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Expression Pattern and Functional Analysis of MebHLH149 Gene in Response to Cassava Bacterial Blight
Thursday, 2024/11/07 | 08:39:51

Min CuiFeifei AnSongbi ChenXindao Qin

Plants (Basel); 2024 Aug 30; 13(17):2422. doi: 10.3390/plants13172422.

Abstract

The significant reduction in cassava (Manihot esculenta Crantz) yields attributed to cassava bacterial blight (CBB) constitutes an urgent matter demanding prompt attention. The current study centered on the MebHLH149 transcription factor, which is acknowledged to be reactive to CBB and exhibits augmented expression levels, as indicated by laboratory transcriptome data. Our exploration, encompassing Xanthomonas phaseoli pv. manihotis strain CHN01 (Xpm CHN01) and hormone stress, disclosed that the MebHLH149 gene interacts with the pathogen at the early stage of infection. Furthermore, the MebHLH149 gene has been discovered to be responsive to the plant hormones abscisic acid (ABA), methyl jasmonate (MeJA), and salicylic acid (SA), intimating a potential role in the signaling pathways mediated by these hormones. An analysis of the protein's subcellular localization suggested that MebHLH149 is predominantly located within the nucleus. Through virus-induced gene silencing (VIGS) in cassava, we discovered that MebHLH149-silenced plants manifested higher disease susceptibility, less ROS accumulation, and significantly larger leaf spot areas compared to control plants. The proteins MePRE5 and MePRE6, which are predicted to interact with MebHLH149, demonstrated complementary downregulation and upregulation patterns in response to silencing and overexpression of the MebHLH149 gene. This implies a potential interaction between MebHLH149 and these proteins. Both MePRE5 and MePRE6 genes are involved in the initial immune response to CBB. Notably, MebHLH149 was identified as a protein that physically interacts with MePRE5 and MePRE6. Based on these findings, it is hypothesized that the MebHLH149 gene likely functions as a positive regulator in the defense mechanisms of cassava against CBB.

 

See https://pubmed.ncbi.nlm.nih.gov/39273906/

 

Figure 3:

Silencing of MebHLH149 gene: (a) phenotypes of MebHLH149-silenced cassava plants captured on the 26th day after MebHLH149 gene silencing; (b) detection of MebHLH149 gene silencing efficiency; (c) phenotypes of cassava plants after MebHLH149 gene silencing and inoculation with Xpm CHN01; (d) statistical analysis of lesion area; (e) statistical analysis of bacterial count. pCsCMV-ChlI345 represents the positive control; pCsCMV-NC represents the negative control; pCsCMV-MebHLH149 represents the experimental group. All experiments were conducted with three independent biological replicates, and the analysis was performed using the 2−ΔΔCt method. Significant differences are indicated as follows: * p < 0.05 and ** p < 0.01. Significant differences were assessed using ANOVA and Dunnett’s test.

 

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