Cargando…
The PcMYB44‐mediated miR397‐ PcLACs module regulates defence‐induced lignification in pear resistance to fungal disease
Diseases caused by Alternaria alternata and Botryosphaeria dothidea diminish pear yield and quality, and restrict the pear agricultural industry. Lignification is a conserved mechanism for plant resistance against pathogen invasion. The regulatory mechanisms underlying defence‐induced lignification...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423334/ https://www.ncbi.nlm.nih.gov/pubmed/37312259 http://dx.doi.org/10.1111/mpp.13357 |
_version_ | 1785089425507614720 |
---|---|
author | Yang, Yuekun He, Ying Lv, Shamei Zhu, Haodong Wang, Tingting Wang, Guoping Hong, Ni Wang, Liping |
author_facet | Yang, Yuekun He, Ying Lv, Shamei Zhu, Haodong Wang, Tingting Wang, Guoping Hong, Ni Wang, Liping |
author_sort | Yang, Yuekun |
collection | PubMed |
description | Diseases caused by Alternaria alternata and Botryosphaeria dothidea diminish pear yield and quality, and restrict the pear agricultural industry. Lignification is a conserved mechanism for plant resistance against pathogen invasion. The regulatory mechanisms underlying defence‐induced lignification in pear in response to fungal pathogen infection remain unknown. In this study, analysis of lignification level and lignin content in pear revealed that A. alternata and B. dothidea induced lignification, and transcriptomics showed that lignin biosynthesis was affected. To explore whether laccases (LACs) mediated by miR397 regulate lignification in pear, we investigated the role of PcmiR397 in repressing the expression of PcLACs using 5′‐RNA ligase‐mediated‐RACE and co‐transformation in tobacco. Opposite expression patterns for PcmiR397 and PcLAC target genes were observed in pear in response to pathogens. Transient transformation in pear demonstrated that silencing PcmiR397 and overexpressing a single PcLAC enhanced resistance to pathogens via lignin synthesis. To further reveal the mechanism underpinning the PcMIR397 response of pear to pathogens, the PcMIR397 promoter was analysed, and pMIR397‐1039 was found to be inhibited by pathogen infection. The transcription factor PcMYB44 was up‐regulated, and it bound to the PcMIR397 promoter and inhibited transcription following pathogen infection. The results demonstrate the role of PcmiR397‐PcLACs in broad‐spectrum resistance to fungal disease, and the potential role of PcMYB44 involved in the miR397‐PcLAC module in regulating defence‐induced lignification. The findings provide valuable candidate gene resources and guidance for molecular breeding to improve resistance to fungal disease in pear. |
format | Online Article Text |
id | pubmed-10423334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104233342023-08-14 The PcMYB44‐mediated miR397‐ PcLACs module regulates defence‐induced lignification in pear resistance to fungal disease Yang, Yuekun He, Ying Lv, Shamei Zhu, Haodong Wang, Tingting Wang, Guoping Hong, Ni Wang, Liping Mol Plant Pathol Original Articles Diseases caused by Alternaria alternata and Botryosphaeria dothidea diminish pear yield and quality, and restrict the pear agricultural industry. Lignification is a conserved mechanism for plant resistance against pathogen invasion. The regulatory mechanisms underlying defence‐induced lignification in pear in response to fungal pathogen infection remain unknown. In this study, analysis of lignification level and lignin content in pear revealed that A. alternata and B. dothidea induced lignification, and transcriptomics showed that lignin biosynthesis was affected. To explore whether laccases (LACs) mediated by miR397 regulate lignification in pear, we investigated the role of PcmiR397 in repressing the expression of PcLACs using 5′‐RNA ligase‐mediated‐RACE and co‐transformation in tobacco. Opposite expression patterns for PcmiR397 and PcLAC target genes were observed in pear in response to pathogens. Transient transformation in pear demonstrated that silencing PcmiR397 and overexpressing a single PcLAC enhanced resistance to pathogens via lignin synthesis. To further reveal the mechanism underpinning the PcMIR397 response of pear to pathogens, the PcMIR397 promoter was analysed, and pMIR397‐1039 was found to be inhibited by pathogen infection. The transcription factor PcMYB44 was up‐regulated, and it bound to the PcMIR397 promoter and inhibited transcription following pathogen infection. The results demonstrate the role of PcmiR397‐PcLACs in broad‐spectrum resistance to fungal disease, and the potential role of PcMYB44 involved in the miR397‐PcLAC module in regulating defence‐induced lignification. The findings provide valuable candidate gene resources and guidance for molecular breeding to improve resistance to fungal disease in pear. John Wiley and Sons Inc. 2023-06-13 /pmc/articles/PMC10423334/ /pubmed/37312259 http://dx.doi.org/10.1111/mpp.13357 Text en © 2023 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Yang, Yuekun He, Ying Lv, Shamei Zhu, Haodong Wang, Tingting Wang, Guoping Hong, Ni Wang, Liping The PcMYB44‐mediated miR397‐ PcLACs module regulates defence‐induced lignification in pear resistance to fungal disease |
title | The PcMYB44‐mediated miR397‐
PcLACs module regulates defence‐induced lignification in pear resistance to fungal disease |
title_full | The PcMYB44‐mediated miR397‐
PcLACs module regulates defence‐induced lignification in pear resistance to fungal disease |
title_fullStr | The PcMYB44‐mediated miR397‐
PcLACs module regulates defence‐induced lignification in pear resistance to fungal disease |
title_full_unstemmed | The PcMYB44‐mediated miR397‐
PcLACs module regulates defence‐induced lignification in pear resistance to fungal disease |
title_short | The PcMYB44‐mediated miR397‐
PcLACs module regulates defence‐induced lignification in pear resistance to fungal disease |
title_sort | pcmyb44‐mediated mir397‐
pclacs module regulates defence‐induced lignification in pear resistance to fungal disease |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423334/ https://www.ncbi.nlm.nih.gov/pubmed/37312259 http://dx.doi.org/10.1111/mpp.13357 |
work_keys_str_mv | AT yangyuekun thepcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT heying thepcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT lvshamei thepcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT zhuhaodong thepcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT wangtingting thepcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT wangguoping thepcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT hongni thepcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT wangliping thepcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT yangyuekun pcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT heying pcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT lvshamei pcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT zhuhaodong pcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT wangtingting pcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT wangguoping pcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT hongni pcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease AT wangliping pcmyb44mediatedmir397pclacsmoduleregulatesdefenceinducedlignificationinpearresistancetofungaldisease |