A Group VII Ethylene Response Factor Gene, ZmEREB180, Coordinates Waterlogging Tolerance in Maize Seedlings

Overview

Journal Plant Biotechnol J

Specialties Biology
Biotechnology

Date 2019 Apr 30

PMID 31033158

Citations 48

Authors

Feng Yu

Kun Liang

Tian Fang

Hailiang Zhao

Xuesong Han

Manjun Cai

Fazhan Qiu

Affiliations

Soon will be listed here.

Abstract

Group VII ethylene response factors (ERFVIIs) play important roles in ethylene signalling and plant responses to flooding. However, natural ERFVII variations in maize (ZmERFVIIs) that are directly associated with waterlogging tolerance have not been reported. Here, a candidate gene association analysis of the ZmERFVII gene family showed that a waterlogging-responsive gene, ZmEREB180, was tightly associated with waterlogging tolerance. ZmEREB180 expression specifically responded to waterlogging and was up-regulated by ethylene; in addition, its gene product localized to the nucleus. Variations in the 5'-untranslated region (5'-UTR) and mRNA abundance of this gene under waterlogging conditions were significantly associated with survival rate (SR). Ectopic expression of ZmEREB180 in Arabidopsis increased the SR after submergence stress, and overexpression of ZmEREB180 in maize also enhanced the SR after long-term waterlogging stress, apparently through enhanced formation of adventitious roots (ARs) and regulation of antioxidant levels. Transcriptomic assays of the transgenic maize line under normal and waterlogged conditions further provided evidence that ZmEREB180 regulated AR development and reactive oxygen species homeostasis. Our study provides direct evidence that a ZmERFVII gene is involved in waterlogging tolerance. These findings could be applied directly to breed waterlogging-tolerant maize cultivars and improve our understanding of waterlogging stress.

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References

Bailey-Serres J, Voesenek L . Flooding stress: acclimations and genetic diversity. Annu Rev Plant Biol. 2008; 59:313-39. DOI: 10.1146/annurev.arplant.59.032607.092752. View

Nanjo Y, Maruyama K, Yasue H, Yamaguchi-Shinozaki K, Shinozaki K, Komatsu S . Transcriptional responses to flooding stress in roots including hypocotyl of soybean seedlings. Plant Mol Biol. 2011; 77(1-2):129-44. DOI: 10.1007/s11103-011-9799-4. View

Osman K, Tang B, Wang Y, Chen J, Yu F, Li L . Dynamic QTL analysis and candidate gene mapping for waterlogging tolerance at maize seedling stage. PLoS One. 2013; 8(11):e79305. PMC: 3828346. DOI: 10.1371/journal.pone.0079305. View

Voesenek L, Bailey-Serres J . Flood adaptive traits and processes: an overview. New Phytol. 2015; 206(1):57-73. DOI: 10.1111/nph.13209. View

Argus R, Colmer T, Grierson P . Early physiological flood tolerance is followed by slow post-flooding root recovery in the dryland riparian tree Eucalyptus camaldulensis subsp. refulgens. Plant Cell Environ. 2014; 38(6):1189-99. DOI: 10.1111/pce.12473. View

Shabala S . Physiological and cellular aspects of phytotoxicity tolerance in plants: the role of membrane transporters and implications for crop breeding for waterlogging tolerance. New Phytol. 2011; 190(2):289-98. DOI: 10.1111/j.1469-8137.2010.03575.x. View

Abiko T, Kotula L, Shiono K, Malik A, Colmer T, Nakazono M . Enhanced formation of aerenchyma and induction of a barrier to radial oxygen loss in adventitious roots of Zea nicaraguensis contribute to its waterlogging tolerance as compared with maize (Zea mays ssp. mays). Plant Cell Environ. 2012; 35(9):1618-30. DOI: 10.1111/j.1365-3040.2012.02513.x. View

Licausi F, Kosmacz M, Weits D, Giuntoli B, Giorgi F, Voesenek L . Oxygen sensing in plants is mediated by an N-end rule pathway for protein destabilization. Nature. 2011; 479(7373):419-22. DOI: 10.1038/nature10536. View

van Loon L, Geraats B, Linthorst H . Ethylene as a modulator of disease resistance in plants. Trends Plant Sci. 2006; 11(4):184-91. DOI: 10.1016/j.tplants.2006.02.005. View

10.

Steffens B . The role of ethylene and ROS in salinity, heavy metal, and flooding responses in rice. Front Plant Sci. 2014; 5:685. PMC: 4255495. DOI: 10.3389/fpls.2014.00685. View

11.

Raskin I, Kende H . Role of gibberellin in the growth response of submerged deep water rice. Plant Physiol. 1984; 76(4):947-50. PMC: 1064412. DOI: 10.1104/pp.76.4.947. View

12.

Jiao Y, Peluso P, Shi J, Liang T, Stitzer M, Wang B . Improved maize reference genome with single-molecule technologies. Nature. 2017; 546(7659):524-527. PMC: 7052699. DOI: 10.1038/nature22971. View

13.

Fukao T, Bailey-Serres J . Plant responses to hypoxia--is survival a balancing act?. Trends Plant Sci. 2004; 9(9):449-56. DOI: 10.1016/j.tplants.2004.07.005. View

14.

Mustroph A, Lee S, Oosumi T, Zanetti M, Yang H, Ma K . Cross-kingdom comparison of transcriptomic adjustments to low-oxygen stress highlights conserved and plant-specific responses. Plant Physiol. 2010; 152(3):1484-500. PMC: 2832244. DOI: 10.1104/pp.109.151845. View

15.

Kurokawa Y, Nagai K, Huan P, Shimazaki K, Qu H, Mori Y . Rice leaf hydrophobicity and gas films are conferred by a wax synthesis gene (LGF1) and contribute to flood tolerance. New Phytol. 2018; 218(4):1558-1569. DOI: 10.1111/nph.15070. View

16.

Hinz M, Wilson I, Yang J, Buerstenbinder K, Llewellyn D, Dennis E . Arabidopsis RAP2.2: an ethylene response transcription factor that is important for hypoxia survival. Plant Physiol. 2010; 153(2):757-72. PMC: 2879770. DOI: 10.1104/pp.110.155077. View

17.

Thirunavukkarasu N, Hossain F, Mohan S, Shiriga K, Mittal S, Sharma R . Genome-wide expression of transcriptomes and their co-expression pattern in subtropical maize (Zea mays L.) under waterlogging stress. PLoS One. 2013; 8(8):e70433. PMC: 3735631. DOI: 10.1371/journal.pone.0070433. View

18.

Fukao T, Xu K, Ronald P, Bailey-Serres J . A variable cluster of ethylene response factor-like genes regulates metabolic and developmental acclimation responses to submergence in rice. Plant Cell. 2006; 18(8):2021-34. PMC: 1533987. DOI: 10.1105/tpc.106.043000. View

19.

Voesenek L, Bailey-Serres J . Flooding tolerance: O2 sensing and survival strategies. Curr Opin Plant Biol. 2013; 16(5):647-53. DOI: 10.1016/j.pbi.2013.06.008. View

20.

Bradbury P, Zhang Z, Kroon D, Casstevens T, Ramdoss Y, Buckler E . TASSEL: software for association mapping of complex traits in diverse samples. Bioinformatics. 2007; 23(19):2633-5. DOI: 10.1093/bioinformatics/btm308. View