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通过基因工程改造乙烯应答因子SlERF.J2培育耐旱耐盐番茄种质

Eng Life Sci · 2026年6月27日 · Chen 等 11 位作者

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一分钟了解要点用CRISPR敲除番茄SlERF.J2基因,获得耐旱耐盐性增强的番茄材料。安全研究者利用CRISPR/Cas9基因编辑技术(一种精准修改基因的方法)构建了slerf.j2敲除番茄株系,发现敲除后番茄幼苗对聚乙二醇6000模拟的干旱、甘露醇和盐胁迫的耐受性明显增强。结果与野生型相比,敲除株系的过氧化物酶活性和叶片相对含水量显著升高,过氧化氢和丙二醛含量显著降低,多个胁迫响应、类黄酮合成、叶绿素合成和激素合成相关基因表达也更高。

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Drought and salinity are key abiotic constraints limiting the growth, development, and yield of tomato (Solanum lycopersicum). Ethylene response factors are crucial regulators that govern plants' adaptation to diverse abiotic and biotic stress stimuli. Nevertheless, the exact role of SlERF.J2 in abiotic stress resistance remains unclear. In this study, clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 gene-editing technology was used to generate slerf.j2 knockout tomato lines to clarify the biological function of SlERF.J2 in regulating tomato's responses to drought and salt stress. The results revealed that deletion of SlERF.J2 markedly enhanced tomato seedlings' resistance to polyethylene glycol 6000-induced drought, mannitol, and salt stresses. Compared with the wild-type (WT), the knockout lines exhibited significantly increased peroxidase activity and leaf relative water content, as well as markedly decreased contents of hydrogen peroxide and malondialdehyde. After stress treatment, the expression levels of genes associated with the stress response, flavonoid biosynthesis, chlorophyll biosynthesis, light response, cell division, and hormone biosynthesis in SlERF.J2-edited tomato lines were significantly higher than those in WT plants. A yeast one-hybrid assay confirmed the direct interaction between SlERF.J2 and the SlCPS promoter. Collectively, this study clarifies the important function of SlERF.J2 in regulating drought and salt stress tolerance in tomato, providing genetic resources for tomato breeding.

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