Overexpression of PvWOX3a in switchgrass promotes stem development and increases plant height

Ruijuan Yang , Zhenying Wu , Chen Bai , Zhichao Sun , Mengqi Wang , Yuzhu Huo , Hailing Zhang , Yamei Wang , Huapeng Zhou , Shaojun Dai , Wenwen Liu , Chunxiang Fu

Horticulture Research ›› 2021, Vol. 8 ›› Issue (1) : 252

PDF (1672KB)
Horticulture Research ›› 2021, Vol. 8 ›› Issue (1) :252 DOI: 10.1038/s41438-021-00678-w
Article
research-article
Overexpression of PvWOX3a in switchgrass promotes stem development and increases plant height
Author information +
History +
PDF (1672KB)

Abstract

Switchgrass (Panicum virgatum L.) is an important perennial, noninvasive, tall ornamental grass that adds color and texture to gardens and landscapes. Moreover, switchgrass has been considered a forage and bioenergy crop because of its vigorous growth, low-input requirements, and broad geography. Here, we identified PvWOX3a from switchgrass, which encodes a WUSCHEL-related homeobox transcription factor. Transgenic overexpression of PvWOX3a in switchgrass increased stem length, internode diameter, and leaf blade length and width, all of which contributed to a 95% average increase in dry weight biomass compared with control plants. Yeast one-hybrid and transient dual-luciferase assays showed that PvWOX3a can repress the expression of gibberellin 2-oxidase and cytokinin oxidase/dehydrogenase through apparently direct interaction with their promoter sequences. These results suggested that overexpression of PvWOX3a could increase gibberellin and cytokinin levels in transgenic switchgrass plants, which promotes cell division, elongation, and vascular bundle development. We also overexpressed PvWOX3a in a transgenic miR156-overexpressing switchgrass line that characteristically exhibited more tillers, thinner internodes, and narrower leaf blades. Double transgenic switchgrass plants displayed significant increases in internode length and diameter, leaf blade width, and plant height but retained a tiller number comparable to that of plants expressing miR156 alone. Ultimately, the double transgenic switchgrass plants produced 174% more dry-weight biomass and 162% more solubilized sugars on average than control plants. These findings indicated that PvWOX3a is a viable potential genetic target for engineering improved shoot architecture and biomass yield of horticulture, fodder, and biofuel crops.

Cite this article

Download citation ▾
Ruijuan Yang, Zhenying Wu, Chen Bai, Zhichao Sun, Mengqi Wang, Yuzhu Huo, Hailing Zhang, Yamei Wang, Huapeng Zhou, Shaojun Dai, Wenwen Liu, Chunxiang Fu. Overexpression of PvWOX3a in switchgrass promotes stem development and increases plant height. Horticulture Research, 2021, 8 (1) : 252 DOI:10.1038/s41438-021-00678-w

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Traas, J . Organogenesis at the shoot apical meristem. Plants 8, 6 (2018).

[2]

Pant, B. D., Buhtz, A., Kehr, J. & Scheible, W. R. MicroRNA399 is a long-distance signal for the regulation of plant phosphate homeostasis. Plant J. 53, 731-738 (2008).

[3]

Shiratake, K., Notaguchi, M., Makino, H., Sawai, Y. & Borghi, L. Petunia PLEIOTROPIC DRUG RESISTANCE 1 is a strigolactone short-distance transporter with long-distance outcomes. Plant Cell Physiol. 60, 1722-1733 (2019).

[4]

Yadav, R. K. & Reddy, G. V. WUSCHEL protein movement and stem cell homeostasis. Plant Signal. Behav. 7, 592-594 (2012).

[5]

Liu, Y. et al. MiR396-GRF module associates with switchgrass biomass yield and feedstock quality. Plant Biotechnol. J. https://doi.org/10.1111/pbi.13567 (2021).

[6]

Lorenzo, C. D. et al. Improvement of alfalfa forage quality and management through the down-regulation of MsFTa1. Plant Biotechnol. J. 18, 944-954 (2020).

[7]

Wuddineh, W. A. et al. Identification and overexpression of gibberellin 2-oxidase (GA2ox) in switchgrass (Panicum virgatum L.) for improved plant architecture and reduced biomass recalcitrance. Plant Biotechnol. J. 13, 636-647 (2015).

[8]

Wang, H. et al. Overexpression of the WOX gene STENOFOLIA improves biomass yield and sugar release in transgenic grasses and display altered cytokinin homeostasis. PLoS Genet. 13, e1006649 (2017).

