Transcriptomic and physiological analysis identifies a gene network module highly associated with brassinosteroid regulation in hybrid sweetgum tissues differing in the capability of somatic embryogenesis

Ruirui Zhao , Shuaizheng Qi , Ying Cui , Ying Gao , Shuaifei Jiang , Jian Zhao , Jinfeng Zhang , Lisheng Kong

Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) : uhab047

PDF (1863KB)
Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) :uhab047 DOI: 10.1093/hr/uhab047
Article
research-article
Transcriptomic and physiological analysis identifies a gene network module highly associated with brassinosteroid regulation in hybrid sweetgum tissues differing in the capability of somatic embryogenesis
Author information +
History +
PDF (1863KB)

Abstract

Somatic embryogenesis is a preferred method for large-scale production of forest trees due to its high propagation efficiency. In this study, hybrid sweetgum leaves with phase changes from mature to embryogenic state were selected as experimental material to study somatic embryo initiation. Embryogenicity ranged from high to low, i.e. from 45%, 25%, and 12.5% to 0, with the samples of embryogenic callus (EC), whiten leaf edge (WLI), whiten leaf (WLII), and green leaf (GL) respectively. High correlations existed between embryogenicity and endogenous brassinosteroids (BRs) (r = 0.95, p < 0.05). Similarly, concentrations of endogenous BRs of the sample set correlated positively (r = 0.93, 0.99, 0.87, 0.99, 0.96 respectively, P < 0.05) to expression of somatic embryo (SE)-related genes, i.e. BBM, LEC2, ABI3, PLT2, and WOX2. Hierarchical cluster and weighted gene coexpression network analysis identified modules of coexpressed genes and network in 4820 differentially expressed genes (DEGs) from All-BR-Regulated Genes (ABRG). Moreover, exogenously-supplemented epiBR, together with 2,4-D and 6-BA, increased embryogenicity of GL-sourced callus, and expression of SE- and auxin-related genes, while brassinazole (BRZ), a BR biosynthesis inhibitor, reduced embryogenicity. Evidences obtained in this study revealed that BRs involved in phase change of leaf explants and may function in regulating gene expression and enhancing auxin effects. This study successfully established protocols for inducing somatic embryogenesis from leaf explants in hybrid sweetgum, which could facilitate the propagation process greatly, and provide theoretical basis for manipulating SE competence of explants in ornamental woody plants.

Cite this article

Download citation ▾
Ruirui Zhao, Shuaizheng Qi, Ying Cui, Ying Gao, Shuaifei Jiang, Jian Zhao, Jinfeng Zhang, Lisheng Kong. Transcriptomic and physiological analysis identifies a gene network module highly associated with brassinosteroid regulation in hybrid sweetgum tissues differing in the capability of somatic embryogenesis. Horticulture Research, 2022, 9 (1) : uhab047 DOI:10.1093/hr/uhab047

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Songstad DD, Petolino JF, Voytas DF et al. Genome editing of plants. Crit Rev Plant Sci. 2017; 36: 1-23.

[2]

Florez SL, Erwin RL, Maximova SN et al. Enhanced somatic embryogenesis in Theobroma cacao using the homologous BABY BOOM transcription factor. BMC Plant Biol. 2015; 15: 121.

[3]

Iwase A, Mita K, Nonaka S et al. WIND1-based acquisition of regeneration competency in Arabidopsis and rapeseed. J Plant Res. 2015; 128: 389-97.

[4]

Pérez-Pascual D, Jiménez-Guillen D, Villanueva-Alonzo H et al. Ectopic expression of the Coffea canephora SERK1 homolog-induced differential transcription of genes involved in auxin metabolism and in the developmental control of embryogenesis. Physiol Plant. 2018; 163: 530-51.

[5]

Shiota H, Satoh R, Watabe K-i et al. C-ABI3, the carrot homologue of the Arabidopsis ABI3, is expressed during both zygotic and somatic embryogenesis and functions in the regulation of embryo-specific ABA-inducible genes. Plant Cell Physiol. 1998; 39: 1184-93.

[6]

Zheng Y, Ren N, Wang H et al. Global identification of targets of the Arabidopsis MADS domain protein AGAMOUS-like15. Plant Cell. 2009; 21: 2563-77.

[7]

Arroyo HA, Ku-González A, Canche R et al. Expression of WUSCHEL in Coffea canephora causes ectopic morphogenesis and increases somatic embryogenesis. Plant Cell Tissue Organ Cult. 2008; 94: 171-80.

