The role of γ-aminobutyric acid in aluminum stress tolerance in a woody plant, Liriodendron chinense × tulipifera

Pengkai Wang , Yini Dong , Liming Zhu , Zhaodong Hao , LingFeng Hu , Xiangyang Hu , Guibin Wang , Tielong Cheng , Jisen Shi , Jinhui Chen

Horticulture Research ›› 2021, Vol. 8 ›› Issue (1) : 80

PDF (2035KB)
Horticulture Research ›› 2021, Vol. 8 ›› Issue (1) :80 DOI: 10.1038/s41438-021-00517-y
Article
research-article
The role of γ-aminobutyric acid in aluminum stress tolerance in a woody plant, Liriodendron chinense × tulipifera
Author information +
History +
PDF (2035KB)

Abstract

The aluminum (Al) cation Al3+ in acidic soil shows severe rhizotoxicity that inhibits plant growth and development. Most woody plants adapted to acidic soils have evolved specific strategies against Al3+ toxicity, but the underlying mechanism remains elusive. The four-carbon amino acid gamma-aminobutyric acid (GABA) has been well studied in mammals as an inhibitory neurotransmitter; GABA also controls many physiological responses during environmental or biotic stress. The woody plant hybrid Liriodendron (L. chinense × tulipifera) is widely cultivated in China as a horticultural tree and provides high-quality timber; studying its adaptation to high Al stress is important for harnessing its ecological and economic potential. Here, we performed quantitative iTRAQ (isobaric tags for relative and absolute quantification) to study how protein expression is altered in hybrid Liriodendron leaves subjected to Al stress. Hybrid Liriodendron shows differential accumulation of several proteins related to cell wall biosynthesis, sugar and proline metabolism, antioxidant activity, cell autophagy, protein ubiquitination degradation, and anion transport in response to Al damage. We observed that Al stress upregulated glutamate decarboxylase (GAD) and its activity, leading to increased GABA biosynthesis. Additional GABA synergistically increased Al-induced antioxidant enzyme activity to efficiently scavenge ROS, enhanced proline biosynthesis, and upregulated the expression of MATE1/2, which subsequently promoted the efflux of citrate for chelation of Al3+. We also showed similar effects of GABA on enhanced Al3+ tolerance in Arabidopsis. Thus, our findings suggest a function of GABA signaling in enhancing hybrid Liriodendron tolerance to Al stress through promoting organic acid transport and sustaining the cellular redox and osmotic balance.

Cite this article

Download citation ▾
Pengkai Wang, Yini Dong, Liming Zhu, Zhaodong Hao, LingFeng Hu, Xiangyang Hu, Guibin Wang, Tielong Cheng, Jisen Shi, Jinhui Chen. The role of γ-aminobutyric acid in aluminum stress tolerance in a woody plant, Liriodendron chinense × tulipifera. Horticulture Research, 2021, 8 (1) : 80 DOI:10.1038/s41438-021-00517-y

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Kochian, L. V., Pineros, M. A. & Hoekenga, O. A. The physiology, genetics and molecular biology of plant aluminum resistance and toxicity. Plant Soil 274, 175-195 (2005).

[2]

Horst, W. J., Wang, Y. & Eticha, D. The role of the root apoplast in aluminium-induced inhibition of root elongation and in aluminium resistance of plants: a review. Ann. Bot. 106, 185-197 (2010).

[3]

Sade, H. et al. Toxicity and tolerance of aluminum in plants: tailoring plants to suit to acid soils. Biometals 29, 187-210 (2016).

[4]

Kochian, L. V., Pineros, M. A., Liu, J. & Magalhaes, J. V. Plant adaptation to acid soils: the molecular basis for crop aluminum resistance. Annu. Rev. Plant Biol. 66, 571-598 (2015).

[5]

Uexküll, H. R. V. & Mutert, E. Global extent, development and economic impact of acid soils. Plant Soil 171, 1-15 (1995).

[6]

Matsumoto, H. Cell biology of aluminum toxicity and tolerance in higher plants. Int. Rev. Cytol. 200, 1-46 (2000).