[9]

Voorend, W. et al. Overexpression of GA20-OXIDASE1 impacts plant height, biomass allocation and saccharification efficiency in maize. Plant Biotechnol. J. 14, 997-1007 (2016).

[10]

Santner, A., Calderon-Villalobos, L. I. & Estelle, M. Plant hormones are versatile chemical regulators of plant growth. Nat. Chem. Biol. 5, 301-307 (2009).

[11]

Yamaguchi, S. Gibberellin metabolism and its regulation. Annu. Rev. Plant Biol. 59, 225-251 (2008).

[12]

Miao, C., Wang, D., He, R., Liu, S. & Zhu, J. K. Mutations in MIR396e and MIR396f increase grain size and modulate shoot architecture in rice. Plant Biotechnol. J. 18, 491-501 (2020).

[13]

Hu, S. et al. Xiaowei, a new rice germplasm for large-scale indoor research. Mol. Plant 11, 1418-1420 (2018).

[14]

Cheng, J. et al. A single nucleotide mutation in GID1c disrupts its interaction with DELLA1 and causes a GA-insensitive dwarf phenotype in peach. Plant Biotechnol. J. 17, 1723-1735 (2019).

[15]

Dayan, J., Schwarzkopf, M., Avni, A. & Aloni, R. Enhancing plant growth and fiber production by silencing GA-oxidase. Plant Biotechnol. J. 8, 425-435 (2010).

[16]

Yan, J. et al. Ectopic expression of GA 2-oxidase 6 from rapeseed (Brassica napus L.) causes dwarfism, late flowering and enhanced chlorophyll accumulation in Arabidopsis thaliana. Plant Physiol. Biochem. 111, 10-19 (2017).

[17]

Haecker, A. et al. Expression dynamics of WOX genes mark cell fate decisions during early embryonic patterning in Arabidopsis thaliana. Development 131, 657-668 (2004).

[18]

Somssich, M., Je, B. I., Simon, R. & Jackson, D. CLAVATA-WUSCHEL signaling in the shoot meristem. Development 143, 3238-3324 (2016).

[19]

Nakata, M. et al. Roles of the middle domain-specific WUSCHEL-RELATED HOMEOBOX genes in early development of leaves in Arabidopsis. Plant Cell 24, 519-535 (2012).

[20]

Ishiwata, A. et al. Two WUSCHEL-related homeobox genes, narrow leaf2 and narrow leaf3, control leaf width in rice. Plant Cell Physiol. 54, 779-792 (2013).

[21]

Nardmann, J., Ji, J., Werr, W. & Scanlon, M. J. The maize duplicate genes narrow sheath1 and narrow sheath2 encode a conserved homeobox gene function in a lateral domain of shoot apical meristems. Development 131, 2827-2839 (2004).

[22]

Cho, S. H., Kang, K., Lee, S. H., Lee, I. J. & Paek, N. C. OsWOX3A is involved in negative feedback regulation of the gibberellic acid biosynthetic pathway in rice (Oryza sativa). J. Exp. Bot. 67, 1677-1687 (2016).

[23]

Cho, S. H. et al. The rice narrow leaf2 and narrow leaf3 loci encode WUSCHEL-related homeobox 3A (OsWOX3A) and function in leaf, spikelet, tiller and lateral root development. New Phytol. 198, 1071-1084 (2013).

[24]

Wang, H. et al. WUSCHEL-related homeobox1 (WOX1) regulates vein patterning and leaf size in Cucumis sativus. Hortic. Res. 7, 182 (2020).

[25]

Tadege, M. et al. STENOFOLIA regulates blade outgrowth and leaf vascular patterning in Medicago truncatula and Nicotiana sylvestris. Plant Cell 23, 2125-2142 (2011).

[26]

Fu, C. et al. Overexpression of miR156 in switchgrass (Panicum virgatum L.) results in various morphological alterations and leads to improved biomass production. Plant Biotechnol. J. 210, 443-452 (2012).

[27]

Hardin, C. F. et al. Standardization of switchgrass sample collection for cell wall and biomass trait analysis. Bioenergy Res. 6, 755-762 (2013).

[28]

Li, X. et al. Identification and evolution of the WUSCHEL-related homeobox protein family in Bambusoideae. Biomolecules 10, 739 (2020).

[29]

Meng, Y. et al. HEADLESS, a WUSCHEL homolog, uncovers novel aspects of shoot meristem regulation and leaf blade development in Medicago truncatula. J. Exp. Bot. 70, 149-163 (2019).

