Integrated transcriptome and proteome analysis reveals brassinosteroid-mediated regulation of cambium initiation and patterning in woody stem

Congpeng Wang , Naixu Liu , Zhao Geng , Meijing Ji , Shumin Wang , Yamei Zhuang , Dian Wang , Guo He , Shutang Zhao , Gongke Zhou , Guohua Chai

Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) : uhab048

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Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) :uhab048 DOI: 10.1093/hr/uhab048
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Integrated transcriptome and proteome analysis reveals brassinosteroid-mediated regulation of cambium initiation and patterning in woody stem
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Abstract

Wood formation involves sequential developmental events requiring the coordination of multiple hormones. Brassinosteroids (BRs) play a key role in wood development, but little is known about the cellular and molecular processes that underlie wood formation in tree species. Here, we generated transgenic poplar lines with edited PdBRI1 genes, which are orthologs of Arabidopsis vascular-enriched BR receptors, and showed how inhibition of BR signaling influences wood development at the mRNA and/or proteome level. Six Populus PdBRI1 genes formed three gene pairs, each of which was highly expressed in basal stems. Simultaneous mutation of PdBRI1–1, − 2, − 3 and − 6, which are orthologs of the Arabidopsis vascular-enriched BR receptors BRI1, BRL1 and BRL3, resulted in severe growth defects. In particular, the stems of these mutant lines displayed a discontinuous cambial ring and patterning defects in derived secondary vascular tissues. Abnormal cambial formation within the cortical parenchyma was also observed in the stems of pdbri1–1;2;3;6. Transgenic poplar plants expressing edited versions of PdBRI1–1 or PdBRI1–1;2;6 exhibited phenotypic alterations in stem development at 4.5 months of growth, indicating that there is functional redundancy among these PdBRI1 genes. Integrated analysis of the transcriptome and proteome of pdbri1–1;2;3;6 stems revealed differential expression of a number of genes/proteins associated with wood development and hormones. Concordant (16%) and discordant (84%) regulation of mRNA and protein expression, including wood-associated mRNA/protein expression, was found in pdbri1–1;2;3;6 stems. This study found a dual role of BRs in procambial cell division and xylem differentiation and provides insights into the multiple layers of gene regulation that contribute to wood formation in Populus.

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Congpeng Wang, Naixu Liu, Zhao Geng, Meijing Ji, Shumin Wang, Yamei Zhuang, Dian Wang, Guo He, Shutang Zhao, Gongke Zhou, Guohua Chai. Integrated transcriptome and proteome analysis reveals brassinosteroid-mediated regulation of cambium initiation and patterning in woody stem. Horticulture Research, 2022, 9 (1) : uhab048 DOI:10.1093/hr/uhab048

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References

[1]

Plomion C, Leprovost G, Stokes A . Wood formation in trees. Plant Physiol. 2001; 127: 1513-23.

[2]

Zhang J, Elo A, Helariutta Y . Arabidopsis as a model for wood formation. Curr Opin Biotech. 2011; 22: 293-9.

[3]

Jin H, Do J, Shin SJ et al. Exogenously applied 24-epi brassinolide reduces lignification and alters cell wall carbohydrate biosynthesis in the secondary xylem of Liriodendron tulipifera . Phytochemistry. 2014; 101: 40-51.

[4]

Noh SA, Choi YI, Cho JS et al. The poplar basic helix-loop-helix transcription factor BEE3-like gene affects biomass production by enhancing proliferation of xylem cells in poplar. Biochem Biophys Res Commun. 2015; 462: 64-70.

[5]

Jin YL, Tang RJ, Wang HH et al. Overexpression of Populus trichocarpa CYP85A3 promotes growth and biomass production in transgenic trees. Plant Biotechnol J. 2017; 15: 1309-21.

[6]

Du J, Gerttula S, Li Z et al. Brassinosteroid regulation of wood formation in poplar. New Phytol. 2020; 225: 1516-30.

[7]

Wang W, Bai MY, Wang ZY . The brassinosteroid signaling network-a paradigm of signal integration. Curr Opin Plant Biol. 2014; 21: 147-53.

[8]

Lozano-Elena F, Cano-Delgado A . Emerging roles of vascular brassinosteroid receptors of the BRI1-like family. Curr Opin Plant Biol. 2019; 51: 105-13.