[7]

Ahonen-Jonnarth, U., Goransson, A. & Finlay, R. D. Growth and nutrient uptake of ectomycorrhizal Pinus sylvestris seedlings in a natural substrate treated with elevated Al concentrations. Tree Physiol. 23, 157-167 (2003).

[8]

Grisel, N. et al. Transcriptome responses to aluminum stress in roots of aspen (Populus tremula). Bmc Plant Biol. 10, 185 https://doi.org/10.1186/1471-2229-10-185 (2010).

[9]

Sasaki, T. et al. A wheat gene encoding an aluminum-activated malate transporter. Plant J.: Cell Mol. Biol. 37, 645-653 (2004).

[10]

Hoekenga, O. A. et al. AtALMT1, which encodes a malate transporter, is identified as one of several genes critical for aluminum tolerance in Arabidopsis. Proc. Natl Acad. Sci. USA 103, 9738-9743 (2006).

[11]

Ligaba, A., Katsuhara, M., Ryan, P. R., Shibasaka, M. & Matsumoto, H. The BnALMT1 and BnALMT2 genes from rape encode aluminum-activated malate transporters that enhance the aluminum resistance of plant cells. Plant Physiol. 142, 1294-1303 (2006).

[12]

Magalhaes, J. V. et al. A gene in the multidrug and toxic compound extrusion (MATE) family confers aluminum tolerance in sorghum. Nat. Genet. 39, 1156-1161 (2007).

[13]

Upadhyay, N. et al. The multitasking abilities of MATE transporters in plants. J. Exp. Botany, https://doi.org/10.1093/jxb/erz246 (2019).

[14]

Iuchi, S. et al. Zinc finger protein STOP1 is critical for proton tolerance in Arabidopsis and coregulates a key gene in aluminum tolerance. Proc. Natl Acad. Sci. USA 104, 9900-9905 (2007).

[15]

Tsutsui, T., Yamaji, N. & Feng Ma, J. Identification of a cis-acting element of ART1, a C2H2-type zinc-finger transcription factor for aluminum tolerance in rice. Plant Physiol. 156, 925-931 (2011).

[16]

Ding, Z. J., Yan, J. Y., Xu, X. Y., Li, G. X. & Zheng, S. J. WRKY46 functions as a transcriptional repressor of ALMT1, regulating aluminum-induced malate secretion in Arabidopsis. Plant J. 76, 825-835 (2013).

[17]

Wang, J. P., Raman, H., Zhang, G. P., Mendham, N. & Zhou, M. X. Aluminium tolerance in barley (Hordeum vulgare L.): physiological mechanisms, genetics and screening methods. J. Zhejiang Univ. Sci. B 7, 769-787 (2006).

[18]

Taylor, G. J. et al. Direct measurement of aluminum uptake and distribution in single cells of Chara corallina. Plant Physiol. 123, 987-996 (2000).

[19]

Shelp, B. J., Bown, A. W. & McLean, M. D. Metabolism and functions of gamma-aminobutyric acid. Trends Plant Sci. 4, 446-452 (1999).

[20]

Kinnersley, A. M. & Turano, F. J. Gamma aminobutyric acid (GABA) and plant responses to stress. Crit. Rev. Plant Sci. 19, 479-509 (2000).

[21]

Bouche, N. & Fromm, H. GABA in plants: just a metabolite? Trends Plant Sci. 9, 110-115 (2004).

[22]

Renault, H. et al. The Arabidopsis pop2-1 mutant reveals the involvement of GABA transaminase in salt stress tolerance. Bmc Plant Biol. 10, 20 (2010).

[23]

Ramesh, S. A. et al. GABA signalling modulates plant growth by directly regulating the activity of plant-specific anion transporters. Nat. Commun. 6, 7879 (2015).

[24]

Ramesh, S. A. et al. Aluminum-activated malate transporters can facilitate GABA transport([OPEN]). Plant Cell 30, 1147-1164 (2018).

[25]

Chen, J. et al. Liriodendron genome sheds light on angiosperm phylogeny and species-pair differentiation. Nat. Plants 5, 18-25 (2019).

[26]

Huo, A. et al. Establishment of transient gene expression systems in protoplasts from Liriodendron hybrid mesophyll cells. PLoS ONE 12, e0172475 (2017).

