Rose Genomics Research Associated with Important Agronomic and Ornamental Traits for Biobreeding: Progress, Challenges and Prospects

Bingjie Zhang , Wenran Wang , Yihan He , Linlin Song , Xiaoming Sun , Changxi Chen , Nan Ma , Cai-Zhong Jiang , Yunhe Jiang , Junping Gao

Biobreeding ›› 2026, Vol. 1 ›› Issue (3) : 10011

PDF (1108KB)
Biobreeding ›› 2026, Vol. 1 ›› Issue (3) :10011 DOI: 10.70322/biobreeding.2026.10011
Review
research-article
Rose Genomics Research Associated with Important Agronomic and Ornamental Traits for Biobreeding: Progress, Challenges and Prospects
Author information +
History +
PDF (1108KB)

Abstract

Rose is a globally significant ornamental crop and an emerging genomics system for woody ornamental plants. In recent decades, the rapid evolution of high-throughput sequencing and robust technical platforms has yielded high-quality reference genomes and been propelling our understanding of rose biology to unprecedented depths. This review systematically synthesizes the current landscape of rose genomics, recent development of technical and resource platforms, and the molecular mechanisms underlying pivotal agronomic traits such as floral development, scent biosynthesis, petal lifespan, and stress resilience. Despite these strides, high genome heterozygosity, polyploidy, and recalcitrance to genetic transformation remain significant barriers. We discuss how integrating cutting-edge technologies, such as pangenomics, single-cell transcriptomics, AI-assisted genomic selection, and precise CRISPR-based editing, can bridge the gap between fundamental research and practical applications. Collectively, this review provides a strategic roadmap for accelerating the development of next-generation rose cultivars through trait-based biobreeding.

Keywords

Rose (Rosa) / Functional genomics / Technical and resource platforms / Agronomic trait genes / Gene editing

Cite this article

Download citation ▾
Bingjie Zhang, Wenran Wang, Yihan He, Linlin Song, Xiaoming Sun, Changxi Chen, Nan Ma, Cai-Zhong Jiang, Yunhe Jiang, Junping Gao. Rose Genomics Research Associated with Important Agronomic and Ornamental Traits for Biobreeding: Progress, Challenges and Prospects. Biobreeding, 2026, 1 (3) : 10011 DOI:10.70322/biobreeding.2026.10011

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Hibrand Saint-Oyant L, Ruttink T, Hamama L, Kirov I, Lakhwani D, Zhou NN, et al. A high-quality genome sequence of Rosa chinensis to elucidate ornamental traits. Nat. Plants 2018, 4, 473-484. DOI: 10.1038/s41477-018-0166-1

[2]

de Vries DP, Dubois LAM. Rose breeding: Past, present, prospects. Acta Hortic. 1996, 424, 241-248. DOI: 10.17660/ActaHortic.1996.424.43

[3]

Bendahmane M, Dubois A, Raymond O, Bris ML. Genetics and genomics of flower initiation and development in roses. J. Exp. Bot. 2013, 64, 847-857. DOI: 10.1093/jxb/ers387

[4]

Roberts AV. Encyclopedia of Rose Science; Academic Press: Cambridge, MA, USA, 2003.

[5]

Esselink G, Smulders M, Vosman B. Identification of cut rose (Rosa hybrida) and rootstock varieties using robust sequence tagged microsatellite site markers. Theor. Appl. Genet. 2003, 106, 277-286. DOI: 10.1007/s00122-002-1122-y

[6]

Fougère-Danezan M, Joly S, Bruneau A, Gao XF, Zhang LB. Phylogeny and biogeography of wild roses with specific attention to polyploids. Ann. Bot. 2015, 115, 275-291. DOI: 10.1093/aob/mcu245

[7]

Zhang Z, Yang T, Liu Y, Wu S, Sun H, Wu J, et al. Haplotype-resolved genome assembly and resequencing provide insights into the origin and breeding of modern rose. Nat. Plants 2024, 10, 1659-1671. DOI: 10.1038/s41477-024-01820-x

[8]

Zhou L, Wu S, Chen Y, Huang R, Cheng B, Mao Q, et al. Multi-omics analyzes of Rosa gigantea illuminate tea scent biosynthesis and release mechanisms. Nat. Commun. 2024, 15, 8469. DOI: 10.1038/s41467-024-52782-9

[9]

Cheng B, Zhao K, Zhou M, Bourke PM, Zhou L, Wu S, et al. Phenotypic and genomic signatures across wild Rosa species open new horizons for modern rose breeding. Nat. Plants 2025, 11, 775-789. DOI: 10.1038/s41477-025-01955-5

[10]

Liu D, Liu K, Tong B, Guo H, Qu K, Xu T, et al. Telomere-to-telomere, gap-free assembly of the Rosa rugosa reference genome. Hortic. Plant J. 2024, 12, 1450-1464. DOI: 10.1016/j.hpj.2024.06.005

[11]

Kim CK, Chung JD, Park SH, Burrell AM, Kamo KK, Byrne DH. Agrobacterium tumefaciens-mediated transformation of Rosa hybrida using the green fluorescent protein (gfp) gene. Plant Cell Tissue Organ Cult. 2004, 78, 107-111. DOI: 10.1023/B:TICU.0000022529.16697.90

[12]

Liu G, Yuan Y, Jiang H, Bao Y, Ning G, Zhao L, et al. Agrobacterium tumefaciens-mediated transformation of modern rose (Rosa hybrida) using leaf-derived embryogenic callus. Hortic. Plant J. 2021, 7, 359-366. DOI: 10.1016/j.hpj.2021.02.001

[13]

Wang C, Li Y, Wang N, Yu Q, Li Y, Gao J, et al. An efficient CRISPR/Cas9 platform for targeted genome editing in rose (Rosa hybrida). J. Integr. Plant Biol. 2023, 65, 895-899. DOI: 10.1111/jipb.13421

[14]

Bourke PM, Arens P, Voorrips RE, Esselink GD, Koning-Boucoiran CFS, van't Westende WPC, et al. Partial preferential chromosome pairing is genotype dependent in tetraploid rose. Plant J. 2017, 90, 330-343. DOI: 10.1111/tpj.13496

[15]

