome Biol. 2023; 24:179

[26]

Wang B, Hou M, Shi J. et al. De novo genome assembly and analyses of 12 founder inbred lines provide insights into maize heterosis. Nat Genet. 2023; 55:312-23

[27]

Xie L, Gong X, Yang K. et al. Technology-enabled great leap in deciphering plant genomes. Nat Plants. 2024; 10:551-66

[28]

Li M, Wen Z, Meng J. et al. The genomics of ornamental plants: current status and opportunities. Ornam Plant Res. 2022; 2:1-18

[29]

Huala E, Dickerman AW, Garcia-Hernandez M. et al. The Arabidopsis information resource (TAIR): a comprehensive database and web-based information retrieval, analysis, and visualization system for a model plant. Nucleic Acids Res. 2001; 29:102-5

[30]

Li H, Yang X, Zhang Y. et al.Nelumbo genome database, an inte-grative resource for gene expression and variants of Nelumbo nucifera. Sci Data. 2021; 8:38

[31]

Fu X, Li S, Zhang Y. et al. DcWRKY15 positively regulates anthocyanin biosynthesis during petal coloration in Dianthus caryophyllus. Plant Physiol Biochem. 2025; 219:109358

[32]

Nakayama M, Koshioka M, Yoshida H. et al. Cyclic malyl antho-cyanins in Dianthus caryophyllus. Phytochemistry. 2000; 55:937-9

[33]

Sasaki N, Matsuba Y, Abe Y. et al. Recent advances in under-standing the anthocyanin modification steps in carnation flowers. Sci Hortic. 2013; 163:37-45

[34]

Okamura M, Nakayama M, Umemoto N. et al. Crossbreeding of a metallic color carnation and diversification of the peculiar coloration by ion-beam irradiation. Euphytica. 2013; 191:45-56

[35]

Holton TA. Transgenic Plants Exhibiting Altered Flower Color and Methods for Producing Same. Victoria, Australia: International Flower Developments Pty. Ltd.; 2000:

[36]

Fukui Y, Tanaka Y, Kusumi T. et al. A rationale for the shift in colour towards blue in transgenic carnation flowers expressing the flavonoid 3 ’,5 ’-hydroxylase gene. Phytochemistry. 2003; 63: 15-23

[37]

Yoshida H, Itoh Y, Ozeki Y. et al. Variation in chalcononarin-genin 2 ’-O-glucoside content in the petals of carnations (Dianthus caryophyllus) bearing yellow flowers. Sci Hortic. 2004; 99:175-86

[38]

Miyahara T, Sugishita N, Ishida-Dei M. et al. Carnation I locus contains two chalcone isomerase genes involved in orange flower coloration. Breed Sci. 2018; 68:481-7

[39]

Totsuka A, Okamoto E, Miyahara T. et al. Repressed expres-sion of a gene for a basic helix-loop-helix protein causes a white flower phenotype in carnation. Breed Sci. 2018; 68: 139-43

[40]

Momose M, Nakayama M, Itoh Y. et al. An active hAT trans-posable element causing bud mutation of carnation by inser-tion into the flavonoid 3’-hydroxylase gene. Mol Gen Genomics. 2013; 288:175-84

[41]

Iijima L, Kishimoto S, Ohmiya A. et al. Esterified carotenoids are synthesized in petals of carnation (Dianthus caryophyl-lus) and accumulate in differentiated chromoplasts. Sci Rep. 2020; 10:15256

[42]

Nakayama M.Flower Pigments Responsible for Cyanic, Yellow, and Cream-White Coloration in Carnation. In: Onozaki T, Yagi M,eds. The Carnation Genome. Springer: Singapore, 2020,61-79

[43]

Morimoto H, Ando Y, Sugihara H. et al. Information on flower coloration and pigmentation in current carnation cultivars for use in future flower-color breeding. Hort J. 2021; 90:428-49

[44]

Deguchi A, Tatsuzawa F, Ishii K. et al. Localized repression of two bHLH genes is involved in the formation of white margins and white Abaxial surfaces in carnation petals by inducing the absence of anthocyanin synthesis. Hort J. 2022; 91:68-84

