lncRNA7 and lncRNA2 modulate cell wall defense genes to regulate cotton resistance to Verticillium wilt

Author:

Zhang Lin12,Liu Jinlei1,Cheng Jieru1ORCID,Sun Quan13ORCID,Zhang Yu1ORCID,Liu Jinggao4ORCID,Li Huimin1,Zhang Zhen1,Wang Ping1,Cai Chaowei1,Chu Zongyan5,Zhang Xiao1,Yuan Youlu6,Shi Yuzhen6ORCID,Cai Yingfan1ORCID

Affiliation:

1. State Key Laboratory of Cotton Biology, Henan Key Laboratory of Plant Stress Biology, School of Life Sciences, School of Computer and Information Engineering, Henan University, Kaifeng 475001, China

2. College of life science and agricultural engineering, Nanyang Normal University, Nanyang 473000, China

3. Chongqing Key Laboratory of Big Data for Bio Intelligence, College of Bioinformation, Chongqing University of Posts and Telecommunications, Chongqing 400065, China

4. Southern Plains Agricultural Research Center, Agricultural Research Service, USDA, College Station, Texas 77845, USA

5. Kaifeng Academy of Agriculture and Forestry, Kaifeng 475000, China

6. State Key Laboratory of Cotton Biology, Key Laboratory of Biological and Genetic Breeding of Cotton, The Ministry of Agriculture, Institute of Cotton Research, Chinese Academy of Agricultural Sciences, Anyang 455000, China

Abstract

Abstract In plants, long noncoding RNAs (lncRNAs) regulate disease resistance against fungi and other pathogens. However, the specific mechanism behind this regulation remains unclear. In this study, we identified disease resistance-related lncRNAs as well as their regulating genes and assessed their functions by infection of cotton (Gossypium) chromosome segment substitution lines with Verticillium dahliae. Our results demonstrated that lncRNA7 and its regulating gene Pectin methylesterase inhibitor 13 (GbPMEI13) positively regulated disease resistance via the silencing approach, while ectopic overexpression of GbPMEI13 in Arabidopsis (Arabidopsis thaliana) promoted growth and enhanced resistance to V. dahliae. In contrast, lncRNA2 and its regulating gene Polygalacturonase 12 (GbPG12) negatively regulated resistance to V. dahliae. We further found that fungal disease-related agents, including the pectin-derived oligogalacturonide (OG), could downregulate the expression of lncRNA2 and GbPG12, leading to pectin accumulation. Conversely, OG upregulated the expression of lncRNA7, which encodes a plant peptide phytosulfokine (PSK-α), which was confirmed by lncRNA7 overexpression and Ultra Performance Liquid Chromatography Tandem Mass Spectrometry (UPLC-MS) experiments. We showed that PSK-α promoted 3-Indoleacetic acid (IAA) accumulation and activated GbPMEI13 expression through Auxin Response Factor 5. Since it is an inhibitor of pectin methylesterase (PME), GbPMEI13 promotes pectin methylation and therefore increases the resistance to V. dahliae. Consistently, we also demonstrated that GbPMEI13 inhibits the mycelial growth and spore germination of V. dahliae in vitro. In this study, we demonstrated that lncRNA7, lncRNA2, and their regulating genes modulate cell wall defense against V. dahliae via auxin-mediated signaling, providing a strategy for cotton breeding.

Funder

Henan Natural Science Foundation

Natural Science Foundation of China (NSFC

National Key Research and Development Program of China

Innovation and Talent Introduction Program on Crop Stress Biology

Science and Technology Research Program of Chongqing Municipal Education Commission

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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