Raymond O, Gouzy J, Just J, Badouin H, Verdenaud M, Lemainque A, et al. The Rosa genome provides new insights into the domestication of modern roses. Nat. Genet. 2018, 50, 772-777. DOI: 10.1038/s41588-018-0110-3

[16]

Zhang X, Wu Q, Lan L, Peng D, Guan H, Luo K, et al. Haplotype-resolved genome assembly of the diploid Rosa chinensis provides insight into the mechanisms underlying key ornamental traits. Mol. Hortic. 2024, 4, 14. DOI: 10.1186/s43897-024-00088-1

[17]

Zhang X, Lan L, Yang Y, Guan H, Peng D, Jiang H, et al. Pangenomic analyses of rose uncover widespread structure variation and empower genomics-directed breeding. Nat. Genet. 2026, 58, 1164-1175. DOI: 10.1038/s41588-026-02569-z

[18]

Gahlaut V, Kumari P, Jaiswal V, Kumar S. Genetics, genomics and breeding in Rosa species. J. Hortic. Sci. Biotechnol. 2021, 96, 545-559. DOI: 10.1080/14620316.2021.1894078

[19]

Firoozabady E, Moy Y, Courtney-Gutterson N, Robinson K. Regeneration of transgenic rose (Rosa hybrida) plants from embryogenic tissue. Nat. Biotechnol. 1994, 12, 609-613. DOI: 10.1038/nbt0694-609

[20]

Marchant R, Power JB, Lucas JA, Davey MR. Biolistic transformation of rose (Rosa hybrida L.). Ann. Bot. 1998, 81, 109-114. DOI: 10.1006/anbo.1997.0538

[21]

Wang P, Si H, Li C, Xu Z, Guo H, Jin S, et al. Plant genetic transformation: Achievements, current status and future prospects. Plant Biotechnol. J. 2025, 23, 2034-2058. DOI: 10.1111/pbi.70028

[22]

Kaur N, Pati PK, Sharma M, Ahuja PS. Somatic embryogenesis from immature zygotic embryos of Rosa bourboniana desp. In Vitro Cell. Dev. Biol.-Plant 2006, 42, 124-127. DOI: 10.1079/IVP2005737

[23]

Lu J, Huang Y, Guo Y, Fan C, Yuan G, Zhou R, et al. Agrobacterium rhizogenes-Mediated Hairy Root Transformation in Rosa. Horticulturae 2025, 11, 49. DOI: 10.3390/horticulturae11010049

[24]

Zhang T, Liu K, Chen J, Zhao S, Zhou W, Chen S, et al. An efficient hairy root transformation system for protein interaction and gene editing analysis in roses. Hortic. Plant J. 2025, in press. DOI: 10.1016/j.hpj.2025.03.013

[25]

Nelson A, Ranney T, Liu W, Kelliher T, Duan H, Da K. Overcoming recalcitrance: A review of regeneration methods and challenges in roses. Plants 2025, 14, 3797. DOI: 10.3390/plants14243797

[26]

Rout GR, Debata BK, Das P. Somatic embryogenesis in callus cultures of Rosa hybrida L. cv. Landora. Plant Cell Tissue Organ Cult. 1991, 27, 65-69. DOI: 10.1007/BF00048208

[27]

Yokoya K, Walker S, Sarasan V. Regeneration of rose plants from cell and tissue cultures. Acta Hortic. 1996, 424, 333-338. DOI: 10.17660/ActaHortic.1996.424.61

[28]

Doench JG, Fusi N, Sullender M, Hegde M, Vaimberg EW, Donovan KF, et al. Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9. Nat. Biotechnol. 2016, 34, 184-191. DOI: 10.1038/nbt.3437

[29]

Mao Y, Botella JR, Liu Y, Zhu JK. Gene editing in plants: Progress and challenges. Natl. Sci. Rev. 2019, 6, 421-437. DOI: 10.1093/nsr/nwz005

[30]

Gao C. Genome engineering for crop improvement and future agriculture. Cell 2021, 184, 1621-1635. DOI: 10.1016/j.cell.2021.01.005

[31]

Zhao Y, Liang Y, Ni Z, Sun Q, Zong Y, Wang Y. Advances and prospects of large DNA fragment editing in plants. Nat. Plants 2025, 11, 2461-2475. DOI: 10.1038/s41477-025-02160-0

[32]

Su N, Wang M, Zhang R, Xiao Y, Zhang D, Song Y. Precision editing without footprints: Advancing transgene-free systems in plants. Curr. Plant Biol. 2026, 46, 100588. DOI: 10.1016/j.cpb.2026.100588

[33]

Sun J, Lu J, Bai M, Chen Y, Wang W, Fan C, et al. Phytochrome-interacting factors interact with transcription factor CONSTANS to suppress flowering in rose. Plant Physiol. 2021, 186, 1186-1201. DOI: 10.1093/plphys/kiab109

[34]

Yu R, Xiong Z, Zhu X, Feng P, Hu Z, Fang R, et al. RcSPL1-RcTAF15b regulates the flowering time of rose (Rosa chinensis). Hortic. Res. 2023, 10, uhad083. DOI: 10.1093/hr/uhad083

[35]

Iwata H, Gaston A, Remay A, Thouroude T, Jeauffre J, Kawamura K, et al. The TFL1 homologue KSN is a regulator of continuous flowering in rose and strawberry. Plant. J. 2012, 69, 116-125. DOI: 10.1111/j.1365-313X.2011.04776.x

[36]

Randoux M, Jeauffre J, Thouroude T, Vasseur F, Hamama L, Juchaux M, et al. Gibberellins regulate the transcription of the continuous flowering regulator, RoKSN, a rose TFL1 homologue. J. Exp. Bot. 2012, 63, 6543-6554. DOI: 10.1093/jxb/ers310

[37]

Soufflet-Freslon V, Araou E, Jeauffre J, Thouroude T, Chastellier A, Michel G, et al. Diversity and selection of the continuous-flowering gene, RoKSN, in rose. Hortic. Res. 2021, 8, 76. DOI: 10.1038/s41438-021-00512-3

[38]

Hamama L, Bosselut J, Voisine L, Thouroude T, Ogé L, Chameau J, et al. Rose FT homologous gene overexpression affects flowering and vegetative development behavior in two different rose genotypes. Plant Cell Tissue Organ Cult. 2024, 156, 87. DOI: 10.1007/s11240-024-02695-8