[45]

Onozaki T, Mato M, Shibata M. et al. Differences in flower color and pigment composition among white carnation (Dianthus caryophyllus L.) cultivars. Sci Hortic. 1999; 82:103-11

[46]

Mato, Onozaki T, Ozeki Y. et al. Flavonoid biosynthesis in pink-flowered cultivars derived from ’William Sim’ carnation (Dianthus caryophyllus). JHorticSci. 2001; 70:315-9

[47]

Yoshida H, Akimoto H, Yamaguchi M. et al. Alteration of methy-lation profiles in distinct cell lineages of the layers during vegetative propagation in carnations (Dianthus caryophyllus). Euphytica. 2004; 135:247-53

[48]

Clery RA, Owen NE, Chambers SF. et al. An investigation into the scent of carnations. J Essent Oil Res. 1999; 11:355-9

[49]

Zuker A, Tzfira T, Ben-Meir H. et al. Modification of flower color and fragrance by antisense suppression of the flavanone 3-hydroxylase gene. Mol Breed. 2002; 9:41

[50]

Kishimoto K, Shibuya K. Scent emissions and expression of scent emission-related genes: a comparison between cut and intact carnation flowers. Sci Hortic. 2021; 281:109920

[51]

Kishimoto K. Effect of post-harvest management on scent emission of carnation cut flowers. Hort J. 2021; 90:341-8

[52]

Anonis DP. The application of carnation in perfumery. Flavour Fragr J. 1985; 1:9-15

[53]

Lavy M. Linalool and linalool oxide production in transgenic carnation flowers expressing the Clarkia breweri linalool syn-thase gene. Mol Breed. 2002; 9:103-11

[54]

Kishimoto K, Nakayama M, Yagi M. et al. Evaluation of wild dianthus species as genetic resources for fragrant carnation breeding based on their floral scent composition. JHorticSci. 2011; 80:175-81

[55]

Kishimoto K, Yagi M, Onozaki T. et al. Analysis of scents emitted from flowers of interspecific hybrids between carna-tion and fragrant wild dianthus species. JHorticSci. 2013; 82: 145-53

[56]

Saunders ER. Studies in the inheritance of doubleness in flow-ers, II.Meconopsis, Althaea and Dianthus. J Genet. 1917; 6:165-84

[57]

Onozaki T. DNA markers linked to a recessive gene controlling single flower type derived from a wild species, Dianthus capita-tus ssp. andrzejowskianus. Hortic Res. 2006; 5:363-7

[58]

Yagi M, Yamamoto T, Isobe S. et al. Identification of tightly linked SSR markers for flower type in carnation (Dianthus caryophyllus L.). Euphytica. 2014; 198:175-83

[59]

Wang Q, Dan N, Zhang X. et al. Identification, characteriza-tion and functional analysis of C-class genes associated with double flower trait in carnation (Dianthus caryphyllus L.). Plants (Basel). 2020; 9:87

[60]

Santos-Rodriguez J, Coy-Barrera E, Ardila HD. Mycelium disper-sion from Fusarium oxysporum f. sp. dianthi elicits a reduction of wilt severity and influences phenolic profiles of carnation (Dianthus caryophyllus L.) roots. Plants (Basel). 2021; 10:1447

[61]

Mora WHP, Castillejo MA, Novo JJ. et al. Thiamine-induced resistance in carnation against Fusarium oxysporum f. sp dianthi and mode of action studies based on the proteomics analysis of root tissue. Sci Hortic. 2024; 323:112549

[62]

Perez-Mora W, Coy-Barrera E, Melgarejo LM. et al. Metabo-lite profiling-based analysis reveals up-regulated shikimate derivatives in carnation roots associated with the thiamine-induced resistance against Fusarium oxysporum f. sp. dianthi. Physiol Mol Plant Pathol. 2025; 136:102535

[63]

Yagi M, Kimura T, Yamamoto T. et al. QTL analysis for resis-tance to bacterial wilt (Burkholderia caryophylli) in carnation (Dianthus caryophyllus) using an SSR-based genetic linkage map. Mol Breed. 2012; 30:495-509

