Integrative Transcriptome Analysis of mRNA and miRNA in Pepper’s Response to Phytophthora capsici Infection

Author:

Li Yuan123,Wang Nan123,Guo Jianwen4,Zhou Xianjun123,Bai Xueyi123,Azeem Muhammad123ORCID,Zhu Liyun123,Chen Lin123,Chu Moli123,Wang Hui123,Cheng Wei123ORCID

Affiliation:

1. College of Life Sciences, Anhui Normal University, Wuhu 241000, China

2. Anhui Provincial Key Laboratory of Molecular Enzymology and Mechanism of Major Metabolic Diseases, Anhui Normal University, Wuhu 241000, China

3. Anhui Provincial Key Laboratory of the Conservation and Exploitation of Biological Resources, Anhui Normal University, Wuhu 241000, China

4. College of Agriculture, Fujian Agriculture and Forestry University, Fuzhou 350002, China

Abstract

Phytophthora blight of pepper is a notorious disease caused by the oomycete pathogen Phytophthora capsici, which poses a great threat to global pepper production. MicroRNA (miRNA) is a class of non-coding small RNAs that regulate gene expressions by altering the translation efficiency or stability of targeted mRNAs, which play important roles in the regulation of a plant’s response to pathogens. Herein, time-series mRNA-seq libraries and small RNA-seq libraries were constructed using pepper roots from the resistant line CM334 and the susceptible line EC01 inoculated with P. capsici at 0, 6, 24, and 48 h post-inoculation, respectively. For mRNA-seq analysis, a total of 2159 and 2971 differentially expressed genes (DEGs) were identified in CM334 and EC01, respectively. For miRNA-seq analysis, 491 pepper miRNAs were identified, including 330 known miRNAs and 161 novel miRNAs. Among them, 69 and 88 differentially expressed miRNAs (DEMs) were identified in CM334 and EC01, respectively. Examination of DEMs and their targets revealed 22 regulatory networks, predominantly featuring up-regulated miRNAs corresponding to down-regulated target genes. Notably, these DEM-DEG regulatory networks exhibited significant overlap between CM334 and EC01, suggesting that they might contribute to pepper’s basal defense against P. capsici. Furthermore, five selected DEMs (miR166, miR1171, miR395, miR530 and miRN2) and their target genes underwent qRT-PCR validation, confirming a consistent negative correlation in the expression patterns of miRNAs and their targets. This comprehensive analysis provides novel insights into the regulatory networks of miRNAs and their targets, offering valuable contributions to our understanding of pepper’s defense mechanisms against P. capsici.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Anhui Province, China

Outstanding Innovative Research Team for Molecular Enzymology and Detection in Anhui Provincial Universities

Anhui Provincial Key Laboratory of the Conservation and Exploitation of Biological Resources in Anhui Normal University

Publisher

MDPI AG

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