[27]

Bai, X. G. et al. Deciphering the protective role of nitric oxide against salt stress at the physiological and proteomic levels in maize. J. Proteome Res. 10, 4349-4364 (2011).

[28]

Hu, X. Y., Neill, S. J., Cai, W. M. & Tang, Z. C. Induction of defence gene expression by oligogalacturonic acid requires increases in both cytosolic calcium and hydrogen peroxide in Arabidopsis thaliana. Cell Res. 14, 234-240 (2004).

[29]

Elstner, E. F. & Heupel, A. Inhibition of nitrite formation from hydroxylammoniumchloride: a simple assay for superoxide dismutase. Anal. Biochem. 70, 616-620 (1976).

[30]

Zhang, G. J. & Bown, A. W. The rapid determination of gamma-aminobutyric acid. Phytochemistry 44, 1007-1009 (1997).

[31]

Cheng, T. L. et al. Quantitative proteomics analysis reveals that S-nitrosoglutathione reductase (GSNOR) and nitric oxide signaling enhance poplar defense against chilling stress. Planta 242, 1361-1390 (2015).

[32]

Bouche, N., Fait, A., Bouchez, D., Moller, S. G. & Fromm, H. Mitochondrial succinic-semialdehyde dehydrogenase of the gamma-aminobutyrate shunt is required to restrict levels of reactive oxygen intermediates in plants. Proc. Natl Acad. Sci. USA 100, 6843-6848 (2003).

[33]

Szabados, L. & Savoure, A. Proline: a multifunctional amino acid. Trends Plant Sci. 15, 89-97 (2010).

[34]

Verslues, P. E. & Sharma, S. Proline metabolism and its implications for plant-environment interaction. Arabidopsis Book 8, e0140 (2010).

[35]

Liu, J., Magalhaes, J. V., Shaff, J. & Kochian, L. V. Aluminum-activated citrate and malate transporters from the MATE and ALMT families function independently to confer Arabidopsis aluminum tolerance. Plant J.: cell Mol. Biol. 57, 389-399 (2009).

[36]

Zimmerli, L., Jakab, G., Métraux, J.-P. & Mauch-Mani, B. Potentiation of pathogen-specific defense mechanisms in Arabidopsis by β-aminobutyric acid. Proc. Natl Acad. Sci. 97, 12920 (2000).

[37]

Cohen, Y. The BABA story of induced resistance. Phytoparasitica 29, 375 (2001).

[38]

Seifikalhor, M., Aliniaeifard, S., Hassani, B., Niknam, V. & Lastochkina, O. Diverse role of γ-aminobutyric acid in dynamic plant cell responses. Plant Cell Rep. 38, 847-867 (2019).

[39]

Ramesh, S. A., Tyerman, S. D., Gilliham, M. & Xu, B. γ-Aminobutyric acid (GABA) signalling in plants. Cell. Mol. Life Sci. 74, 1577-1603 (2017).

[40]

Shelp, B. J., Bown, A. W. & Faure, D. Extracellular γ-aminobutyrate mediates communication between plants and other organisms. Plant Physiol. 142, 1350 (2006).

[41]

Geng, X. et al. LEUNIG_HOMOLOG transcriptional co-repressor mediates aluminium sensitivity through PECTIN METHYLESTERASE46-modulated root cell wall pectin methylesterification in Arabidopsis. Plant J.: Cell Mol. Biol. 90, 491-504 (2017).

[42]

Zhang, Y. et al. F-box protein RAE1 regulates the stability of the aluminum-resistance transcription factor STOP1 in Arabidopsis. Proc. Natl Acad. Sci. USA 116, 319-327 (2019).

[43]

Khan, N., Bano, A., Rahman, M. A., Rathinasabapathi, B. & Babar, M. A. UPLC-HRMS-based untargeted metabolic profiling reveals changes in chickpea (Cicer arietinum) metabolome following long-term drought stress. Plant, Cell Environ. 42, 115-132 (2019).

[44]

Bose, J., Rodrigo-Moreno, A. & Shabala, S. ROS homeostasis in halophytes in the context of salinity stress tolerance. J. Exp. Bot. 65, 1241-1257 (2014).

PDF (2035KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/