Identification and characterization of GmMYB118 responses to drought and salt stress

被引:131
|
作者
Du, Yong-Tao [1 ]
Zhao, Meng-Jie [1 ]
Wang, Chang-Tao [2 ]
Gao, Yuan [1 ]
Wang, Yan-Xia [3 ]
Liu, Yong-Wei [4 ]
Chen, Ming [1 ]
Chen, Jun [1 ]
Zhou, Yong-Bin [1 ]
Xu, Zhao-Shi [1 ]
Ma, You-Zhi [1 ]
机构
[1] Chinese Acad Agr Sci, Natl Key Facil Crop Gene Resources & Genet Improv, Key Lab Biol & Genet Improvement Triticeae Crops, Inst Crop Sci,Minist Agr, Beijing 100081, Peoples R China
[2] Beijing Technol & Business Univ, Beijing Key Lab Plant Resource Res & Dev, Beijing Adv Innovat Ctr Food Nutr & Human Hlth, Beijing 100048, Peoples R China
[3] Shijiazhuang Acad Agr & Forestry Sci, Res Ctr Wheat Engn Technol Hebei, Shijiazhuang 050041, Hebei, Peoples R China
[4] Hebei Acad Agr & Forestry Sci, Inst Genet & Physiol, Plant Genet Engn Ctr Hebei Prov, Shijiazhuang 050051, Hebei, Peoples R China
来源
BMC PLANT BIOLOGY | 2018年 / 18卷
关键词
MYB transcription factor; Genome-wide analysis; Drought tolerance; Salt tolerance; CRISPR; Soybean; MYB TRANSCRIPTION FACTORS; MEDIATED TRANSFORMATION; GENE-EXPRESSION; ABSCISIC-ACID; FACTOR FAMILY; ARABIDOPSIS; TOLERANCE; ROOT; OVEREXPRESSION; PATHWAYS;
D O I
10.1186/s12870-018-1551-7
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
BackgroundAbiotic stress severely influences plant growth and development. MYB transcription factors (TFs), which compose one of the largest TF families, play an important role in abiotic stress responses.ResultWe identified 139 soybean MYB-related genes; these genes were divided into six groups based on their conserved domain and were distributed among 20 chromosomes (Chrs). Quantitative real-time PCR (qRT-PCR) indicated that GmMYB118 highly responsive to drought, salt and high temperature stress; thus, this gene was selected for further analysis. Subcellular localization revealed that the GmMYB118 protein located in the nucleus. Ectopic expression (EX) of GmMYB118 increased tolerance to drought and salt stress and regulated the expression of several stress-associated genes in transgenic Arabidopsis plants. Similarly, GmMYB118-overexpressing (OE) soybean plants generated via Agrobacterium rhizogenes (A. rhizogenes)-mediated transformation of the hairy roots showed improved drought and salt tolerance. Furthermore, compared with the control (CK) plants, the clustered, regularly interspaced, short palindromic repeat (CRISPR)-transformed plants exhibited reduced drought and salt tolerance. The contents of proline and chlorophyll in the OE plants were significantly greater than those in the CK plants, whose contents were greater than those in the CRISPR plants under drought and salt stress conditions. In contrast, the reactive oxygen species (ROS) and malondialdehyde (MDA) contents were significantly lower in the OE plants than in the CK plants, whose contents were lower than those in the CRISPR plants under stress conditions.ConclusionsThese results indicated that GmMYB118 could improve tolerance to drought and salt stress by promoting expression of stress-associated genes and regulating osmotic and oxidizing substances to maintain cell homeostasis.
引用
收藏
页数:18
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