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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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