[39]

Sun J, Liu H, Wang W, Fan C, Yuan G, Zhou R, et al. RcOST1L phosphorylates RcPIF4 for proteasomal degradation to promote flowering in rose. New Phytol. 2024, 243, 1387-1405. DOI: 10.1111/nph.19885

[40]

Wang W, Sun J, Fan C, Yuan G, Zhou R, Lu J, et al. RcSRR1 interferes with the RcCSN5B-mediated deneddylation of RcCRL4 to modulate RcCO proteolysis and prevent rose flowering under red light. Hortic. Res. 2025, 12, uhaf025. DOI: 10.1093/hr/uhaf025

[41]

Franklin KA, Praekelt U, Stoddart WM, Billingham OE, Halliday KJ, Whitelam GC. Phytochromes B, D, and E act redundantly to control multiple physiological responses in Arabidopsis. Plant Physiol. 2003, 131, 1340-1346. DOI: 10.1104/pp.102.015487

[42]

Galvāo VC, Fiorucci AS, Trevisan M, Franco-Zorilla JM, Goyal A, Schmid-Siegert E, et al. PIF transcription factors link a neighbor threat cue to accelerated reproduction in Arabidopsis. Nat. Commun. 2019, 10, 4005. DOI: 10.1038/s41467-019-11882-7

[43]

Wang LN, Liu YF, Zhang YM, Fang RX, Liu QL. The expression level of Rosa Terminal Flower 1 (RTFL1) is related with recurrent flowering in roses. Mol. Biol. Rep. 2012, 39, 3737-3746. DOI: 10.1007/s11033-011-1149-8

[44]

Randoux M, Davière J, Jeauffre J, Thouroude T, Pierre S, Toualbia Y, et al. RoKSN, a floral repressor, forms protein complexes with RoFD and RoFT to regulate vegetative and reproductive development in rose. New Phytol. 2014, 202, 161-173. DOI: 10.1111/nph.12625

[45]

Bai M, Liu J, Fan C, Chen Y, Chen H, Lu J, et al. KSN heterozygosity is associated with continuous flowering of Rosa rugosa purple branch. Hortic. Res. 2021, 8, 26. DOI: 10.1038/s41438-021-00464-8

[46]

Peng Y, Li Q, Gong Y, Yang Q, Dong Q, Han Y. RcPLATZ8 as a novel negative regulator of flowering in Rosa chinensis. Plant Cell Rep. 2025, 44, 125. DOI: 10.1007/s00299-025-03513-x

[47]

Jing W, Gong F, Liu G, Deng Y, Liu J, Yang W, et al. Petal size is controlled by the MYB73/TPL/HDA19-miR159-CKX6 module regulating cytokinin catabolism in Rosa hybrida. Nat. Commun. 2023, 14, 7106. DOI: 10.1038/s41467-023-42914-y

[48]

Wang Y, Qin M, Zhang G, Lu J, Zhang C, Ma N, et al. Transcription factor RhRAP2.4L orchestrates cell proliferation and expansion to control petal size in rose. Plant Physiol. 2024, 194, 2338-2353. DOI: 10.1093/plphys/kiad657

[49]

Jin W, Gong F, Zhang Y, Wang R, Liu H, Wei Y, et al. Cytokinin-responsive RhRR1-RhSCL28 transcription factor module positively regulates petal size by promoting cell division in rose. J. Exp. Bot. 2025, 76, 381-392. DOI: 10.1093/jxb/erae331

[50]

Pei H, Ma N, Tian J, Luo J, Chen J, Li J, et al. An NAC transcription factor controls ethylene-regulated cell expansion in flower petals. Plant Physiol. 2013, 163, 775-791. DOI: 10.1104/pp.113.223388

[51]

Luo J, Ma N, Pei H, Chen J, Li J, Gao J. A DELLA gene, RhGAI1, is a direct target of EIN3 and mediates ethylene-regulated rose petal cell expansion via repressing the expression of RhCesA2. J. Exp. Bot. 2013, 64, 5075-5084. DOI: 10.1093/jxb/ert296

[52]

Ma N, Xue J, Li Y, Liu X, Dai F, Jia W, et al. Rh-PIP2;1, a rose aquaporin gene, is involved in ethylene-regulated petal expansion. Plant Physiol. 2008, 148, 894-907. DOI: 10.1104/pp.108.120154

[53]

Wei Y, Zhang Y, Li J, Gong F, Hua W, Liu H, et al. Unravelling the role of phytosulfokine (PSK) in regulating rose petal growth through cell proliferation. Plant J. 2025, 123, e70424. DOI: 10.1111/tpj.70424

[54]

Chen C, Hussain N, Ma Y, Zuo L, Jiang Y, Sun X, et al. The ARF2-MYB6 module mediates auxin-regulated petal expansion in rose. J. Exp. Bot. 2023, 74, 4489-4502. DOI: 10.1093/jxb/erad173

[55]

Gong F, Jing W, Jin W, Liu H, Zhang Y, Wang R, et al. RhMYC2 controls petal size through synergistic regulation of jasmonic acid and cytokinin signaling in rose. Plant J. 2024, 120, 459-472. DOI: 10.1111/tpj.16993

[56]

Gong F, Wang X, Zhao Q, Wang D, Yan H, Wang Q, et al. The GAs-RhMYB70 feedback loop fine-tunes cell expansion and petal size by modulating cellulose content in rose. Hortic. Res. 2025, 12, uhaf134. DOI: 10.1093/hr/uhaf134

[57]

Wang R, Guo Y, Qiu Y, Liu Y, Gong F, Li P, et al. Ethylene restrains brassinosteroid-driven petal growth through RhMPK7-mediated phosphorylation of RhBZR1 in rose. New Phytol. 2026. DOI: 10.1111/nph.71247

[58]

Ji S, Yang Y, Yang S, Jiang S, Cheng H, Liu T, et al. RcAP2L-RcAS1 complex modulates petal number in roses by targeting RcAGL80 promoter. Plant J. 2025, 124, e70549. DOI: 10.1111/tpj.70549

[59]