[30]

Marchler-Bauer, A. et al. CDD/SPARCLE: functional classification of proteins via subfamily domain architectures. Nucleic Acids Res. 45, D200-D203 (2017).

[31]

Kumar, S., Stecher, G., Li, M., Knyaz, C. & Tamura, K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol. Biol. Evol. 35, 1547-1549 (2018).

[32]

Zhao, H., Tan, Z., Wen, X. & Wang, Y. An improved syringe agroinfiltration protocol to enhance transformation efficiency by combinative use of 5-azacytidine, ascorbate acid and Tween-20. Plants 6, E9 (2017).

[33]

Mann, D. G. et al. Gateway-compatible vectors for high-throughput gene functional analysis in switchgrass (Panicum virgatum L.) and other monocot species. Plant Biotechnol. J. 10, 226-236 (2012).

[34]

Curtis, M. D. & Grossniklaus, U. A gateway cloning vector set for high-throughput functional analysis of genes in planta. Plant Physiol. 133, 462-469 (2003).

[35]

Xi, Y. et al. Agrobacterium-mediated transformation of switchgrass and inheritance of the transgenes. Bioenergy Res. 2, 275-283 (2009).

[36]

Hellens, R. P. et al. Transient expression vectors for functional genomics, quantification of promoter activity and RNA silencing in plants. Plant Methods 1, 13 (2005).

[37]

Chen, F. & Dixon, R. A. Lignin modification improves fermentable sugar yields for biofuel production. Nat. Biotechnol. 25, 759-761 (2007).

[38]

Jung, H., Varel, V. H., Weimer, P. J. & Ralph, J. Accuracy of Klason lignin and acid detergent lignin methods as assessed by bomb calorimetry. J. Agric. Food Chem. 47, 2005-2008 (1999).

[39]

Peng, X. et al. Characterization of hemicellulose and cellulase from the extremely thermophilic bacterium Caldicellulosiruptor owensensis and their potential application for bioconversion of lignocellulosic biomass without pretreatment. Biotechnol. Biofuels 8, 131 (2015).

[40]

Dubois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A. & Smith, F. Colorimetric method for determination of sugars and related substances. Anal. Chem. 28, 350-356 (1956).

[41]

Van der Graaff, E., Laux, T. & Rensing, S. A. The WUS homeobox-containing (WOX) protein family. Genome Biol. 10, 248 (2009).

[42]

Shimizu, R. et al. Tissue specificity and evolution of meristematic WOX3 function. Plant Physiol. 149, 841-850 (2009).

[43]

Do, P. T. et al. Expression of ZmGA20ox cDNA alters plant morphology and increases biomass production of switchgrass (Panicum virgatum L.). Plant Biotechnol. J. 14, 1532-1540 (2016).

[44]

Falcioni, R. et al. Increased gibberellins and light levels promotes cell wall thickness and enhance lignin deposition in xylem fibers. Front. Plant Sci. 9, 1391 (2018).

[45]

Chuck, G., Cigan, A. M., Saeteurn, K. & Hake, S. The heterochronic maize mutant Corngrass1 results from overexpression of a tandem microRNA. Nat. Genet. 39, 544-549 (2007).

[46]

Mao, Y. B. et al. Jasmonate response decay and defense metabolite accumulation contributes to age regulated dynamics of plant insect resistance. Nat. Commun. 8, 13925 (2017).

[47]

Song, X. et al. IPA1 functions as a downstream transcription factor repressed by D53 in strigolactone signaling in rice. Cell Res. 27, 1128-1141 (2017).

[48]

Ye, B. B. et al. AP2/ERF transcription factors integrate age and wound signals for root regeneration. Plant Cell 32, 226-241 (2020).

[49]

Zhang, T. Q. et al. An intrinsic microRNA timer regulates progressive decline in shoot regenerative capacity in plants. Plant Cell 27, 349-360 (2015).

[50]

Hyun, Y. et al. Multi-layered regulation of SPL15 and cooperation with SOC1 integrate endogenous flowering pathways at the Arabidopsis shoot meristem. Dev. Cell 37, 254-266 (2016).

[51]

Galvao, V. C., Horrer, D., Kuttner, F. & Schmid, M. Spatial control of flowering by DELLA proteins in Arabidopsis thaliana. Development 139, 4072-4082 (2012).

[52]

Chuck, G. S. et al. Overexpression of the maize Corngrass1 microRNA prevents flowering, improves digestibility, and increases starch content of switchgrass. Proc. Natl Acad. Sci. USA 108, 17550-17555 (2011).

PDF (1672KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/