[64]

Jordan R, Korolev E, Grinstead S. et al. First complete genome sequence of carnation latent virus, the type member of the genus Carlavirus. Arch Virol. 2021; 166:1501-5

[65]

Hosseini H, Mehrvar M, Zakiaghl M. The first whole genome sequence and characterization of carnation cryptic virus 3 based on metagenomic analysis of carnation in Iran. Biologia. 2025; 80:499-509

[66]

Jo Y, Choi H, Cho W. Complete genome sequence of a car-nation mottle virus infecting hop plants. Genome Announc. 2015; 3:e00416-15.

[67]

Breit TM, de Leeuw W, van Olst M. et al. Genome sequences of 10 new carnation mottle virus variants. Microbiol Resourc Announc. 2023; 12:e0018923-3

[68]

Lim TK. Edible Medicinal and Non-medicinal Plants. Dordrecht: Springer Netherlands; 2014:

[69]

WanXL, ZhouQ, WangYY. et al. Identification of heat-responsive genes in carnation (Dianthus caryophyllus L.) by RNA-seq. Front Plant Sci. 2015; 6:519

[70]

SunY, HuD, Xue P. et al. Identification of the DcHsp20 gene family in carnation (Dianthus caryophyllus) and functional char-acterization of DcHsp17.8 in heat tolerance. Planta. 2022; 256:2

[71]

Xue P, Sun Y, Hu D. et al. Genome-wide characterization of DcHsp90 gene family in carnation (Dianthus caryophyllus L.) and functional analysis of DcHsp90-6 in heat tolerance. Protoplasma. 2023; 260:807-19

[72]

Li W, Wan X-L, Yu J-Y. et al. Genome-wide identification, Clas-sification, and expression analysis of the Hsf gene family in carnation (Dianthus caryophyllus). Int J Mol Sci. 2019; 20:5233

[73]

Wan XL, Sun YY, Feng Y. et al. Heat stress transcription factor DcHsfA1d isolated from Dianthus caryophyllus enhances thermo-tolerance and salt tolerance of transgenic Arabidopsis. Biol Plant. 2022; 66:29-38

[74]

Zhao M, Liu Z, Xue P. et al. Genomic characterization of the NAC transcription factors in carnation and function analysis of DcNAC41 involved in thermotolerance. Plant Physiol Biochem. 2025; 219:109390

[75]

Hu D, Zhang X, Xue P. et al. Exogenous melatonin ameliorates heat damages by regulating growth, photosynthetic efficiency and leaf ultrastructure of carnation. Plant Physiol Biochem. 2023; 198:107698

[76]

Elmongy MS, Abd El-Baset MM. Melatonin application induced physiological and molecular changes in carnation (Dianthus caryophyllus L.) under heat stress. Horticulturae. 2024; 10:122

[77]

Crocker W, Knight LL. Effect of illuminating gas and ethylene upon flowering carnations - contributions from the hull botan-ical laboratory 116. Bot Gaz. 1908; 46:259-76

[78]

Bowyer MC, Wills RBH, Badiyan D. et al. Extending the posthar-vest life of carnations with nitric oxide - comparison of fumigation and in vivo delivery. Postharvest Biol Technol. 2003; 30: 281-6

[79]

Onozaki T, Yagi M, Tanase K. Selection of carnation line 806-46b with both ultra-long vase life and ethylene resistance. Hort J. 2015; 84:58-68

[80]

Ma N, Ma C, Liu Y. et al. Petal senescence: a hormone view. JExp Bot. 2018; 69:719-32

[81]

Cook EL, Vanstaden J. The carnation AS a model for hormonal studies IN FLOWER senescence. Plant Physiol Biochem. 1988; 26: 793-807

[82]

Burg SP, Dijkman MJ. Ethylene and auxin participation IN pollen INDUDED fading of VANDA orchid blossoms. Plant Phys-iol. 1967; 42:1648-50

[83]

