Transcriptome analysis reveals the effect of acidic environment on adventitious root differentiation in Camellia sinensis
文献类型: 外文期刊
作者: Liu, Kai 1 ; Zhao, Yichen 1 ; Zhao, De-Gang 1 ;
作者机构: 1.Guizhou Univ, Coll Tea Sci, Key Lab Plant Resources Conservat & Germplasm Inno, Coll Life Sci,Minist Educ,Inst Agrobioengn, Guiyang 550025, Peoples R China
2.Guizhou Acad Agr Sci, Plant Conservat Technol Ctr, Guizhou Key Lab Agr Biotechnol, Guiyang 550006, Peoples R China
关键词: Tea plants; Acid environment; Adventitious root differentiation; Phytohormone
期刊名称:PLANT MOLECULAR BIOLOGY ( 影响因子:5.1; 五年影响因子:5.3 )
ISSN: 0167-4412
年卷期: 2023 年
页码:
收录情况: SCI
摘要: The generation of adventitious roots (ARs) is the key to the success of cuttings. The appropriate environment for AR differentiation in tea plants is acidic. However, the mechanism is unclear. In this study, pH 4.5 was suitable condition for the differentiation of AR in tea plants. At the base of cuttings, the root primordia differentiated ARs more rapidly at pH 4.5 than pH 7.0, and nine AR differentiation-related genes were found to be differentially expressed in 30 days, the result was also validated by qRT-PCR. The promoter regions of these genes contained auxin and brassinosteroid response elements. The expression levels of several genes which were involved in auxin and brassinosteroid synthesis as well as signaling at pH 4.5 compared to pH 7.0 occurred differential expression. Brassinolide (BL) and indole-3-acetic acid (IAA) could affect the differentiation of ARs under pH 4.5 and pH 7.0. By qRT-PCR analysis of genes during ARs generation, BL and IAA inhibited and promoted the expression of CsIAA14 gene, respectively, to regulate auxin signal transduction. Meanwhile, the expression levels of CsKNAT4, CsNAC2, CsNAC100, CsWRKY30 and CsLBD18 genes were up-regulated upon auxin treatment and were positively correlated with ARs differentiation.This study showed that pH 4.5 was the most suitable environment for the root primordia differentiation of AR in tea plant. Proper acidic pH conditions promoted auxin synthesis and signal transduction. The auxin initiated the expression of AR differentiation-related genes, and promoted its differentiated. BL was involved in ARs formation and elongation by regulating auxin signal transduction.
- 相关文献
作者其他论文 更多>>
-
Cloning and functional characterization of the peptide deformylase encoding gene EuPDF1B from Eucommia ulmoides Oliv
作者:Wang, Yumei;Zhao, De-Gang;Zhao, De-Gang
关键词:Peptide deformylase; Promoter; Transgenic plants
-
Overexpression of the Eucommia ulmoides chitinase EuCHIT73.88 gene improves tobacco disease resistance
作者:Li, Xiao-man;Zhao, De-Gang;Chen, Xi;Zhao, De-Gang
关键词:Gene cloning; Black shank disease; Eucommia chitinase; Disease resistance
-
Tea plant (3-1, 4-glucanase enhances the propagation of Camellia tachangensis F. C. Zhang by promoting graft wound healing
作者:Ren, Na;Cheng, Linan;Zhao, Yichen;Zhao, De-gang;Zhao, Yichen;Zhao, De-gang;Zhao, De-gang
关键词:Ancient tea plants; Camellia tachangensis; (3-1; 4 glucanase; Grafting; Tea quality
-
Cloning and functional characterization of the legumin A gene (EuLEGA) from Eucommia ulmoides Oliver
作者:Zheng, Lina;Zhao, De-Gang;Zheng, Lina;Zhao, De-Gang
关键词:Eucommia ulmoides; Legumin A; Legumin A-encoding gene; Transgene
-
Cloning and Function Identification of a Phytoene Desaturase Gene from Eucommia ulmoides
作者:Wang, Jiali;Chen, Xiangmei;Huang, Xiaozhen;Zhao, Yichen;Zhao, Degang;Zhao, Degang
关键词:Eucommia ulmoides; EuPDS; virus-induced gene silencing; TRV; relative expression
-
Overexpression of β-1,4-Glucanase Gene EuEG1 Improves Micrografting of Eucommia ulmoides
作者:Wang, Lei;Wang, Runying;Zhao, Yichen;Zhao, Degang;Zhao, Degang;Li, Yi
关键词:Eucommia ulmoides; genetic transformation; EuEG1 gene; micrografting
-
Transcriptome analysis reveals the effect of grafting on gossypol biosynthesis and gland formation in cotton
作者:Ye, Kun;Teng, Teng;Yang, Teng;Zhao, Degang;Zhao, Yichen;Zhao, Degang
关键词:Cotton; Grafting; Pigment gland density; Gossypol content; Gossypol synthesis related genes; Transcriptome analysis; Differentially expressed genes; Real-time PCR analysis