[8]

Xiao YQ, Chen YL, Ding YP et al. Effects of GhWUS from upland cotton (Gossypium hirsutum L.) on somatic embryogenesis and shoot regeneration. Plant Sci. 2018; 270: 157-65.

[9]

Merkle S, Montello P, Kormanik T et al. Propagation of novel hybrid sweetgum phenotypes for ornamental use via somatic embryogenesis. Propag Ornam Plants. 2010; 10: 220-6.

[10]

Merkle SA, Neu KA, Battle PJ et al. Somatic embryogenesis and plantlet regeneration from immature and mature tissues of sweetgum (Liquidambar styraciflua) . Plant Sci. 1998; 132: 169-78.

[11]

Haberlandt G . In: Laimer M, Rücker W, eds. Plant Tissue Culture . Springer, 2003, 1-24.

[12]

Corredoira E, Merkle SA, Martínez MT et al. Non-zygotic embryogenesis in hardwood species. CRC Crit Rev Plant Sci. 2019; 38: 29-97.

[13]

Merkle SA, Battle PJ . Enhancement of embryogenic culture initiation from tissues of mature sweetgum trees. Plant Cell Rep. 2000; 19: 268-73.

[14]

Vendrame WA, Holliday CP, Merkle SA . Clonal propagation of hybrid sweetgum (Liquidambar styraciflua × L. formosana) by somatic embryogenesis. Plant Cell Rep. 2001; 20: 691-5.

[15]

von Aderkas P, Bonga J . Influencing micropropagation and somatic embrygenesis in mature trees by manipulation of phase change, stress and culture environment. Tree Physiol. 2000; 20: 921-8.

[16]

Xie ZL, Nolan T, Jiang H et al. The AP2/ERF transcription factor TINY modulates brassinosteroid-regulated plant growth and drought responses in Arabidopsis. Plant Cell. 2019; 31: 1788-806.

[17]

Cheng YW, Zhu WJ, Chen YX et al. Brassinosteroids control root epidermal cell fate via direct regulation of a MYB-bHLH-WD40 complex by GSK3-like kinases. elife. 2014; 25: e02525.

[18]

Li ZC, He YH . Roles of brassinosteroids in plant reproduction. Int J Mol Sci. 2020; 21: 872.

[19]

Azpeitia A, Chan JL, Saenz L et al. Effect of 22(S),23(S)-homobrassinolide on somatic embryogenesis in plumule explants of Cocos nucifera (L.) cultured in vitro. J Hortic Sci Biotechnol. 2003; 78: 591-6.

[20]

Chone RM, Rocha DI, Monte-Bello CC et al. Brassinosteroid increases the cytokinin efficiency to induce direct somatic embryogenesis in leaf explants of Coffea arabica L. Plant Cell Tissue Organ Cult. 2018; 135: 63-71.

[21]

Sasaki H. Brassinolide promotes adventitious shoot regeneration from cauliflower hypocotyl segments. Plant Cell Tissue Organ Cult. 2002; 71: 111-6.

[22]

Núñez M, Siqueira WJ, Hernández M et al. Effect of spirostane analogues of brassinosteroids on callus formation and plant regeneration in lettuce (Lactuca sativa) . Plant Cell Tissue Organ Cult. 2004; 78: 97-9.

[23]

Aydin Y, Ogras T, Ipekçi-Altas Z et al. Effects of brassinosteroid on cotton regeneration via somatic embryogenesis. Biologia. 2006; 61: 289-93.

[24]

Wang ZY, Bai MY, Oh E et al. Brassinosteroid signaling network and regulation of photomorphogenesis. Annu Rev Genet. 2012; 46: 701-24.

[25]

Nakamura A, Goda H, Shimada Y et al. Brassinosteroid selectively regulates PIN gene expression in Arabidopsis. Biosci Biotechnol Biochem. 2004; 68: 952-4.

[26]

Kim TW, Lee SM, Joo SH et al. Elongation and gravitropic responses of Arabidopsis roots are regulated by brassinolide and IAA. Plant Cell Environ. 2007; 30: 679-89.

[27]

Nakamura A, Higuchi K, Goda H et al. Brassinolide induces IAA5, IAA19, and DR5, a synthetic auxin response element in Arabidopsis, implying a cross talk point of brassinosteroid and auxin signaling . Plant Physiol. 2003; 133: 1843-53.