Fu Z, Wang H, Liu J. et al. Cloning and characterization of a DCEIN2 gene responsive to ethylene and sucrose in cut flower carnation. Plant Cell Tissue Org Cult. 2011; 105:447-55

[84]

Iordachescu M, Verlinden S. Transcriptional regulation of three EIN3-like genes of carnation (Dianthus caryophyllus L. cv. Improved white Sim) during flower development and upon wounding, pollination, and ethylene exposure. JExp Bot. 2005; 56:2011-8

[85]

Jones ML, Woodson WR. Differential expression of three mem-bers of the 1-aminocyclopropane-1-carboxylate synthase gene family in carnation. Plant Physiol. 1999; 119:755-64

[86]

Park KY, Drory A, Woodson WR. Molecular-CLONING of an 1-AMINOCYCLOPROPANE-1-carboxylate synthase from senescing carnation FLOWER petals. Plant Mol Biol. 1992; 18: 377-86

[87]

Savin KW, Baudinette SC, Graham MW. et al. Antisense ACC oxidase RNA delays carnation petal senescence. HortScience. 1995; 30:970-2

[88]

Shibuya K, Nagata M, Tanikawa N. et al. Comparison of mRNA levels of three ethylene receptors in senescing flow-ers of carnation (Dianthus caryophyllus L.). JExp Bot. 2002; 53: 399-406

[89]

ten Have A, Woltering EJ. Ethylene biosynthetic genes are dif-ferentially expressed during carnation (Dianthus caryophyllus L.) flower senescence. Plant Mol Biol. 1997; 34:89-97

[90]

Waki K, Shibuya K, Yoshioka T. et al. Cloning of a cDNA encoding EIN3-like protein (DC-EIL1) and decrease in its mRNA level during senescence in carnation flower tissues. JExp Bot. 2001; 52:377-9

[91]

Woodson WR, Park KY, Drory A. et al. Expression of ethylene biosynthetic-pathway transcripts IN senescing carnation flow-ers. Plant Physiol. 1992; 99:526-32

[92]

Norikoshi R, Niki T, Ichimura K. Differential regulation of two 1-aminocyclopropane-1-carboxylate oxidase (ACO) genes, including the additionally cloned DcACO2, during senescence in carnation flowers. Postharvest Biol Technol. 2022; 183:111752

[93]

Yang SF, Hoffman NE. Ethylene biosynthesis and its regulation IN higher-plants. Annu Rev Plant Physiol Plant Mol Biol. 1984; 35: 155-89

[94]

Hua J, Chang C, Sun Q. et al. Ethylene insensitivity conferred by ARABIDOPSIS ERS gene. Science. 1995; 269:1712-4

[95]

Hua J, Meyerowitz EM. Ethylene responses are negatively reg-ulated by a receptor gene family in Arabidopsis thaliana. Cell. 1998; 94:261-71

[96]

Hua J, Sakai H, Nourizadeh S. et al. EIN4 and ERS2 are members of the putative ethylene receptor gene family in Arabidopsis. Plant Cell. 1998; 10:1321-32

[97]

Li W, Ma M, Feng Y. et al. EIN2-directed translational regulation of ethylene signaling in Arabidopsis. Cell. 2015; 163:670-83

[98]

Chang KN, Zhong S, Weirauch MT. et al. Temporal transcrip-tional response to ethylene gas drives growth hormone cross-regulation in Arabidopsis. elife. 2013; 2:e00675

[99]

Wang M, Wang M, Ni C. et al. Differences in ethylene sensitivity, expression of ethylene biosynthetic genes and vase life among carnation varieties. Ornam Plant Res. 2024; 4:e004

[100]

Xu H, Luo D, Zhang F. DcWRKY 75 promotes ethylene induced petal senescence in carnation (Dianthus caryophyllus L.). Plant J. 2021; 108:1473-92

[101]

Xu H, Wang S, Larkin RM. et al. The transcription factors DcHB30 and DcWRKY75 antagonistically regulate ethylene-induced petal senescence in carnation (Dianthus caryophyllus). JExp Bot. 2022; 73:7326-43

[102]