Chen W, Ding Z, Shen Y, Zhou Y, Luo P, Cui Y. Dioxygenase RhDAO1 regulates floral organ identity by controlling auxin homeostasis in miniature rose (Rosa hybrida). Hortic. Plant J. 2026, 12, 1185-1203. DOI: 10.1016/j.hpj.2025.10.011

[60]

Chen J, Li Y, Li Y, Li Y, Wang Y, Jiang C, et al. AUXIN RESPONSE FACTOR 18-HISTONE DEACETYLASE 6 module regulates floral organ identity in rose (Rosa hybrida). Plant Physiol. 2021, 186, 1074-1087. DOI: 10.1093/plphys/kiab130

[61]

Cheng C, Yu Q, Wang Y, Wang H, Dong Y, Ji Y, et al. Ethylene-regulated asymmetric growth of the petal base promotes flower opening in rose (Rosa hybrida). Plant Cell 2021, 33, 1229-1251. DOI: 10.1093/plcell/koab031

[62]

Ma N, Ma C, Liu Y, Shahid MO, Wang C, Gao J. Petal senescence: A hormone view. J. Exp. Bot. 2018, 69, 719-732. DOI: 10.1093/jxb/ery009

[63]

Ma N, Cai L, Lu W, Tan H, Gao J. Exogenous ethylene influences flower opening of cut roses (Rosa hybrida) by regulating the genes encoding ethylene biosynthesis enzymes. Sci. China Ser. C Life Sci. 2005, 48, 434-444. DOI: 10.1360/062004-37

[64]

Lu J, Zhang G, Ma C, Li Y, Jiang C, Wang Y, et al. The F-box protein RhSAF destabilizes the gibberellic acid receptor RhGID1 to mediate ethylene-induced petal senescence in rose. Plant Cell 2024, 36, 1736-1754. DOI: 10.1093/plcell/koae035

[65]

Ma N, Tan H, Liu X, Xue J, Li Y, Gao J. Transcriptional regulation of ethylene receptor and CTR genes involved in ethylene-induced flower opening in cut rose (Rosa hybrida) cv. Samantha. J. Exp. Bot. 2006, 57, 2763-2773. DOI: 10.1093/jxb/erl033

[66]

Tan H, Liu X, Ma N, Xue J, Lu W, Bai J, et al. Ethylene-influenced flower opening and expression of genes encoding ETRs, CTRs, and EIN3s in two cut rose cultivars. Postharvest Biol. Technol. 2006, 40, 97-105. DOI: 10.1016/j.postharvbio.2006.01.007

[67]

Wu Y, Zuo L, Ma Y, Jiang Y, Gao J, Tao J, et al. Protein kinase rhcipk6 promotes petal senescence in response to ethylene in rose (Rosa Hybrida). Genes 2022, 13, 1989. DOI: 10.3390/genes13111989

[68]

Lü P, Zhang C, Liu J, Liu X, Jiang G, Jiang X, et al. RhHB1 mediates the antagonism of gibberellins to ABA and ethylene during rose (Rosa hybrida) petal senescence. Plant J. 2014, 78, 578-590. DOI: 10.1111/tpj.12494

[69]

Luo J, Chen S, Cao S, Zhang T, Li R, Chan ZL, et al. Rose (Rosa hybrida) ethylene responsive factor 3 promotes rose flower senescence via direct activation of the abscisic acid synthesis-related 9-CIS-EPOXYCAROTENOID DIOXYGENASE Gene. Plant Cell Physiol. 2021, 62, 1030-1043. DOI: 10.1093/pcp/pcab085

[70]

Wu L, Ma N, Jia Y, Zhang Y, Feng M, Jiang CZ, et al. An ethylene-induced regulatory module delays flower senescence by regulating cytokinin content. Plant Physiol. 2017, 173, 853-862. DOI: 10.1104/pp.16.01064

[71]

Khaskheli AJ, Ahmed W, Ma C, Zhang S, Liu Y, Li Y, et al. RhERF113 functions in ethylene-induced petal senescence by modulating cytokinin content in rose. Plant Cell Physiol. 2018, 59, 2442-2451. DOI: 10.1093/pcp/pcy162

[72]

Chen C, Ma Y, Zuo L, Xiao Y, Jiang Y, Gao J. The CALCINEURIN B-LIKE 4/CBL-INTERACTING PROTEIN 3 module degrades repressor JAZ5 during rose petal senescence. Plant Physiol. 2023, 193, 1605-1620. DOI: 10.1093/plphys/kiad365

[73]

Zhang S, Zhao Q, Zeng D, Xu J, Zhou H, Wang F, et al. RhMYB108, an R2R3-MYB transcription factor, is involved in ethylene- and JA-induced petal senescence in rose plants. Hortic. Res. 2019, 6, 131. DOI: 10.1038/s41438-019-0221-8

[74]

Qin M, Wu Z, Zhang C, Jiang Y, Jiang CZ, Sun X, et al. The histone deacetylase RhHDA15 represses petal senescence by epigenetically regulating reactive oxygen species homeostasis in rose. Plant Physiol. 2024, 197, kiae612. DOI: 10.1093/plphys/kiae612

[75]

Jiang L, Liu K, Zhang T, Chen J, Zhao S, Cui Y, et al. The RhWRKY33a-RhPLATZ9 regulatory module delays petal senescence by suppressing rapid reactive oxygen species accumulation in rose flowers. Plant J. 2023, 114, 1425-1442. DOI: 10.1111/tpj.16202

[76]

Zhang Y, Wu Z, Feng M, Chen J, Qin M, Wang W, et al. The circadian-controlled PIF8-BBX28 module regulates petal senescence in rose flowers by governing mitochondrial ROS homeostasis at night. Plant Cell 2021, 33, 2716-2735. DOI: 10.1093/plcell/koab152

[77]

Li P, Qiu Y, Wang R, Zhang B, Ma Y, Sun X, et al. The homeodomain leucine zipper protein RhHB22 promotes petal senescence by repressing ascorbic acid biosynthesis in rose. J. Exp. Bot. 2025, 76, 1704-1717. DOI: 10.1093/jxb/erae503

[78]

Wang W, Chen C, Zhao Y, Zhang B, Wu Z, Sun X, et al. Transcription factors RhPIF4/8 and RhHY5 regulate autophagy-mediated petal senescence in rose (Rosa hybrida). Hortic. Adv. 2023, 1, 17. DOI: 10.1007/s44281-023-00021-4

