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Cloning and characterization of two chlorophyll A/B binding protein genes and analysis of their gene family in Camellia sinensis
In this study, two chlorophyll A/B binding protein (CAB) genes (CsCP1 and CsCP2) in tea plant were cloned. The proteins encoded by these genes belong to the external or internal antenna proteins of PS II, respectively. They may be the targets of physiological regulation for tea leaf cell PS II becau...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067855/ https://www.ncbi.nlm.nih.gov/pubmed/32165676 http://dx.doi.org/10.1038/s41598-020-61317-3 |
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author | Li, Xian-Wen Zhu, Yu-Lin Chen, Chu-Yan Geng, Zhi-Juan Li, Xiang-Yong Ye, Ting-Ting Mao, Xiao-Nan Du, Fang |
author_facet | Li, Xian-Wen Zhu, Yu-Lin Chen, Chu-Yan Geng, Zhi-Juan Li, Xiang-Yong Ye, Ting-Ting Mao, Xiao-Nan Du, Fang |
author_sort | Li, Xian-Wen |
collection | PubMed |
description | In this study, two chlorophyll A/B binding protein (CAB) genes (CsCP1 and CsCP2) in tea plant were cloned. The proteins encoded by these genes belong to the external or internal antenna proteins of PS II, respectively. They may be the targets of physiological regulation for tea leaf cell PS II because they all contain multiple functional domains and modifiable sites. The CAB gene family in the tea genome consists of 25 homologous genes. We measured the expression patterns of ten genes in the CsCP1 and CsCP2 subfamily under six different stresses. CsCP1 expression was inhibited in response to 6 kinds of stress; CsCP2 expression was slightly upregulated only after cold stress and ABA treatment. However, the expression levels of CSA016997 and CSA030476 were upregulated significantly in the six stresses. The results suggested that the 10 CAB genes may have different functions in tea leaves. Moreover, changes in the expression of the 10 genes under stress appear to be related to ABA- and MeJA-dependent signalling pathways, and their responses to MeJA treatment is faster than those to ABA. In addition, we introduced our experiences for cloning the genes in the context of complex genomes. |
format | Online Article Text |
id | pubmed-7067855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70678552020-03-19 Cloning and characterization of two chlorophyll A/B binding protein genes and analysis of their gene family in Camellia sinensis Li, Xian-Wen Zhu, Yu-Lin Chen, Chu-Yan Geng, Zhi-Juan Li, Xiang-Yong Ye, Ting-Ting Mao, Xiao-Nan Du, Fang Sci Rep Article In this study, two chlorophyll A/B binding protein (CAB) genes (CsCP1 and CsCP2) in tea plant were cloned. The proteins encoded by these genes belong to the external or internal antenna proteins of PS II, respectively. They may be the targets of physiological regulation for tea leaf cell PS II because they all contain multiple functional domains and modifiable sites. The CAB gene family in the tea genome consists of 25 homologous genes. We measured the expression patterns of ten genes in the CsCP1 and CsCP2 subfamily under six different stresses. CsCP1 expression was inhibited in response to 6 kinds of stress; CsCP2 expression was slightly upregulated only after cold stress and ABA treatment. However, the expression levels of CSA016997 and CSA030476 were upregulated significantly in the six stresses. The results suggested that the 10 CAB genes may have different functions in tea leaves. Moreover, changes in the expression of the 10 genes under stress appear to be related to ABA- and MeJA-dependent signalling pathways, and their responses to MeJA treatment is faster than those to ABA. In addition, we introduced our experiences for cloning the genes in the context of complex genomes. Nature Publishing Group UK 2020-03-12 /pmc/articles/PMC7067855/ /pubmed/32165676 http://dx.doi.org/10.1038/s41598-020-61317-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Li, Xian-Wen Zhu, Yu-Lin Chen, Chu-Yan Geng, Zhi-Juan Li, Xiang-Yong Ye, Ting-Ting Mao, Xiao-Nan Du, Fang Cloning and characterization of two chlorophyll A/B binding protein genes and analysis of their gene family in Camellia sinensis |
title | Cloning and characterization of two chlorophyll A/B binding protein genes and analysis of their gene family in Camellia sinensis |
title_full | Cloning and characterization of two chlorophyll A/B binding protein genes and analysis of their gene family in Camellia sinensis |
title_fullStr | Cloning and characterization of two chlorophyll A/B binding protein genes and analysis of their gene family in Camellia sinensis |
title_full_unstemmed | Cloning and characterization of two chlorophyll A/B binding protein genes and analysis of their gene family in Camellia sinensis |
title_short | Cloning and characterization of two chlorophyll A/B binding protein genes and analysis of their gene family in Camellia sinensis |
title_sort | cloning and characterization of two chlorophyll a/b binding protein genes and analysis of their gene family in camellia sinensis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067855/ https://www.ncbi.nlm.nih.gov/pubmed/32165676 http://dx.doi.org/10.1038/s41598-020-61317-3 |
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