Comparison of Transcriptome between Tolerant and Susceptible Rice Cultivar Reveals Positive and Negative Regulators of Response to Rhizoctonia solani in Rice
-
Published:2023-09-20
Issue:18
Volume:24
Page:14310
-
ISSN:1422-0067
-
Container-title:International Journal of Molecular Sciences
-
language:en
-
Short-container-title:IJMS
Author:
Yang Xiurong1ORCID, Yan Shuangyong2ORCID, Li Yuejiao1, Li Guangsheng1, Sun Shuqin1, Li Junling2, Cui Zhongqiu2, Huo Jianfei1, Sun Yue2, Wang Xiaojing2, Liu Fangzhou2
Affiliation:
1. Institute of Plant Protection, Tianjin Academy of Agricultural Sciences, Tianjin 300381, China 2. Institute of Crop Research, Tianjin Academy of Agricultural Sciences, Tianjin 300381, China
Abstract
Rice (Oryza sativa L.) is one of the world’s most crucial food crops, as it currently supports more than half of the world’s population. However, the presence of sheath blight (SB) caused by Rhizoctonia solani has become a significant issue for rice agriculture. This disease is responsible for causing severe yield losses each year and is a threat to global food security. The breeding of SB-resistant rice varieties requires a thorough understanding of the molecular mechanisms involved and the exploration of immune genes in rice. To this end, we conducted a screening of rice cultivars for resistance to SB and compared the transcriptome based on RNA-seq between the most tolerant and susceptible cultivars. Our study revealed significant transcriptomic differences between the tolerant cultivar ZhengDao 22 (ZD) and the most susceptible cultivar XinZhi No.1 (XZ) in response to R. solani invasion. Specifically, the tolerant cultivar showed 7066 differentially expressed genes (DEGs), while the susceptible cultivar showed only 60 DEGs. In further analysis, we observed clear differences in gene category between up- and down-regulated expression of genes (uDEGs and dDEGs) based on Gene Ontology (GO) classes in response to infection in the tolerant cultivar ZD, and then identified uDEGs related to cell surface pattern recognition receptors, the Ca2+ ion signaling pathway, and the Mitogen-Activated Protein Kinase (MAPK) cascade that play a positive role against R. solani. In addition, DEGs of the jasmonic acid and ethylene signaling pathways were mainly positively regulated, whereas DEGs of the auxin signaling pathway were mainly negatively regulated. Transcription factors were involved in the immune response as either positive or negative regulators of the response to this pathogen. Furthermore, our results showed that chloroplasts play a crucial role and that reduced photosynthetic capacity is a critical feature of this response. The results of this research have important implications for better characterization of the molecular mechanism of SB resistance and for the development of resistant cultivars through molecular breeding methods.
Funder
Tianjin Rice Research System—the Green Prevention and Control Project National Rice Variety Research Project Innovative Research for Young Scientists of Tianjin Academy of Agricultural Sciences
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis
Reference81 articles.
1. Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism;Chen;Nat. Genet.,2014 2. Emerging infectious diseases of plants: Pathogen pollution, climate change and agrotechnology drivers;Anderson;Trends Ecol. Evol.,2004 3. Shi, W., Zhao, S.-L., Liu, K., Sun, Y.-B., Ni, Z.-B., Zhang, G.-Y., Tang, H.-S., Zhu, J.-W., Wan, B.-J., and Sun, H.-Q. (2020). Comparison of leaf transcriptome in response to Rhizoctonia solani infection between resistant and susceptible rice cultivars. BMC Genom., 21. 4. Mapping and validation of QTLs for rice sheath blight resistance;Ozaki;Breed. Sci.,2013 5. Identification of defense-related genes in rice responding to challenge by Rhizoctonia solani;Zhao;Theor. Appl. Genet.,2008
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|