[79]

Gao Y, Liu Y, Liang Y, Lu J, Jiang C, Fei Z, et al. Rosa hybrida RhERF1 and RhERF4 mediate ethylene- and auxin-regulated petal abscission by influencing pectin degradation. Plant. J. 2019, 99, 1159-1171. DOI: 10.1111/tpj.14412

[80]

Zhao Q, Zhou X, Chen Q, Yang R, Li Y, Zhao J, et al. ER-related E2-E3 ubiquitin enzyme pair regulates ethylene response by modulating the turnover of ethylene receptors. Nat. Commun. 2025, 16, 5937. DOI: 10.1038/s41467-025-61066-9

[81]

Zhang B, Xiao Y, Liu Y, Wang W, Li P, Wang R, et al. The RhMPK3-RhLOB41-RhWRKY9 module orchestrates ethylene-induced petal abscission via dual control of ROS homeostasis in rose. Sci. Adv. 2026, 12, eadu6821. DOI: 10.1126/sciadv.adu6821

[82]

Liang Y, Jiang C, Liu Y, Gao Y, Lu J, Aiwaili P, et al. Auxin regulates sucrose transport to repress petal abscission in rose (Rosa hybrida). Plant Cell 2020, 32, 3485-3499. DOI: 10.1105/tpc.19.00695

[83]

Gao Y, Liu C, Li X, Xu H, Liang Y, Ma N, et al. Transcriptome profiling of petal abscission zone and functional analysis of an Aux/IAA family gene RhIAA16 involved in petal shedding in rose. Front. Plant Sci. 2016, 7, 1375. DOI: 10.3389/fpls.2016.01375

[84]

Eugster CH, Märki‐Fischer E. The chemistry of rose pigments. Angew. Chem. Int. Ed. Engl. 1991, 30, 654-672. DOI: 10.1002/anie.199106541

[85]

Grotewold E. The genetics and biochemistry of floral pigments. Annu. Rev. Plant Biol. 2006, 57, 761-780. DOI: 10.1146/annurev.arplant.57.032905.105248

[86]

He G, Zhang R, Jiang S, Wang H, Ming F. The MYB transcription factor RcMYB1 plays a central role in rose anthocyanin biosynthesis. Hortic. Res. 2023, 10, uhad080. DOI: 10.1093/hr/uhad080

[87]

Yan Y, Zhao J, Lin S, Li M, Liu J, Raymond O, et al. Light-mediated anthocyanin biosynthesis in rose petals involves a balanced regulatory module comprising transcription factors RhHY5, RhMYB114a, and RhMYB3b. J. Exp. Bot. 2023, 74, 5783-5804. DOI: 10.1093/jxb/erad253

[88]

Ma M, Li R, Li Y, Dai W, Shang J, He Y, et al. Anthocyanin biosynthesis and transport synergistically modulated by RcMYB75 and RcGSTFL11 play a pivotal role in the feedforward loop in response to drought stress. Plant J. 2025, 121, e17240. DOI: 10.1111/tpj.17240

[89]

Wang H, Yang Y, Kang Y, Li M, Luo J, Liu X, et al. Key transcription regulators in the formation of yellow traits in rose petals. Plant Physiol. Biochem. 2025, 227, 110174. DOI: 10.1016/j.plaphy.2025.110174

[90]

Ma X, Li D, Cai J, Yang S, Wang D, Zhang Q, et al. Auxin response factor, RhARF8 contributes to rose flower color fading via regulating anthocyanin biosynthesis by directly activating RhCHSa/c promoter activity. Ornam. Plant Res. 2025, 5, e021. DOI: 10.48130/opr-0025-0019

[91]

Castillejo C, Waurich V, Wagner H, Ramos R, Oiza N, Muñoz P, et al. Allelic variation of MYB10 is the major force controlling natural variation in skin and flesh color in strawberry (Fragaria spp.) Fruit. Plant Cell 2020, 32, 3723-3749. DOI: 10.1105/tpc.20.00474

[92]

Jiu S, Guan L, Leng X, Zhang K, Haider MS, Yu X, et al. The role of VvMYBA2r and VvMYBA2w alleles of the MYBA2 locus in the regulation of anthocyanin biosynthesis for molecular breeding of grape (Vitis spp.) skin coloration. Plant Biotechnol. J. 2021, 19, 1216-1239. DOI: 10.1111/pbi.13543

[93]

Gao Y, Wang F, Xia P, Zhang J, Peng Z, Liu Z, et al. Light-induced m6A RNA modification regulates anthocyanin accumulation during rose petal coloration. Plant Physiol. 2026, 201, kiag082. DOI: 10.1093/plphys/kiag082

[94]

Muhlemann JK, Klempien A, Dudareva N. Floral volatiles: From biosynthesis to function. Plant Cell Environ. 2014, 37, 1936-1949. DOI: 10.1111/pce.12314

[95]

Baudino S, Caissard JC, Bergougnoux V, Jullien F, Magnard JL, Scalliet G, et al. Production and emission of volatile compounds by petal cells. Plant Signal. Behav. 2007, 2, 525-526. DOI: 10.4161/psb.2.6.4659

[96]

Bergougnoux V, Caissard JC, Jullien F, Magnard JL, Scalliet G, Cock JM, et al. Both the adaxial and abaxial epidermal layers of the rose petal emit volatile scent compounds. Planta 2007, 226, 853-866. DOI: 10.1007/s00425-007-0531-1

[97]

Guterman I, Shalit M, Menda N, Piestun D, Dafny-Yelin M, Shalev G, et al. Rose scent: Genomics approach to discovering novel floral fragrance-related genes. Plant Cell 2002, 14, 2325-2338. DOI: 10.1105/tpc.005207

[98]

Shalit M, Shafir S, Larkov O, Bar E, Kaslassi D, Adam Z, et al. Volatile compounds emitted by rose cultivars: Fragrance perception by man and honeybees. Isr. J. Plant Sci. 2004, 52, 245-255. DOI: 10.1560/P7G3-FT41-XJCP-1XFM

[99]