[28]

Kim H, Park PJ, Hwang HJ et al. Brassinosteroid signals control expression of the AXR3/IAA17 gene in the cross-talk point with auxin in root development. Biosci Biotechnol Biochem. 2006; 70: 768-73.

[29]

Sun Y, Fan XY, Cao DM et al. Integration of brassinosteroid signal transduction with the transcription network for plant growth regulation in Arabidopsis. Dev Cell. 2010; 19: 765-77.

[30]

Chen LG, Gao ZH, Zhao ZY et al. BZR1 family transcription factors function redundantly and indispensably in BR signaling but exhibit BIR1-independent function in regulating anther development in arabidopsis. Mol Plant. 2019; 12: 1408-15.

[31]

Zhang Z, Sun Y, Li Y . Plant rejuvenation: from phenotypes to mechanisms. Plant Cell Rep. 2020; 39: 1249-62.

[32]

Zuo JR, Niu QW, Frugis G et al. The WUSCHEL gene promotes vegetative-to-embryonic transition in Arabidopsis . Plant J. 2002; 30: 349-59.

[33]

Boutilier K, Offringa R, Sharma VK et al. Ectopic expression of BABY BOOM triggers a conversion from vegetative to embryonic growth. Plant Cell. 2002; 14: 1737-49.

[34]

Tsuwamoto R, Yokoi S, Takahata Y . Arabidopsis embryomaker encoding an AP2 domain transcription factor plays a key role in developmental change from vegetative to embryonic phase. Plant Mol Biol. 2010; 73: 481-92.

[35]

Li K, Wang J, Liu C et al. Expression of AtLEC2 and AtIPTs promotes embryogenic callus formation and shoot regeneration in tobacco . BMC Plant Biol. 2019; 19: 314.

[36]

Gazzarrini S, Tsuchiya Y, Lumba S et al. The transcription factor FUSCA3 controls developmental timing in Arabidopsis through the hormones gibberellin and abscisic acid . Dev Cell. 2004; 7: 373-85.

[37]

Horstman A, Li M, Heidmann I et al. The baby boom transcription factor activates the lec1-abi3-fus3-lec2 network to induce somatic embryogenesis. Plant Physiol. 2017; 175: 848-57.

[38]

González-García MP, Vilarrasa-Blasi J, Zhiponova M et al. Brassinosteroids control meristem size by promoting cell cycle progression in Arabidopsis roots. Development. 2011; 138: 849-59.

[39]

Kareem A, Durgaprasad K, Sugimoto K et al. PLETHORA genes control regeneration by a two-step mechanism. Curr Biol. 2015; 25: 1017-30.

[40]

Aida M, Ishida T, Fukaki H et al. Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant. Plant Cell. 1997; 9: 841-57.

[41]

Nakamura A, Nakajima N, Goda H et al. Arabidopsis aux/IAA genes are involved in brassinosteroid-mediated growth responses in a manner dependent on organ type. Plant J. 2006; 45: 193-205.

[42]

Bao F, Shen J, Brady S et al. Brassinosteroids interact with auxin to promote lateral root development in Arabidopsis. Plant Physiol. 2004; 134: 1624-31.

[43]

Li L, Xu J, Xu ZH et al. Brassinosteroids stimulate plant tropisms through modulation of polar auxin transport in brassica and Arabidopsis . Plant Cell. 2005; 17: 2738-53.

[44]

Sun RB, Wang SH, Ma D et al. Genome-wide analysis of cotton auxin early response gene families and their roles in somatic embryogenesis. Genes (Basel). 2019; 10: 730.

[45]

Chen Q, Dai X, De-Paoli H et al. Auxin overproduction in shoots cannot rescue auxin deficiencies in Arabidopsis roots. Plant Cell Physiol. 2014; 55: 1072-9.

[46]

Wang Y, Li B, Du MW et al. Mechanism of phytohormone involvement in feedback regulation of cotton leaf senescence induced by potassium deficiency. J Exp Bot. 2012; 63: 5887-901.

[47]

Langfelder P, Horvath S . WGCNA: an R package for weighted correlation network analysis. BMC Bioinformatics. 2008; 9: 559.

[48]

Shannon P, Markiel A, Ozier O et al. Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res. 2003; 13: 2498-504.

PDF (1863KB)

31

Accesses

0

Citation

Detail

Sections
Recommended

/