[9]

Nolan TM, Vukašinović N, Liu D et al. Brassinosteroids: multidimensional regulators of plant growth, development, and stress responses. Plant Cell. 2020; 32: 295-318.

[10]

Szekeres M, Nemeth K, Kalman ZK et al. Brassinosteroids rescue the deficiency of CYP90, a cytochrome P450, controlling cell elongation and de-etiolation in Arabidopsis. Cell. 1996; 85: 171-82.

[11]

Li J, Chory J . A putative leucine-rich repeat receptor kinase involved in brassinosteroid signal transduction. Cell. 1997; 90: 929-38.

[12]

Ibanes M, Fabregas N, Chory J et al. A.I. Brassinosteroid signaling and auxin transport are required to establish the periodic pattern of Arabidopsis shoot vascular bundles. Proc Natl Acad Sci U S A. 2009; 106: 13630-5.

[13]

Kondo Y, Lto T, Nakagami H et al. Plant GSK3 proteins regulate xylem cell differentiation downstream of TDIF-TDR signalling. Nat Commun. 2014; 5: 3504.

[14]

Wang JP, Matthews ML, Williams CM et al. Improving wood properties for wood utilization through multi-omics integration in lignin biosynthesis. Nat Commun. 2018; 9: 1579.

[15]

Caño-Delgado A, Yin Y, Yu C et al. BRL1 and BRL3 are novel brassinosteroid receptors that function in vascular differentiation in Arabidopsis . Development. 2004; 131: 5341-51.

[16]

Li E, Bhargava A, Qiang W et al. The class II KNOX gene KNAT7 negatively regulates secondary wall formation in Arabidopsis and is functionally conserved in Populus. New Phytol. 2012; 194: 102-15.

[17]

Minic Z, Rihouey C, Do CT et al. Purification and characterization of enzymes exhibiting β-D-xylosidase activities in stem tissues of Arabidopsis. Plant Physiol. 2004; 135: 867-78.

[18]

Siedlecka A, Wiklund S, Peronne MA et al. Pectin methyl esterase inhibits intrusive and symplastic cell growth in developing wood cells of Populus. Plant Physiol. 2008; 146: 554-65.

[19]

Zhang J, Tuskan GA, Tschaplinski TJ et al. Transcriptional and post-transcriptional regulation of lignin biosynthesis pathway genes in Populus . Front Plant Sci. 2020; 11: 652.

[20]

Agusti J, Herold S, Schwarz M et al. Strigolactone signaling is required for auxin-dependent stimulation of secondary growth in plants. Proc Natl Acad Sci U S A. 2011; 108: 20242-7.

[21]

Schrader J, Baba K, May ST et al. Polar auxin transport in the wood-forming tissues of hybrid aspen is under simultaneous control of developmental and environmental signals. Proc Natl Acad Sci U S A. 2003; 100: 10096-101.

[22]

Lu S, Li Q, Wei H et al. Ptr-miR397a is a negative regulator of laccase genes affecting lignin content in Populus trichocarpa . Proc Natl Acad Sci U S A. 2013; 110: 10848-53.

[23]

Berthet S, Demont-Caulet N, Pollet B et al. Disruption of LACCASE4 and 17 results in tissue-specific alterations to lignification of Arabidopsis thaliana stems. Plant Cell. 2011; 23: 1124-37.

[24]

Zhao Q, Nakashima J, Chen F et al. Laccase is necessary and nonredundant with peroxidase for lignin polymerization during vascular development in Arabidopsis. Plant Cell. 2013; 25: 3976-87.

[25]

Takei K, Yamaya T, Sakakibara H . Arabidopsis CYP735A1 and CYP735A2 encode cytokinin hydroxylases that catalyze the biosynthesis of trans-zeatin. J Biol Chem. 2004; 279: 41866-72.

[26]

Miyawaki K, Tarkowski P, Matsumoto-Kitano M et al. Roles of Arabidopsis ATP/ADP isopentenyltransferases and tRNA isopentenyltransferases in cytokinin biosynthesis. Proc Natl Acad Sci U S A. 2006; 103: 16598-603.

[27]

Werner T, Motyka V, Laucou V et al. Cytokinin-deficient transgenic Arabidopsis plants show multiple developmental alterations indicating opposite functions of cytokinins in the regulation of shoot and root meristem activity. Plant Cell. 2003; 15: 2532-50.

