Desmodium styracifolium 的 DsWRKY6 基因的克隆和功能验证。

Plant signaling & behavior Pub Date : 2024-12-31 Epub Date: 2024-05-14 DOI:10.1080/15592324.2024.2349868
Qilin Yang, Jinheng Huang, Xiaofeng Nie, XiaoMin Tang, Peiran Liao, Quan Yang
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引用次数: 0

摘要

本研究旨在分析转录因子在Desmodium styracifolium中的作用,证明DsWRKY6转录因子与Desmodium styracifolium - cv. 'GuangYaoDa1'的植株表型有关,可用于分子辅助育种。以'广药大1号'为材料,以其DNA为模板克隆DsWRKY6,通过农杆菌介导的转化构建转基因拟南芥品系。对转基因拟南芥进行了表型和生理生化指标的研究。表型观察结果表明,与对照组相比,DsWRKY6转基因拟南芥的生长速度更快,主茎、茎叶侧枝和根的长度更长,但茎叶和茎叶侧枝的数量较少。这也表明它们的花期和果期都提前了。生理生化指标结果表明,与对照组相比,DsWRKY6转基因拟南芥中DsWRKY6的相对表达量增加,赤霉酸含量显著增加。根据上述结果,DsWRKY6能调控脱落酸含量提高引起的花果期提前,DsWRKY6转录因子的表达可能是'广药大1号'直立生长的原因。
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Cloning and functional validation of DsWRKY6 gene from Desmodium styracifolium.

The purpose of this study was to analyze the role of transcription factor in Desmodium styracifolium, proving that the DsWRKY6 transcription factor was related to the plant phenotypes of Desmodium styracifolium - cv. 'GuangYaoDa1' and it could be used in molecular-assisted breeding. 'GuangYaoDa1' was used as the material and its DNA was the template to clone DsWRKY6, the transgenic Arabidopsis thaliana line was constructed by agrobacterium tumefaciens‑mediated transformation. Transgenic Arabidopsis thaliana was cultivated to study phenotype and physiological and biochemical indexes. Phenotypic observation showed that DsWRKY6 transgenic Arabidopsis thaliana had a faster growth rate while compared with the control group, they had longer lengths of main stem, lateral branches of cauline leaves, and root, but a lower number of cauline leaves and lateral branches of cauline leaves. And it also showed that their flowering and fruiting periods were advanced. The results of physiological and biochemical indexes showed that the relative expressions of DsWRKY6 increased and the abscisic acid content significantly increased in DsWRKY6 transgenic Arabidopsis thaliana compared with the control group. According to the above results, DsWRKY6 could regulate the advancing of flowering and fruiting periods caused by the improvement of abscisic acid content, and expression of the DsWRKY6 transcription factor might be the cause of the upright growth of 'GuangYaoDa1'.

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