Transcriptome-wide effect of Salix SmSPR1 in etiolated seedling of Arabidopsis

Xiaoxia Liu , Jianguo Zhang , Li Xue , Guodong Rao

Journal of Forestry Research ›› 2020, Vol. 32 ›› Issue (3) : 975 -985.

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Journal of Forestry Research ›› 2020, Vol. 32 ›› Issue (3) : 975 -985. DOI: 10.1007/s11676-020-01202-x
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Transcriptome-wide effect of Salix SmSPR1 in etiolated seedling of Arabidopsis

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Abstract

Microtubules and their regulatory proteins are involved in the regulation of plant cell morphology. SPIRAL1 (SPR1), a plant-specific microtubule-binding protein, is critical in regulating the anisotropic growth of plant cells. Our previous study showed that overexpressed Salix SmSPR1 genes in Arabidopsis thaliana caused right-handed spiral elongation in etiolated seedlings, but there were no morphological differences between wild-type and transgenic seedlings under varied light conditions. We then studied the transcriptional regulation patterns in transgenic plants engineered with the SmSPR1 gene. Transcriptomic results showed that a large number of differentially expressed genes were involved in plant light signal reception, chlorophyll synthesis and photosystem structure. Eleven gene families with 42 photosynthesis-related genes and 6 light-responsive genes were involved in regulation of cell morphology. Our results showed that these genes in the SmSPR1-ox line were particularly down-regulated under dark conditions. In addition, 33 TFs showed differences between SmSPR1-ox and wild-type lines. Taken together, the transcriptome analysis provides new insight into investigating the molecular mechanisms of light-induced cell morphological changes mediated by the microtubule binding protein SPR1.

Keywords

Arabidopsis thaliana / Cell anisotropism / SmSPR1 / Transcription factor / Transcriptome analysis

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Xiaoxia Liu, Jianguo Zhang, Li Xue, Guodong Rao. Transcriptome-wide effect of Salix SmSPR1 in etiolated seedling of Arabidopsis. Journal of Forestry Research, 2020, 32(3): 975-985 DOI:10.1007/s11676-020-01202-x

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References

[1]

Alabadi D, Blazquez MA, Carbonell J, Ferrandiz C, Perez-Amador MA. Instructive roles for hormones in plant development. Int J Dev Biol, 2009, 53(8–10): 1597-1608.

[2]

Alabadi D, Gil J, Blazquez MA, Garcia-Martinez JL. Gibberellins repress photomorphogenesis in darkness. Plant Physiol, 2004, 134(3): 1050-1057.

[3]

Aldridge C, Maple J, Moller SG. The molecular biology of plastid division in higher plants. J Exp Bot, 2005, 56(414): 1061-1077.

[4]

Balcerowicz M, Kerner K, Schenkel C, Hoecker U. SPA proteins affect the subcellular localization of COP1 in the COP1/SPA ubiquitin ligase complex during photomorphogenesis. Plant Physiol, 2017, 174(3): 1314-1321.

[5]

Bisgrove SR, Lee YR, Liu B, Peters NT, Kropf DL. The microtubule plus-end binding protein EB1 functions in root responses to touch and gravity signals in Arabidopsis. Plant Cell, 2008, 20(2): 396-410.

[6]

Chen S, Lory N, Stauber J, Hoecker U. Photoreceptor specificity in the light-induced and COP1-mediated rapid degradation of the repressor of rhotomorphogenesis SPA2 in Arabidopsis. PLoS Genet, 2015 11 9 e1005516

[7]

Ericson ML, Rodin J, Lenman M, Glimelius K, Josefsson LG, Rask L. Structure of the rapeseed 1.7 S storage protein, napin, and its precursor. J Biol Chem, 1986, 261(31): 14576-14581.

[8]

Friso G, Giacomelli L, Ytterberg AJ, Peltier JB, Rudella A, Sun Q, Wijk KJ. In-depth analysis of the thylakoid membrane proteome of Arabidopsis thaliana chloroplasts: new proteins, new functions, and a plastid proteome database. Plant Cell, 2004, 16(2): 478-499.

[9]

Furutani I, Watanabe Y, Prieto R, Masukawa M, Hashimoto T. The SPIRAL genes are required for directional control of cell elongation in Arabidopsis thaliana. Development, 2000, 127(20): 4443-4453.

[10]

Galva C, Kirik V, Lindeboom JJ, Kaloriti D, Rancour DM, Hussey PJ, Bednarek SY, Ehrhardt DW, Sedbrook JC. The microtubule plus-end tracking proteins SPR1 and EB1b interact to maintain polar cell elongation and directional organ growth in Arabidopsis. Plant Cell, 2014, 26(11): 4409-4425.

[11]

Gangappa SN, Botto JF. The BBX family of plant transcription factors. Trends Plant Sci, 2014, 19(7): 460-470.

[12]

Gangappa SN, Botto JF. The multifaceted roles of HY5 in plant growth and development. Mol Plant, 2016, 9(10): 1353-1365.

