小麦E3酶TaPRP19参与了转基因Arabidopsis的干旱压力耐受性
Min Jeong Hong1, Chan Seop Ko1, Dae Yeon Kim2
1Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, 29 Geumgu, Jeongeup, 56212 Republic of Korea.
概括
小麦基因TaPRP19通过改善植物应激反应来增强干旱耐受性. 过度表达TaPRP19可以提高面临水资源短缺的作物中的抗氧化活性和存活率.
科学领域:
- 植物分子生物学 植物分子生物学
- 农作物科学 农作物科学
- 生物化学 生物化学
背景情况:
- 干旱压力对全球粮食安全构成重大威胁.
- 识别赋予干旱耐受性的基因对于作物改善至关重要.
研究的目的:
- 隔离和描述小麦U盒E3结合酶基因,TaPRP19,其在干旱应激耐受性中的作用.
- 阐明TaPRP19在减轻氧化应激的功能机制.
主要方法:
- 对TaPRP19.1的基因分离和表征.
- 亚细胞局部化和体外无化试验.
- 用RT-qPCR进行基因表达分析.
- 在压力条件下生成和分析转基因Arabidopsis.
主要成果:
- TaPRP19编码了一个具有无处不在活性的核局部化的U盒E3链酶.
- 干旱相关的压力 (PEG,曼尼托尔,ABA) 诱导了TaPRP19的表达.
- 在阿拉比多普西斯中,TaPRP19的过度表达增强了发芽,根生长和在压力下生存,伴随着高调的抗氧化防御和减少的ROS.
结论:
- TaPRP19在赋予植物干旱耐受性方面发挥着至关重要的作用.
- 通过增强氧化应激减轻机制,TaPRP19的功能.
- TaPRP19是通过基因工程开发耐旱小麦和其他作物的有希望的候选基因.
更多相关视频
10:27Functional Characterization of RING-Type E3 Ubiquitin Ligases In Vitro and In Planta
Published on: December 5, 2019
8.8K
10:40Comprehensive Workflow for the Genome-wide Identification and Expression Meta-analysis of the ATL E3 Ubiquitin Ligase Gene Family in Grapevine
Published on: December 22, 2017
10.4K
相关概念视频
Mismatch Repair
4.7K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
4.7K
Homologous Recombination
50.0K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
50.0K
Nucleotide Excision Repair
36.8K
Overview
36.8K
Long-patch Base Excision Repair
6.9K
Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
6.9K
Conservative Site-specific Recombination and Phase Variation
5.9K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
5.9K
