紫花苜蓿MsWRKY47基因的克隆及耐盐功能分析
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国家自然科学基金项目(32201456,32071877)


Cloning and functional analysis of MsWRKY47 gene in alfalfa under salt stress
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    摘要:

    为明确紫花苜蓿(Medicago sativa) MsWRKY47基因在调节植物耐盐性中的作用,本研究以紫花苜蓿‘WL363 HQ’的cDNA为模板,克隆了MsWRKY47基因,并对其蛋白序列特征以及MsWRKY47转基因拟南芥的耐盐性进行了分析。结果表明:MsWRKY47编码区全长1 287 bp,编码428个氨基酸,含有一个WRKYGQK结构域,属于WRKY家族,与蒺藜苜蓿中同源蛋白MtWRKY47的亲缘关系最近;该基因在紫花苜蓿根中的表达量最高,且盐胁迫可诱导其表达;MsWRKY47蛋白定位于细胞核,不具备转录激活活性。盐胁迫后MsWRKY47转基因植株黄叶率高于野生型的黄叶率,氧化损伤程度更严重,表明MsWRKY47基因过表达降低了拟南芥的耐盐性,MsWRKY蛋白可能在植物对盐胁迫的响应过程中发挥负调控作用。

    Abstract:

    In order to clarify the role of MsWRKY47 gene of alfalfa(Medicago sativa) in regulating salt tolerance in plants, the MsWRKY47 gene was cloned using the cDNA of Medicago sativa ‘WL363 HQ’ as a template, and its protein sequence characteristics and the salt tolerance of MsWRKY47 transgenic Arabidopsis thaliana were analyzed. The results showed that the full length of MsWRKY47 coding region was 1 287 bp, which encoded 428 amino acids and contained a WRKYGQK domain, which belonged to WRKY family and was closely related to homologous protein MtWRKY47 in Medicago truncatula. The expression of MsWRKY47 was the highest in alfalfa roots and could be induced by salt stress. MsWRKY47 was localized in nucleus and had no transcriptional activation activity. The yellow leaf rate of transgenic plants was higher than that of wild type after salt stress, and the oxidative damage was more serious, indicating that the overexpression of MsWRKY47 gene reduced the salt tolerance of Arabidopsis. MsWRKY protein may play a negative regulatory role in the response of plants to salt stress.

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严帅凤,赵梦冉,徐倩,卢蕊,胡龙兴*.紫花苜蓿MsWRKY47基因的克隆及耐盐功能分析[J].湖南农业大学学报(自然科学版),2025,51(4):38-47.

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  • 在线发布日期: 2025-09-29
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