Feng L, Chen C, Li T, Wang M, Tao J, Zhao D, et al. Flowery odor formation revealed by differential expression of monoterpene biosynthetic genes and monoterpene accumulation in rose (Rosa rugosa Thunb.). Plant Physiol. Biochem. 2014, 75, 80-88. DOI: 10.1016/j.plaphy.2013.12.006

[100]

Farhi M, Lavie O, Masci T, Hendel-Rahmanim K, Weiss D, Abeliovich H, et al. Identification of rose phenylacetaldehyde synthase by functional complementation in yeast. Plant Mol. Biol. 2010, 72, 235-245. DOI: 10.1007/s11103-009-9564-0

[101]

Chen X, Baldermann S, Cao S, Lu Y, Liu C, Hirata H, et al. Developmental patterns of emission of scent compounds and related gene expression in roses of the cultivar Rosa × hybrida cv. ‘Yves Piaget’. Plant Physiol. Biochem. 2015, 87, 109-114. DOI: 10.1016/j.plaphy.2014.12.016

[102]

Helsper JPFG, Davies JA, Bouwmeester HJ, Krol AF, van Kampen MH. Circadian rhythmicity in emission of volatile compounds by flowers of Rosa hybrida L. cv. Honesty. Planta 1998, 207, 88-95. DOI: 10.1007/s004250050459

[103]

Hendel-Rahmanim K, Masci T, Vainstein A, Weiss D. Diurnal regulation of scent emission in rose flowers. Planta 2007, 226, 1491-1499. DOI: 10.1007/s00425-007-0582-3

[104]

Picone J, Clery R, Watanabe N, MacTavish H, Turnbull CN. Rhythmic emission of floral volatiles from Rosa damascena semperflorens cv. ‘Quatre Saisons’. Planta 2004, 219, 468-478. DOI: 10.1007/s00425-004-1250-5

[105]

Magnard JL, Roccia A, Caissard JC, Vergne P, Sun P, Hecquet R, et al. Biosynthesis of monoterpene scent compounds in roses. Science 2015, 349, 81-83. DOI: 10.1126/science.aab0696

[106]

Bai M, Wang M, Kou X, Xu X, Wei G, Feng L. The RrMYB4-RrTPS31 module regulates the synthesis of sesquiterpenoids in Rosa rugosa. Plant Physiol. Biochem. 2025, 229, 110708. DOI: 10.1016/j.plaphy.2025.110708

[107]

Bao M, Xu Y, Wei G, Bai M, Wang J, Feng L. The MYC gene RrbHLH105 contributes to salt stress-induced geraniol in rose by regulating trehalose-6-phosphate signalling. Plant Cell Environ. 2025, 48, 1947-1962. DOI: 10.1111/pce.15266

[108]

Roccia A, Hibrand-Saint Oyant L, Cavel E, Caissard JC, Machenaud J, Thouroude T, et al. Biosynthesis of 2-phenylethanol in rose petals is linked to the expression of one allele of RhPAAS. Plant Physiol. 2019, 179, 1064-1079. DOI: 10.1104/pp.18.01468

[109]

Li Y, Li R, Shang J, Zhao K, Sui Y, Liu Z, et al. A de novo-originated gene drives rose scent diversification. Cell 2025, 188, 6121-6137.e24. DOI: 10.1016/j.cell.2025.08.011

[110]

Wu S, Watanabe N, Mita S, Dohra H, Ueda Y, Shibuya M, et al. The key role of phloroglucinol O-methyltransferase in the biosynthesis of Rosa chinensis volatile 1,3,5-trimethoxybenzene. Plant Physiol. 2004, 135, 95-102. DOI: 10.1104/pp.103.037051

[111]

Liu X, Li D, Zhang S, Xu Y, Zhang Z. Genome-wide characterization of the rose (Rosa chinensis) WRKY family and role of RcWRKY41 in gray mold resistance. BMC Plant Biol. 2019, 19, 522. DOI: 10.1186/s12870-019-2139-6

[112]

Fang P, Arens P, Liu X, Zhang X, Lakwani D, Foucher F, et al. Analysis of allelic variants of RhMLO genes in rose and functional studies on susceptibility to powdery mildew related to clade V homologs. Theor. Appl. Genet. 2021, 134, 2495-2515. DOI: 10.1007/s00122-021-03838-7

[113]

Terefe-Ayana D, Yasmin A, Le TL, Kaufmann H, Biber A, Kühr A, et al. Mining disease-resistance genes in roses: Functional and molecular characterization of the rdr1 locus. Front. Plant Sci. 2011, 2, 35. DOI: 10.3389/fpls.2011.00035

[114]

Liu X, Zhou X, Li D, Hong B, Gao J, Zhang Z. Rose WRKY13 promotes disease protection to Botrytis by enhancing cytokinin content and reducing abscisic acid signaling. Plant Physiol. 2023, 191, 679-693. DOI: 10.1093/plphys/kiac495

[115]

Li D, Li X, Wang Z, Wang H, Gao J, Liu X, et al. Transcription factors RhbZIP17 and RhWRKY30 enhance resistance to Botrytis cinerea by increasing lignin content in rose petals. J. Exp. Bot. 2024, 75, 1633-1646. DOI: 10.1093/jxb/erad473

[116]

Li D, Liu X, Shu L, Zhang H, Zhang S, Song Y, et al. Global analysis of the AP2/ERF gene family in rose (Rosa chinensis) genome unveils the role of RcERF099 in Botrytis resistance. BMC Plant Biol. 2020, 20, 533. DOI: 10.1186/s12870-020-02740-6

[117]

Liu X, Cao X, Chen M, Li D, Zhang Z. Two transcription factors, RhERF005 and RhCCCH12, regulate rose resistance to Botrytis cinerea by modulating cytokinin levels. J. Exp. Bot. 2024, 75, 2584-2597. DOI: 10.1093/jxb/erae040

[118]

Ding C, Gao J, Zhang S, Jiang N, Su D, Huang X, et al. The basic/helix-loop-helix transcription factor family gene RcbHLH112 is a susceptibility gene in gray mold resistance of rose (Rosa Chinensis). Int. J. Mol. Sci. 2023, 24, 16305. DOI: 10.3390/ijms242216305

[119]

