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利用 CRISPR/Cas9 技术生成的 敲除突变体提高了水稻的非生物胁迫耐受性。

Knockout Mutants of Generated Using CRISPR/Cas9 Revealed Abiotic Stress Tolerance in Rice.

机构信息

Department of Crop Science, College of Agriculture and Life & Environment Sciences, Chungbuk National University, Cheongju 28644, Republic of Korea.

Division of Horticultural Biotechnology, Hankyong National University, Anseong 17579, Republic of Korea.

出版信息

Int J Mol Sci. 2023 Mar 10;24(6):5338. doi: 10.3390/ijms24065338.

DOI:10.3390/ijms24065338
PMID:36982409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10048836/
Abstract

Plants produce and accumulate stress-resistant substances when exposed to abiotic stress, which involves a protein conversion mechanism that breaks down stress-damaged proteins and supplies usable amino acids. Eukaryotic protein turnover is mostly driven by the ubiquitination pathway. Among the three enzymes required for protein degradation, E3 ubiquitin ligase plays a pivotal role in most cells, as it determines the specificity of ubiquitination and selects target proteins for degradation. In this study, to investigate the function of (Plant U-box gene in ), we constructed a CRISPR/Cas9 vector, generated gene-edited individuals, and evaluated resistance to abiotic stress using gene-edited lines. A stress-tolerant phenotype was observed as a result of drought and salinity stress treatment in the T gene-edited null lines (PUB7-GE) lacking the T-DNA. In addition, although PUB7-GE did not show any significant change in mRNA expression analysis, it showed lower ion leakage and higher proline content than the wild type (WT). Protein-protein interaction analysis revealed that the expression of the genes (, , , and ) known to be involved in stress increased in PUB7-GE and this, by forming a 1-node network with and , acted as a negative regulator of drought and salinity stress. This result provides evidence that will be a useful target for both breeding and future research on drought tolerance/abiotic stress in rice.

摘要

当植物受到非生物胁迫时,会产生并积累具有抗逆性的物质,这涉及到一种蛋白质转换机制,该机制可分解应激损伤的蛋白质并提供可用的氨基酸。真核生物的蛋白质周转主要由泛素化途径驱动。在三种参与蛋白质降解的酶中,E3 泛素连接酶在大多数细胞中起着关键作用,因为它决定了泛素化的特异性,并选择靶蛋白进行降解。在这项研究中,为了研究 (植物 U-box 基因在)的功能,我们构建了一个 CRISPR/Cas9 载体,生成了基因编辑个体,并使用基因编辑系评估了对非生物胁迫的抗性。在缺乏 T-DNA 的 T 基因编辑缺失系(PUB7-GE)中,观察到对干旱和盐胁迫处理的耐受力表型。此外,尽管 PUB7-GE 在 mRNA 表达分析中没有显示任何显著变化,但与野生型(WT)相比,它显示出较低的离子泄漏和较高的脯氨酸含量。蛋白质-蛋白质相互作用分析表明,与胁迫相关的基因(、、、和)的表达在 PUB7-GE 中增加,并且通过与和形成 1 个节点网络,作为干旱和盐胁迫的负调节剂。这一结果表明, 将成为水稻耐旱性/非生物胁迫育种和未来研究的有用目标。

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