[13]

Gang HY, Li RH, Zhao YM, Liu GF, Chen S, Jiang J. Loss of GLK1 transcription factor function reveals new insights in chlorophyll biosynthesis and chloroplast development. J Exp Bot, 2019, 70(12): 3125-3138.

[14]

Gardiner J. The evolution and diversification of plant microtubule-associated proteins. Plant J, 2013, 75(2): 219-229.

[15]

Gardiner J, Overall R, Marc J. Plant microtubule cytoskeleton complexity: microtubule arrays as fractals. J Exp Bot, 2011, 63(2): 635-642.

[16]

Hashimoto T. Microtubules in plants. Arabidopsis book, 2015, Rockville: American Society of Plant Biologists e0179

[17]

Jiang X, Li H, Wang T, Peng C, Wang H, Wu H, Wang X. Gibberellin indirectly promotes chloroplast biogenesis as a means to maintain the chloroplast population of expanded cells. Plant J, 2012, 72(5): 768-780.

[18]

Ling JJ, Li J, Zhu D, Deng XW. Noncanonical role of Arabidopsis COP1/SPA complex in repressing BIN2-mediated PIF3 phosphorylation and degradation in darkness. Proc Natl Acad Sci U S A, 2017, 114(13): 3539-3544.

[19]

Liu X, Qin T, Ma Q, Sun J, Liu Z, Yuan M, Mao T. Light-regulated hypocotyl elongation involves proteasome-dependent degradation of the microtubule regulatory protein WDL3 in Arabidopsis. Plant Cell, 2013, 25(5): 1740-1755.

[20]

Liu X, Zhang J, Sui J, Luo Y, Rao G. The Salix SmSPR1 involved in light-regulated cell expansion by modulating microtubule arrangement. Front Cell Dev Biol, 2019, 7: 309.

[21]

Luo XM, Lin WH, Zhu S, Zhu JY, Sun Y, Fan XY, Cheng M. Integration of light- and brassinosteroid-signaling pathways by a GATA transcription factor in Arabidopsis. Dev Cell, 2010, 19(6): 872-883.

[22]

Ma Q, Wang X, Sun J, Mao T. Coordinated regulation of hypocotyl cell elongation by light and ethylene through a microtubule destabilizing protein. Plant Physiol, 2018 176 1 678

[23]

Nakajima K, Furutani I, Tachimoto H, Matsubara H, Hashimoto T. SPIRAL1 encodes a plant-specific microtubule-localized protein required for directional control of rapidly expanding Arabidopsis cells. Plant Cell, 2004, 16(5): 1178-1190.

[24]

Nakajima K, Kawamura T, Hashimoto T. Role of the SPIRAL1 gene family in anisotropic growth of Arabidopsis thaliana. Plant Cell Physiol, 2006, 47(4): 513-522.

[25]

Okazaki K, Kabeya Y, Miyagishima SY. The evolution of the regulatory mechanism of chloroplast division. Plant Signal Behav, 2010, 5(2): 164-167.

[26]

Paddock TN, Mason ME, Lima DF, Armstrong GA. Arabidopsis protochlorophyllide oxidoreductase A (PORA) restores bulk chlorophyll synthesis and normal development to aporB porCdouble mutant. Plant Mol Biol, 2010, 72(4–5): 445-457.

[27]

Saijo Y, Sullivan JA, Wang H, Yang J, Shen Y, Rubio V, Ma L, Hoecker U, Deng XW. The COP1-SPA1 interaction defines a critical step in phytochrome A-mediated regulation of HY5 activity. Genes Dev, 2003, 17(21): 2642-2647.

[28]

Sedbrook JC, Ehrhardt DW, Fisher SE, Scheible WR, Somerville CR. The Arabidopsis sku6/spiral1 gene encodes a plus end-localized microtubule-interacting protein involved in directional cell expansion. Plant Cell, 2004, 16(6): 1506-1520.

[29]

Seo HS, Watanabe E, Tokutomi S, Nagatani A, Chua NH. Photoreceptor ubiquitination by COP1 E3 ligase desensitizes phytochrome A signaling. Genes Dev, 2004, 18(6): 617-622.

[30]

Srivastava AK, Senapati D, Srivastava A, Chakraborty M, Gangappa SN, Chattopadhyay S. Short hypocotyl in white light1 interacts with elongated hypocotyl5 (HY5) and constitutive photomorphogenic1 (COP1) and promotes COP1-mediated degradation of HY5 during Arabidopsis seedling development. Plant Physiol, 2015, 169(4): 2922-2934.

[31]

Xu X, Chi W, Sun X, Feng P, Guo H, Li J, Lin R. Convergence of light and chloroplast signals for de-etiolation through ABI4-HY5 and COP1. Nat Plants, 2016 2 6 16066

[32]

Zhang X, Huai J, Shang F, Xu G, Tang W, Jing Y, Lin R. A PIF1/PIF3-HY5-BBX23 transcription factor cascade affects photomorphogenesis. Plant Physiol, 2017, 174(4): 2487-2500.

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