Li D, Li Z, Wang H, Jian R, Yang Y, Wang X, et al. Genome-wide and transcriptome analyses reveal RcCDPK5 as a positive regulator mediating resistance to Botrytis cinerea in Rosa chinensis. Ind. Crop. Prod. 2026, 240, 122666. DOI: 10.1016/j.indcrop.2026.122666

[120]

Liu X, Wang Z, Tian Y, Zhang S, Li D, Dong W, et al. Characterization of wall-associated kinase/wall-associated kinase-like (WAK/WAKL) family in rose (Rosa chinensis) reveals the role of RcWAK4 in Botrytis resistance. BMC Plant Biol. 2021, 21, 526. DOI: 10.1186/s12870-021-03307-9

[121]

Li X, He G, Jiang S, Yang C, Yang B, Ming F. Function of two splicing variants of RcCPR5 in the resistance of Rosa chinensis to powdery mildew. Plant Sci. 2023, 335, 111678. DOI: 10.1016/j.plantsci.2023.111678

[122]

Whitaker VM, Bradeen JM, Debener T, Biber A, Hokanson SC. Rdr3, a novel locus conferring black spot disease resistance in tetraploid rose: Genetic analysis, LRR profiling, and SCAR marker development. Theor. Appl. Genet. 2010, 120, 573-585. DOI: 10.1007/s00122-009-1177-0

[123]

Cheng H, Yang Y, Su L, Qi Y, Ji S, Liu T, et al. RcPsaL and RcPsbX, core photosystem subunits targeted by Marssonina rosae effector MrSEP20, enhance black spot resistance in rose. Plant Physiol. Biochem. 2025, 229, 110639. DOI: 10.1016/j.plaphy.2025.110639

[124]

Yang Y, Qi Y, Su L, Yang S, Yi X, Luo L, et al. The Marssonina rosae effector MrSEP43 suppresses immunity in rose by targeting the orphan protein RcBROG. J. Exp. Bot. 2024, 75, 4993-5007. DOI: 10.1093/jxb/erae200

[125]

Han Y, Tang A, Wan H, Zhang T, Cheng T, Wang J, et al. An APETALA2 homolog, RcAP2, regulates the number of rose petals derived from stamens and response to temperature fluctuations. Front. Plant Sci. 2018, 9, 481. DOI: 10.3389/fpls.2018.00481

[126]

Yang T, Wang Y, Li Y, Liang S, Yang Y, Huang Z, et al. The transcription factor RhMYB17 regulates the homeotic transformation of floral organs in rose (Rosa hybrida) under cold stress. J. Exp. Bot. 2024, 75, 2965-2981. DOI: 10.1093/jxb/erae099

[127]

Lu J, Wang W, Fan C, Sun J, Yuan G, Guo Y, et al. Telo boxes within the AGAMOUS second intron recruit histone 3 lysine 27 methylation to increase petal number in rose (Rosa chinensis) in response to low temperatures. Plant J. 2024, 118, 1486-1499. DOI: 10.1111/tpj.16691

[128]

Zaccai M, Ackerman R, Genis O, Riov J, Zik M. The bent peduncle phenomenon in roses is a developmental process involving auxin. Plant Sci. 2009, 176, 736-743. DOI: 10.1016/j.plantsci.2009.02.014

[129]

Qi W, Zhang C, Wang W, Cao Z, Li S, Li H, et al. Comparative transcriptome analysis of different heat stress responses between self-root grafting line and heterogeneous grafting line in rose. Hortic. Plant J. 2021, 7, 243-255. DOI: 10.1016/j.hpj.2021.03.004

[130]

Li ZQ, Xing W, Luo P, Zhang FJ, Jin XL, Zhang MH. Comparative transcriptome analysis of Rosa chinensis ‘Slater’s crimson China’ provides insights into the crucial factors and signaling pathways in heat stress response. Plant Physiol. Biochem. 2019, 142, 312-331. DOI: 10.1016/j.plaphy.2019.07.002

[131]

Sun Y, Li S, Wu X, Zhu J, Dong F, Pei Z, et al. Characterization and functional analysis of RhHsfA7, a heat stress transcription factor in roses (Rosa hybrid ‘Samantha’). Plants 2025, 14, 1155. DOI: 10.3390/plants14081155

[132]

Zhang J, Cao Y, Jin X, Zhang M, Wen Y, Li Z, et al. Integrated ATAC-seq and RNA-seq reveal RcHSF30 regulating sHSP and BAG for thermotolerance in rose. Ind. Crop. Prod. 2025, 233, 121440. DOI: 10.1016/j.indcrop.2025.121440

[133]

Zhang Y, Yu S, Niu P, Su L, Jiao X, Sui X, et al. RcMYB8 enhances salt and drought tolerance in rose (Rosa chinensis) by modulating RcPR5/1 and RcP5CS1. Mol. Hortic. 2024, 4, 3. DOI: 10.1186/s43897-024-00080-9

[134]

Geng L, Yu S, Zhang Y, Su L, Lu W, Zhu H, et al. Transcription factor RcNAC091 enhances rose drought tolerance through the abscisic acid-dependent pathway. Plant Physiol. 2023, 193, 1695-1712. DOI: 10.1093/plphys/kiad366

[135]

Chen JR, Chen YB, Ziemiańska M, Liu R, Deng ZN, Niedźwiecka-Filipiak I, et al. Co-expression of MtDREB1C and RcXET enhances stress tolerance of transgenic china rose (Rosa chinensis Jacq.). J. Plant Growth Regul. 2016, 35, 586-599. DOI: 10.1007/s00344-015-9564-z

[136]

Zang F, Wu Q, Li Z, Li L, Xie X, Tong B, et al. RrWRKY1, a transcription factor, is involved in the regulation of the salt stress response in rosa rugosa. Plants 2024, 13, 2973. DOI: 10.3390/plants13212973

[137]

Yang Z, Lin L, Lu M, Ma W, An H. A bHLH transcription factor RrUNE12 regulates salt tolerance and promotes ascorbate synthesis. Plant Cell Rep. 2025, 44, 42. DOI: 10.1007/s00299-025-03428-7

[138]

Su L, Zhang Y, Yu S, Geng L, Lin S, Ouyang L, et al. RcbHLH59-RcPRs module enhances salinity stress tolerance by balancing Na(+)/K(+) through callose deposition in rose (Rosa chinensis) . Hortic. Res. 2023, 10, uhac291. DOI: 10.1093/hr/uhac291

