Identification, Molecular Characteristic, and Expression Analysis of PIFs Related to Chlorophyll Metabolism in Tea Plant (Camellia sinensis)

被引:8
|
作者
Zhang, Xiangna [1 ]
Xiong, Ligui [1 ,2 ]
Luo, Yong [3 ]
Wen, Beibei [1 ]
Wang, Kunbo [1 ,2 ]
Liu, Zhonghua [1 ,2 ]
Huang, Jian-an [1 ,2 ]
Li, Juan [1 ,2 ]
机构
[1] Hunan Agr Univ, Key Lab Tea Sci, Minist Educ, Changsha 410128, Peoples R China
[2] Hunan Agr Univ, Natl Res Ctr Engn Technol Utilizat Funct Ingredie, Coinnovat Ctr Utilizat Funct Ingredients Botan, Changsha 410128, Peoples R China
[3] Xiangnan Univ, Sch Chem & Environm Sci, Chenzhou 423043, Peoples R China
基金
中国国家自然科学基金;
关键词
Camellia sinensis; phytochrome-interacting factors; transcription factors; chlorophyll; gene expression; PHYTOCHROME-INTERACTING FACTOR; MG-CHELATASE; BIOSYNTHESIS; ARABIDOPSIS; LIGHT; PROTEINS;
D O I
10.3390/ijms222010949
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The phytochrome-interacting factors (PIFs) proteins belong to the subfamily of basic helixloop-helix (bHLH) transcription factors and play important roles in chloroplast development and chlorophyll biosynthesis. Currently, knowledge about the PIF gene family in Camellia sinensis remains very limited. In this study, seven PIF members were identified in the C. sinensis genome and named based on homology with AtPIF genes in Arabidopsis thaliana. All C. sinensis PIF (CsPIF) proteins have both the conserved active PHYB binding (APB) and bHLH domains. Phylogenetic analysis revealed that CsPIFs were clustered into four groups-PIF1, PIF3, PIF7, and PIF8-and most CsPIFs were clustered in pairs with their corresponding orthologs in Populus tremula. CsPIF members in the same group tended to display uniform or similar exon-intron distribution patterns and motif compositions. CsPIF genes were differentially expressed in C. sinensis with various leaf colors and strongly correlated with the expression of genes involved in the chlorophyll metabolism pathway. Promoter analysis of structural genes related to chlorophyll metabolism found DNA-binding sites of PIFs were abundant in the promoter regions. Protein-protein interaction networks of CsPIFs demonstrated a close association with phytochrome, PIF4, HY5, TOC1, COP1, and PTAC12 proteins. Additionally, subcellular localization and transcriptional activity analysis suggested that CsPIF3b was nuclear localized protein and possessed transcriptional activity. We also found that CsPIF3b could activate the transcription of CsHEMA and CsPOR in Nicotiana benthamiana leaves. This work provides comprehensive research of CsPIFs and would be helpful to further promote the regulation mechanism of PIF on chlorophyll metabolism in C. sinensis.
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页数:15
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