Genome-wide association analysis reveals a novel pathway mediated by a dual-TIR domain protein for pathogen resistance in cotton

Abstract Background Verticillium wilt is one of the most devasting diseases for many plants, leading to global economic loss. Cotton is known to be vulnerable to its fungal pathogen, Verticillium dahliae, yet the related genetic mechanism remains unknown. Results By genome-wide association studies o...

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Main Authors: Yihao Zhang, Yaning Zhang, Xiaoyang Ge, Yuan Yuan, Yuying Jin, Ye Wang, Lihong Zhao, Xiao Han, Wei Hu, Lan Yang, Chenxu Gao, Xi Wei, Fuguang Li, Zhaoen Yang
Format: Article
Language:English
Published: BMC 2023-05-01
Series:Genome Biology
Subjects:
Online Access:https://doi.org/10.1186/s13059-023-02950-9
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author Yihao Zhang
Yaning Zhang
Xiaoyang Ge
Yuan Yuan
Yuying Jin
Ye Wang
Lihong Zhao
Xiao Han
Wei Hu
Lan Yang
Chenxu Gao
Xi Wei
Fuguang Li
Zhaoen Yang
author_facet Yihao Zhang
Yaning Zhang
Xiaoyang Ge
Yuan Yuan
Yuying Jin
Ye Wang
Lihong Zhao
Xiao Han
Wei Hu
Lan Yang
Chenxu Gao
Xi Wei
Fuguang Li
Zhaoen Yang
author_sort Yihao Zhang
collection DOAJ
description Abstract Background Verticillium wilt is one of the most devasting diseases for many plants, leading to global economic loss. Cotton is known to be vulnerable to its fungal pathogen, Verticillium dahliae, yet the related genetic mechanism remains unknown. Results By genome-wide association studies of 419 accessions of the upland cotton, Gossypium hirsutum, we identify ten loci that are associated with resistance against Verticillium wilt. Among these loci, SHZDI1/SHZDP2/AYDP1 from chromosome A10 is located on a fragment introgressed from Gossypium arboreum. We characterize a large cluster of Toll/interleukin 1 (TIR) nucleotide-binding leucine-rich repeat receptors in this fragment. We then identify a dual-TIR domain gene from this cluster, GhRVD1, which triggers an effector-independent cell death and is induced by Verticillium dahliae. We confirm that GhRVD1 is one of the causal gene for SHZDI1. Allelic variation in the TIR domain attenuates GhRVD1-mediated resistance against Verticillium dahliae. Homodimerization between TIR1-TIR2 mediates rapid immune response, while disruption of its αD- and αE-helices interface eliminates the autoactivity and self-association of TIR1-TIR2. We further demonstrate that GhTIRP1 inhibits the autoactivity and self-association of TIR1-TIR2 by competing for binding to them, thereby preventing the resistance to Verticillium dahliae. Conclusions We propose the first working model for TIRP1 involved self-association and autoactivity of dual-TIR domain proteins that confer compromised pathogen resistance of dual-TIR domain proteins in plants. The findings reveal a novel mechanism on Verticillium dahliae resistance and provide genetic basis for breeding in future.
