The cotton miR171a-SCL6 module mediates plant resistance through regulating GhPR1 expression

被引:7
|
作者
Hu, Guang [1 ,2 ]
Ge, Xiaoyang [1 ]
Wang, Peng [1 ]
Chen, Aimin [3 ]
Li, Fuguang [1 ]
Wu, Jiahe [2 ]
机构
[1] Chinese Acad Agr Sci, Inst Cotton Res, Natl Key Lab Cotton Biobreeding & Integrated Utili, Anyang 455000, Peoples R China
[2] Chinese Acad Sci, Inst Microbiol, State Key Lab Plant Genom, Beijing 100101, Peoples R China
[3] Join Hope Seeds Co Ltd, Minist Agr & Rural Affairs, Key Lab Creat Cotton Varieties Northwest, Changji 831100, Peoples R China
关键词
miR171a; SCL6; Verticillium wilt; Plant resistance; Gossypium hirsutum; CONTRIBUTES; ACCUMULATION; INTERACTS; DROUGHT; STRESS; GENES; ROLES;
D O I
10.1016/j.plaphy.2023.107995
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Plants have developed intricate defense mechanisms in response to fluctuating environmental cues, including the use of microRNA (miRNA) as post-transcriptional regulators. However, the specific mechanisms through which miRNA contributes to disease resistance remain largely elusive. While the miR171-SCLs have been investigated in an eclectic array of plants, there has been a notable scarcity of research specifically focused on cotton (Gossypium hirsutum). In our previous miRNA-sequencing analysis, we found that ghr-miR171a displayed a differential response to infections by Verticillium dahliae. In this study, we further investigated the function of the miR171a-SCL6 module in cotton during V. dahliae infection. The ghr-miR171a was confirmed to direct the cleavage of GhSCL6 mRNA in the post-transcriptional process, as evidenced by 5 ' RLM-RACE, beta-glucuronidase (GUS) histochemical staining and enzyme activity assay. Interestingly, we found that overexpressing ghrmiR171a reduced cotton plants' resistance to V. dahliae, while suppressing ghr-miR171a increased the plants' defense capacity. The GhSCL6 protein, when fused with green fluorescent protein (GFP), localizes in the cell nucleus, indicating its potential role in gene regulation. This was further corroborated by yeast two-hybrid assays, which verified GhSCL6's transcriptional activation ability. Through quantitative reverse transcriptase PCR (qRT-PCR), luciferase (LUC) fluorescence, and yeast one-hybrid assays, we found that GhSCL6 binds to the GTbox element of the GhPR1 promoter, activating its expression and thereby enhancing plant disease resistance. Taken together, our findings demonstrate that the cotton miR171a-SCL6 module regulates Verticillium wilt resistance in plants through the post-transcriptional process. This insight may offer new perspectives for disease resistance strategies in cotton.
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页数:10
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