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Autotoxicity Mechanism of Oryza Sativa: Transcriptome Response in Rice Roots Exposed to Ferulic Acid

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2013 May 28
PMID 23705659
Citations 21
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Abstract

Background: Autotoxicity plays an important role in regulating crop yield and quality. To help characterize the autotoxicity mechanism of rice, we performed a large-scale, transcriptomic analysis of the rice root response to ferulic acid, an autotoxin from rice straw.

Results: Root growth rate was decreased and reactive oxygen species, calcium content and lipoxygenase activity were increased with increasing ferulic acid concentration in roots. Transcriptome analysis revealed more transcripts responsive to short ferulic-acid exposure (1- and 3-h treatments, 1,204 genes) than long exposure (24 h, 176 genes). Induced genes were involved in cell wall formation, chemical detoxification, secondary metabolism, signal transduction, and abiotic stress response. Genes associated with signaling and biosynthesis for ethylene and jasmonic acid were upregulated with ferulic acid. Ferulic acid upregulated ATP-binding cassette and amino acid/auxin permease transporters as well as genes encoding signaling components such as leucine-rich repeat VIII and receptor-like cytoplasmic kinases VII protein kinases, APETALA2/ethylene response factor, WRKY, MYB and Zinc-finger protein expressed in inflorescence meristem transcription factors.

Conclusions: The results of a transcriptome analysis suggest the molecular mechanisms of plants in response to FA, including toxicity, detoxicification and signaling machinery. FA may have a significant effect on inhibiting rice root elongation through modulating ET and JA hormone homeostasis. FA-induced gene expression of AAAP transporters may contribute to detoxicification of the autotoxin. Moreover, the WRKY and Myb TFs and LRR-VIII and SD-2b kinases might regulate downstream genes under FA stress but not general allelochemical stress. This comprehensive description of gene expression information could greatly facilitate our understanding of the mechanisms of autotoxicity in plants.

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References
1.
Shin R, Park J, An J, Paek K . Ectopic expression of Tsi1 in transgenic hot pepper plants enhances host resistance to viral, bacterial, and oomycete pathogens. Mol Plant Microbe Interact. 2002; 15(10):983-9. DOI: 10.1094/MPMI.2002.15.10.983. View

2.
Baziramakenga R, Leroux G, Simard R . Effects of benzoic and cinnamic acids on membrane permeability of soybean roots. J Chem Ecol. 2013; 21(9):1271-85. DOI: 10.1007/BF02027561. View

3.
Wang H, Hao J, Chen X, Hao Z, Wang X, Lou Y . Overexpression of rice WRKY89 enhances ultraviolet B tolerance and disease resistance in rice plants. Plant Mol Biol. 2007; 65(6):799-815. DOI: 10.1007/s11103-007-9244-x. View

4.
Sanchez M, Pena M, Revilla G, Zarra I . Changes in Dehydrodiferulic Acids and Peroxidase Activity against Ferulic Acid Associated with Cell Walls during Growth of Pinus pinaster Hypocotyl. Plant Physiol. 1996; 111(3):941-946. PMC: 157913. DOI: 10.1104/pp.111.3.941. View

5.
Huang T, Huang H . ROS and CDPK-like kinase-mediated activation of MAP kinase in rice roots exposed to lead. Chemosphere. 2008; 71(7):1377-85. DOI: 10.1016/j.chemosphere.2007.11.031. View