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spelling doaj.art-32154b0c1d7c449aa0cf8e6670a56b102023-05-14T11:18:37ZengBMCGenome Biology1474-760X2023-05-0124113110.1186/s13059-023-02950-9Genome-wide association analysis reveals a novel pathway mediated by a dual-TIR domain protein for pathogen resistance in cottonYihao Zhang0Yaning Zhang1Xiaoyang Ge2Yuan Yuan3Yuying Jin4Ye Wang5Lihong Zhao6Xiao Han7Wei Hu8Lan Yang9Chenxu Gao10Xi Wei11Fuguang Li12Zhaoen Yang13Zhengzhou Research Base, National Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Zhengzhou UniversityZhengzhou Research Base, National Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Zhengzhou UniversityNational Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Institute of Cotton Research, Chinese Academy of Agricultural SciencesNational Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Institute of Cotton Research, Chinese Academy of Agricultural SciencesNational Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Institute of Cotton Research, Chinese Academy of Agricultural SciencesNational Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Institute of Cotton Research, Chinese Academy of Agricultural SciencesNational Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Institute of Cotton Research, Chinese Academy of Agricultural SciencesNational Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Institute of Cotton Research, Chinese Academy of Agricultural SciencesZhengzhou Research Base, National Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Zhengzhou UniversityNational Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Institute of Cotton Research, Chinese Academy of Agricultural SciencesZhengzhou Research Base, National Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Zhengzhou UniversityNational Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Institute of Cotton Research, Chinese Academy of Agricultural SciencesZhengzhou Research Base, National Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Zhengzhou UniversityZhengzhou Research Base, National Key Laboratory of Cotton Bio-breeding and Integrated Utilization, Zhengzhou UniversityAbstract Background Verticillium wilt is one of the most devasting diseases for many plants, leading to global economic loss. Cotton is known to be vulnerable to its fungal pathogen, Verticillium dahliae, yet the related genetic mechanism remains unknown. Results By genome-wide association studies of 419 accessions of the upland cotton, Gossypium hirsutum, we identify ten loci that are associated with resistance against Verticillium wilt. Among these loci, SHZDI1/SHZDP2/AYDP1 from chromosome A10 is located on a fragment introgressed from Gossypium arboreum. We characterize a large cluster of Toll/interleukin 1 (TIR) nucleotide-binding leucine-rich repeat receptors in this fragment. We then identify a dual-TIR domain gene from this cluster, GhRVD1, which triggers an effector-independent cell death and is induced by Verticillium dahliae. We confirm that GhRVD1 is one of the causal gene for SHZDI1. Allelic variation in the TIR domain attenuates GhRVD1-mediated resistance against Verticillium dahliae. Homodimerization between TIR1-TIR2 mediates rapid immune response, while disruption of its αD- and αE-helices interface eliminates the autoactivity and self-association of TIR1-TIR2. We further demonstrate that GhTIRP1 inhibits the autoactivity and self-association of TIR1-TIR2 by competing for binding to them, thereby preventing the resistance to Verticillium dahliae. Conclusions We propose the first working model for TIRP1 involved self-association and autoactivity of dual-TIR domain proteins that confer compromised pathogen resistance of dual-TIR domain proteins in plants. The findings reveal a novel mechanism on Verticillium dahliae resistance and provide genetic basis for breeding in future.https://doi.org/10.1186/s13059-023-02950-9Verticillium fungi; GWAS; Introgression; NLR receptors; Autoactivity; Self-association
spellingShingle Yihao Zhang
Yaning Zhang
Xiaoyang Ge
Yuan Yuan
Yuying Jin
Ye Wang
Lihong Zhao
Xiao Han
Wei Hu
Lan Yang
Chenxu Gao
Xi Wei
Fuguang Li
Zhaoen Yang
Genome-wide association analysis reveals a novel pathway mediated by a dual-TIR domain protein for pathogen resistance in cotton
Genome Biology
Verticillium fungi; GWAS; Introgression; NLR receptors; Autoactivity; Self-association
title Genome-wide association analysis reveals a novel pathway mediated by a dual-TIR domain protein for pathogen resistance in cotton
title_full Genome-wide association analysis reveals a novel pathway mediated by a dual-TIR domain protein for pathogen resistance in cotton
title_fullStr Genome-wide association analysis reveals a novel pathway mediated by a dual-TIR domain protein for pathogen resistance in cotton
title_full_unstemmed Genome-wide association analysis reveals a novel pathway mediated by a dual-TIR domain protein for pathogen resistance in cotton
title_short Genome-wide association analysis reveals a novel pathway mediated by a dual-TIR domain protein for pathogen resistance in cotton
title_sort genome wide association analysis reveals a novel pathway mediated by a dual tir domain protein for pathogen resistance in cotton
topic Verticillium fungi; GWAS; Introgression; NLR receptors; Autoactivity; Self-association
url https://doi.org/10.1186/s13059-023-02950-9
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