Wang S, Xu H, Zhang F. DcEIL3-1, DcWRKY75 and DcHB30 transcription factors form an activation-inhibition module to regulate petal senescence in carnation (Dianthus caryophyllus L.). Postharvest Biol Technol. 2024; 210:112743

[103]

Wang Y. et al. The negative regulation of DcERF-1 on senescence of cut carnation. Acta Hortic Sin. 2022; 49:1313-26

[104]

Wang T, Sun Z, Wang S. et al. DcWRKY33 promotes petal senescence in carnation (Dianthus caryophyllus L.) by activating genes involved in the biosynthesis of ethylene and abscisic acid and accumulation of reactive oxygen species. Plant J. 2023; 113: 698-715

[105]

SunZ, WuM, WangS. et al. An insertion of transposon in DcNAP inverted its function in the ethylene pathway to delay petal senescence in carnation (Dianthus caryophyllus L.). Plant Biotechnol J. 2023; 21:2307-21

[106]

Zhu C, Huang Z, Sun Z. et al. The mutual regulation between DcEBF1/2 and DcEIL3-1 is involved in ethylene induced petal senescence in carnation (Dianthus caryophyllus L.). Plant J. 2023; 114:636-50

[107]

Zhang F, Qi B, Wang L. et al. EIN2-dependent regulation of acetylation of histone H3K14 and non-canonical histone H3K23 in ethylene signalling. Nat Commun. 2016; 7:13018

[108]

Zhang F, Wang L, Qi B. et al. EIN2 mediates direct regulation of histone acetylation in the ethylene response. Proc Natl Acad Sci USA. 2017; 114:10274-9

[109]

Wang L, Zhang F, Rode S. et al. Ethylene induces combinatorial effects of histone H3 acetylation in gene expression in Ara-bidopsis. BMC Genomics. 2017; 18:538

[110]

Zhang F, Wang L, Ko EE. et al. Histone deacetylases SRT1 and SRT2 interact with ENAP1 to mediate ethylene-induced transcriptional repression. Plant Cell. 2018; 30:153-66

[111]

Wang L, Zhang F, Qiao H. Chromatin regulation in the response of ethylene: nuclear events in ethylene signaling. Small Methods. 2020; 4:1900288

[112]

Wang L, Zhang Z, Zhang F. et al. EIN2-directed histone acetylation requires EIN3-mediated positive feedback regulation in response to ethylene. Plant Cell. 2021; 33: 322-37

[113]

Feng S, Jiang X, Wang R. et al. Histone H3K4 methyltransferase DcATX1 promotes ethylene induced petal senescence in carna-tion. Plant Physiol. 2023; 192:546-64

[114]

Feng S, Jiang X, Huang Z. et al. DNA methylation remod-eled amino acids biosynthesis regulates flower senescence in carnation (Dianthus caryophyllus). New Phytol. 2024; 241: 1605-20

[115]

Wang M, Ni C, Wang R. et al. Variation in longevity of cut and in planta flowers of potted carnation varieties affected by their relationship with ethylene and water. Ornam Plant Res. 2023; 3: 1-11

[116]

Onozaki T, Tanikawa N, Yagi M. et al. Breeding of carnations (Dianthus caryophyllus L.) for long vase life and rapid decrease in ethylene sensitivity of flowers after anthesis. JHorticSci. 2006; 75:256-63

[117]

Onozaki T, Yagi M, Tanase K. et al. Crossings and selec-tions for six generations based on flower vase life to cre-ate lines with ethylene resistance or ultra-long vase life in carnations (Dianthus caryophyllus L.). JHorticSci. 2011; 80: 486-98

[118]

Baoqiong Z, Moutian F, Yunhui Q. et al. Study on the parameters of gene gun transformation of carnation variety "Yunhong No. 2" using GUS transient expression. Agric Technol. 2009; 21:14-6

[119]

Adedeji OS, Naing AH, Kang H. et al. Optimization of protocol for efficient protoplast isolation and transient gene expression in carnation. Sci Hortic. 2022; 299:111057

[120]