[28]

Kuroha T, Tokunaga H, Kojima M et al. Functional analyses of LONELY GUY cytokinin-activating enzymes reveal the importance of the direct activation pathway in Arabidopsis. Plant Cell. 2009; 21: 3152-69.

[29]

Seyfferth C, Wessels B, Jokipii-Lukkari S et al. Ethylene-related gene expression networks in wood formation. Front Plant Sci. 2018; 9: 272.

[30]

Etchells JP, Provost CM, Turner ST . Plant vascular cell division is maintained by an interaction between PXY and ethylene signalling. PLoS Genet. 2012; 8: e1002997.

[31]

Nilsson J, Karlberg A, Antti H et al. Dissecting the molecular basis of the regulation of wood formation by auxin in hybrid aspen. Plant Cell. 2008; 20: 843-55.

[32]

Nieminen K, Immanen J, Laxell M et al. Cytokinin signaling regulates cambial development in poplar. Proc Nat Acad Sc U S. 2008; 105: 20032-7.

[33]

Love J, Bjorklund S, Vahala J et al. Ethylene is an endogenous stimulator of cell division in the cambial merstem of Populus . Proc Nat Acad Sc U S. 2009; 106: 5984-9.

[34]

Jouannet V, Brackmann K, Greb T . (pro)cambium formation and proliferation: two sides of the same coin? Curr Opin Plant Biol. 2015; 23: 54-60.

[35]

Hardtke CS, Berleth T . The Arabidopsis gene MONOPTEROS encodes a transcription factor mediating embryo axis formation and vascular development. EMBO J. 1998; 17: 1405-11.

[36]

Bishopp A, Help H, El-Showk S et al. A mutually inhibitory interaction between auxin and cytokinin specifies vascular pattern in roots. Curr Biol. 2011; 21: 917-26.

[37]

Yamamoto R, Demura T, Fukuda H . Brassinosteroids induce entry into the final stage of tracheary element differentiation in cultured Zinnia cells. Plant Cell Physiol. 1997; 38: 980-3.

[38]

Jamet E, Roujol D, San-Clemente H et al. Cell wall biogenesis of Arabidopsis thaliana elongating cells: transcriptomics complements proteomics. BMC Genomics. 2009; 10: 505.

[39]

Zhao Q, Chen W, Bian J et al. Proteomics and phosphoproteomics of heat stress-responsive mechanisms in spinach. Front Plant Sci. 2018; 9: 800.

[40]

Xu X, Liu X, Yan Y et al. Comparative proteomic analysis of cucumber powdery mildew resistance between a single-segment substitution line and its recurrent parent. Hortic Res. 2019; 6: 115.

[41]

Tuskan GA, Difazio S, Jansson S et al. The genome of black cottonwood, Populus trichocarpa (Torr. & Gray) . Science. 2006; 313: 1596-604.

[42]

Tang X, Wang D, Liu Y et al. Dual regulation of xylem formation by an auxin-mediated PaC3H17-PaMYB199 module in Populus . New Phytol. 2020; 225: 1545-61.

[43]

Schmittgen TD, Livak KJ . Analyzing real-time PCR data by the comparative C-T method. Nat Protoc. 2008; 3: 1101-8.

[44]

Ma X, Liu YG . CRISPR/Cas9-based multiplex genome editing in monocot and dicot plants. Curr Protoc Mol Biol. 2016; 115: 31.6.1-31.6.21.

[45]

Kim D, Langmead B, Salzberg S . HISAT: a fast spliced aligner with low memory requirements. Nat Methods. 2015; 12: 357-60.

[46]

Sturn A, Quackenbush J, Trajanoski Z . Genesis: cluster analysis of microarray data. Bioinformatics. 2002; 18: 207-8.

[47]

Wisniewski JR, Zougman A, Nagaraj N et al. Universal sample preparation method for proteome analysis. Nat Methods. 2009; 6: 359-62.

[48]

Futcher B, Latter GI, Monardo P et al. A sampling of the yeast proteome. Mol Cell Biol. 1999; 19: 7357-68.

[49]

Peterson AC, Russell JD, Bailey DJ et al. Parallel reaction monitoring for high resolution and high mass accuracy quantitative, targeted proteomics. Mol Cell Proteomics. 2012; 11: 1475-88.

[50]

MacLean B, Tomazela DM, Shulman N et al. Skyline: an open source document editor for creating and analyzing targeted proteomics experiments. Bioinformatics. 2010; 26: 966-8.

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