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Lysine crotonylation of DgTIL1 at K72 modulates cold tolerance by enhancing DgnsLTP stability in chrysanthemum
Lysine crotonylation of proteins is a recently identified post‐translational modification (PTM) in plants. However, the function of lysine‐crotonylated proteins in response to abiotic stress in plants has not been reported. In this study, we identified a temperature‐induced lipocalin‐1‐like gene (Dg...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196654/ https://www.ncbi.nlm.nih.gov/pubmed/33368971 http://dx.doi.org/10.1111/pbi.13533 |
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author | Huang, Qiuxiang Liao, Xiaoqin Yang, Xiaohan Luo, Yunchen Lin, Ping Zeng, Qinhan Bai, Huiru Jiang, Beibei Pan, Yuanzhi Zhang, Fan Zhang, Lei Jia, Yin Liu, Qinglin |
author_facet | Huang, Qiuxiang Liao, Xiaoqin Yang, Xiaohan Luo, Yunchen Lin, Ping Zeng, Qinhan Bai, Huiru Jiang, Beibei Pan, Yuanzhi Zhang, Fan Zhang, Lei Jia, Yin Liu, Qinglin |
author_sort | Huang, Qiuxiang |
collection | PubMed |
description | Lysine crotonylation of proteins is a recently identified post‐translational modification (PTM) in plants. However, the function of lysine‐crotonylated proteins in response to abiotic stress in plants has not been reported. In this study, we identified a temperature‐induced lipocalin‐1‐like gene (DgTIL1) from chrysanthemum and showed that it was notably induced in response to cold stress. Overexpression of DgTIL1 enhanced cold tolerance in transgenic chrysanthemum. Ubiquitin membrane yeast two‐hybrid (MYTH) system and bimolecular fluorescence complementation (BIFC) assays showed that DgTIL1 interacts with a nonspecific lipid transfer protein (DgnsLTP), which can promote peroxidase (POD) gene expression and POD activity to reduce the accumulation of reactive oxygen species (ROS) and improve resistance to cold stress in DgnsLTP transgenic chrysanthemum. In addition, we found that DgTIL1 was lysine crotonylated at K72 in response to low temperature in chrysanthemum. Moreover, lysine crotonylation of DgTIL1 prevented DgnsLTP protein degradation in tobacco and chrysanthemum. Inhibition of DgnsLTP degradation by lysine crotonylation of DgTIL1 further enhanced POD expression and POD activity, reduced the accumulation of ROS under cold stress in DgTIL1 transgenic chrysanthemum, thus promoting the cold resistance of chrysanthemum. |
format | Online Article Text |
id | pubmed-8196654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81966542021-06-15 Lysine crotonylation of DgTIL1 at K72 modulates cold tolerance by enhancing DgnsLTP stability in chrysanthemum Huang, Qiuxiang Liao, Xiaoqin Yang, Xiaohan Luo, Yunchen Lin, Ping Zeng, Qinhan Bai, Huiru Jiang, Beibei Pan, Yuanzhi Zhang, Fan Zhang, Lei Jia, Yin Liu, Qinglin Plant Biotechnol J Research Articles Lysine crotonylation of proteins is a recently identified post‐translational modification (PTM) in plants. However, the function of lysine‐crotonylated proteins in response to abiotic stress in plants has not been reported. In this study, we identified a temperature‐induced lipocalin‐1‐like gene (DgTIL1) from chrysanthemum and showed that it was notably induced in response to cold stress. Overexpression of DgTIL1 enhanced cold tolerance in transgenic chrysanthemum. Ubiquitin membrane yeast two‐hybrid (MYTH) system and bimolecular fluorescence complementation (BIFC) assays showed that DgTIL1 interacts with a nonspecific lipid transfer protein (DgnsLTP), which can promote peroxidase (POD) gene expression and POD activity to reduce the accumulation of reactive oxygen species (ROS) and improve resistance to cold stress in DgnsLTP transgenic chrysanthemum. In addition, we found that DgTIL1 was lysine crotonylated at K72 in response to low temperature in chrysanthemum. Moreover, lysine crotonylation of DgTIL1 prevented DgnsLTP protein degradation in tobacco and chrysanthemum. Inhibition of DgnsLTP degradation by lysine crotonylation of DgTIL1 further enhanced POD expression and POD activity, reduced the accumulation of ROS under cold stress in DgTIL1 transgenic chrysanthemum, thus promoting the cold resistance of chrysanthemum. John Wiley and Sons Inc. 2021-01-21 2021-06 /pmc/articles/PMC8196654/ /pubmed/33368971 http://dx.doi.org/10.1111/pbi.13533 Text en © 2020 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Huang, Qiuxiang Liao, Xiaoqin Yang, Xiaohan Luo, Yunchen Lin, Ping Zeng, Qinhan Bai, Huiru Jiang, Beibei Pan, Yuanzhi Zhang, Fan Zhang, Lei Jia, Yin Liu, Qinglin Lysine crotonylation of DgTIL1 at K72 modulates cold tolerance by enhancing DgnsLTP stability in chrysanthemum |
title | Lysine crotonylation of DgTIL1 at K72 modulates cold tolerance by enhancing DgnsLTP stability in chrysanthemum |
title_full | Lysine crotonylation of DgTIL1 at K72 modulates cold tolerance by enhancing DgnsLTP stability in chrysanthemum |
title_fullStr | Lysine crotonylation of DgTIL1 at K72 modulates cold tolerance by enhancing DgnsLTP stability in chrysanthemum |
title_full_unstemmed | Lysine crotonylation of DgTIL1 at K72 modulates cold tolerance by enhancing DgnsLTP stability in chrysanthemum |
title_short | Lysine crotonylation of DgTIL1 at K72 modulates cold tolerance by enhancing DgnsLTP stability in chrysanthemum |
title_sort | lysine crotonylation of dgtil1 at k72 modulates cold tolerance by enhancing dgnsltp stability in chrysanthemum |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196654/ https://www.ncbi.nlm.nih.gov/pubmed/33368971 http://dx.doi.org/10.1111/pbi.13533 |
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