Lu J, Bao X, Zhang M. et al. Effect of growth regulators on rooting of carnation (Dianthus caryophyllus) tissue culture seedlings. Int JHortic. 2021; 11:1-6

[121]

Adedeji OS, Naing AH, Campol JR. et al. Influences of fac-tors affecting the induction of high protoplast yield and cal-lus induction in two different carnations. Plant Biotechnol Rep. 2024; 18:375-83

[122]

Lowe K, Wu E, Wang N. et al. Morphogenic regulators baby boom and Wuschel improve monocot transformation. Plant Cell. 2016; 28:1998-2015

[123]

Debernardi JM, Tricoli DM, Ercoli MF. et al. A GRF-GIF chimeric protein improves the regeneration efficiency of transgenic plants. Nat Biotechnol. 2020; 38:1274-9

[124]

Wang K, Shi L, Liang X. et al. The gene TaWOX5 overcomes genotype dependency in wheat genetic transformation. Nat Plants. 2022; 8:110-7

[125]

Du C, Chai LA, Liu C. et al. Improved agrobacterium tumefaciens-mediated transformation using antibiotics and acetosyringone selection in cucumber. Plant Biotechnol Rep. 2022; 16:17-27

[126]

Sivanandhan G, Moon J, Sung C. et al. L-cysteine increases the transformation efficiency of Chinese cabbage (Brassica rapa ssp. pekinensis). Front Plant Sci. 2021; 12:767140

[127]

Manghwar H, Li B, Ding X. et al. CRISPR/Cas Systems in Genome Editing: methodologies and tools for sgRNA design, off-target evaluation, and strategies to mitigate off-target effects. Adv Sci. 2020; 7:1902312

[128]

Zhang Y, Wu Y, Liu Y. et al. Recent progress in medicinal plant transformation and genome editing. Plant Sci J. 2024; 42:242-53

[129]

Miao C, Xiao L, Hua K. et al. Mutations in a subfamily of abscisic acid receptor genes promote rice growth and productivity. Proc Natl Acad Sci USA. 2018; 115:6058-63

[130]

Porto EM, Komor AC, Slaymaker IM. et al. Base editing: advances and therapeutic opportunities. Nat Rev Drug Discov. 2020; 19: 839-59

[131]

Čermák T, Baltes NJ, Čegan R. et al. High-frequency, precise modification of the tomato genome. Genome Biol. 2015; 16:232

[132]

Yu Z, Chen Q, Chen W. et al. Multigene editing via CRISPR/Cas9 guided by a single-sgRNA seed in Arabidopsis. J Integr Plant Biol. 2018; 60:376-81

[133]

Adedeji OS, Naing AH, Kang H. et al. Editing of the ethylene biosynthesis gene in carnation using CRISPR-Cas9 ribonucle-oprotein complex. Plant Methods. 2024; 20:20

[134]

Mori K, Tanase K, Sasaki K. Novel electroporation-based genome editing of carnation plant tissues using RNPs targeting the anthocyanidin synthase gene. Planta. 2024; 259:84

[135]

Li Z, Yagi M, Koyama R. et al. Establishment of regeneration, transformation, and genome editing procedures for a seed-propagated carnation (Dianthus caryophyllus L.) variety. Plant Cell Tissue Org Cult. 2025; 160:8

[136]

Fu X, Tang K. Efficient genome editing in carnation (Dianthus caryophyllus) using the CRISPR/Cas9 system. Acta Hortic. 2023;193-200:193-200

[137]

Mei G, Chen A, Wang Y. et al. A simple and efficient in planta transformation method based on the active regeneration capacity of plants. Plant Commun. 2024; 5: 100822

[138]

Lu J, Li S, Deng S. et al. A method of genetic transformation and gene editing of succulents without tissue culture. Plant Biotechnol J. 2024; 22:1981-8

[139]

Cody JP, Maher MF, Nasti RA. et al. Direct delivery and fast-treated agrobacterium co-culture (fast-TrACC) plant trans-formation methods for Nicotiana benthamiana. Nat Protoc. 2023; 18:81-1070

AI Summary AI Mindmap
PDF (1317KB)

28

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/