[139]

Yoshiba Y, Kiyosue T, Katagiri T, Ueda H, Mizoguchi T, Yamaguchi‐Shinozaki K, et al. Correlation between the induction of a gene for delta 1-pyrroline-5-carboxylate synthetase and the accumulation of proline in Arabidopsis thaliana under osmotic stress. Plant. J. 1995, 7, 751-760. DOI: 10.1046/j.1365-313X.1995.07050751.x

[140]

Teng Y, Lv M, Zhang X, Cai M, Chen T. BEAR1, a bHLH transcription factor, controls salt response genes to regulate rice salt response. J. Plant Biol. 2022, 65, 217-230. DOI: 10.1007/s12374-022-09347-4

[141]

Zhang S, Feng M, Chen W, Zhou X, Lu J, Wang Y, et al. In rose, transcription factor PTM balances growth and drought survival via PIP2;1 aquaporin. Nat. Plants 2019, 5, 290-299. DOI: 10.1038/s41477-019-0376-1

[142]

Shen Y, Zou J, Zhang Q, Luo P, Shang W, Sun T, et al. Identification of PP2Cs in six rosaceae species highlights RcPP2C24 as a negative regulator in rose drought tolerance. Plant Physiol. Biochem. 2024, 212, 108782. DOI: 10.1016/j.plaphy.2024.108782

[143]

Shang X, Xie N, Li Y, Zhao Z, Luo P, Cui Y, et al. Mediator subunit RhMED15a regulates drought tolerance in rose. Horticulturae 2024, 10, 84. DOI: 10.3390/horticulturae10010084

[144]

Xie N, Shi H, Shang X, Zhao Z, Fang Y, Wu H, et al. RhMED15a-like, a subunit of the mediator complex, is involved in the drought stress response in Rosa hybrida. BMC Plant Biol. 2024, 24, 351. DOI: 10.1186/s12870-024-05059-8

[145]

Zhao Q, Jing W, Fu X, Yang R, Zhu C, Zhao J, et al. TSPO-induced degradation of the ethylene receptor RhETR3 promotes salt tolerance in rose (Rosa hybrida). Hortic. Res. 2024, 11, uhae040. DOI: 10.1093/hr/uhae040

[146]

Dai F, Zhang C, Jiang X, Kang M, Yin X, Lü P, et al. RhNAC2 and RhEXPA4 are involved in the regulation of dehydration tolerance during the expansion of rose petals. Plant Physiol. 2012, 160, 2064-2082. DOI: 10.1104/pp.112.207720

[147]

Jiang X, Zhang C, Lü P, Jiang G, Liu X, Dai F, et al. RhNAC3, a stress-associated NAC transcription factor, has a role in dehydration tolerance through regulating osmotic stress-related genes in rose petals. Plant Biotechnol. J. 2014, 12, 38-48. DOI: 10.1111/pbi.12114

[148]

Zou J, Lü P, Jiang L, Liu K, Zhang T, Chen J, et al. Regulation of rose petal dehydration tolerance and senescence by RhNAP transcription factor via the modulation of cytokinin catabolism. Mol. Hortic. 2021, 1, 13. DOI: 10.1186/s43897-021-00016-7

[149]

Luo P, Zhang H, Chen Y, Cui Y, Chen W. RhbHLH92 positively regulates the dehydration tolerance by interacting with RhMYB123 in rose petals (Rosa hybrida). Environ. Exp. Bot. 2024, 228, 106049. DOI: 10.1016/j.envexpbot.2024.106049

[150]

Liu K, Zhang T, Zhao S, Chen J, Zhou W, Chen S, et al. Scaffold protein RhCASPL1D1 stabilizes RhPIP2 aquaporins and promotes flower recovery after dehydration in rose (Rosa hybrida). Hortic. Res. 2015, 12, uhaf119. DOI: 10.1093/hr/uhaf119

[151]

Meng Y, Ma N, Zhang Q, You Q, Li N, Ali Khan M, et al. Precise spatio-temporal modulation of ACC synthase by MPK6 cascade mediates the response of rose flowers to rehydration. Plant J. 2014, 79, 941-950. DOI: 10.1111/tpj.12594

[152]

Chen J, Zhang Q, Wang Q, Feng M, Li Y, Meng Y, et al. RhMKK9, a rose MAP KINASE KINASE gene, is involved in rehydration-triggered ethylene production in rose gynoecia. BMC Plant Biol. 2017, 17, 51. DOI: 10.1186/s12870-017-0999-1

[153]

Zhou N, Simonneau F, Thouroude T, Oyant LHS, Foucher F. Morphological studies of rose prickles provide new insights. Hortic. Res. 2021, 8, 221. DOI: 10.1038/s41438-021-00689-7

[154]

Kumari P, Gangwar H, Gahlaut V, Kumari P, Jaiswal V. Identification of a natural RcLOG1 allele linked to prickle development in Rose (Rosa spp.). Planta 2025, 262, 101. DOI: 10.1007/s00425-025-04817-8

[155]

Lee KY, Lee SY, Kim YJ, Choi YJ, Lim SH, Kang YI. Overexpression of VtF3′5′H and RhNHX genes alters flower color and plant morphology in transgenic rose ‘Red Farm’. Plants 2025, 14, 3185. DOI: 10.3390/plants14203185

[156]

Zeng H, Zhou SZ, Zhang HL, Zhao BY, Liu YL, Zeng YH, et al. Pan-plantae aquaporin evolution: insights into PIP2 as a potential regulator of rose prickle development. Hortic. Res. 2016, uhag143. DOI: 10.1093/hr/uhag143

[157]

Zhou NN, Tang KX, Jeauffre J, Thouroude T, Arias DCL, Foucher F, et al. Genetic determinism of prickles in rose. Theor. Appl. Genet. 2020, 133, 3017-3035. DOI: 10.1007/s00122-020-03652-7

[158]

Steinberger AR, Voytas DF. Virus-induced gene editing free from tissue culture. Nat. Plants 2025, 11, 1241-1251. DOI: 10.1038/s41477-025-02025-6

PDF (1108KB)

8

Accesses

0

Citation

Detail

Sections
Recommended

/

〈 〉