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海滨牵牛中WRKY转录因子的鉴定及IpWRKY16在甘薯盐胁迫响应中的功能作用

Identification of WRKY transcription factors in Ipomoea pes-caprae and functional role of IpWRKY16 in sweet potato salt stress response.

作者信息

Wu Jiaying, Su Yiren, Pan Zhiyuan, Wang Yiming, Zhang Yongjing, Li Ludan, Jiang Jihong, Cao Xiaoying

机构信息

The Key Laboratory of Biotechnology for Medicinal and Edible Plants of Jiangsu Province, School of Life Science, Jiangsu Normal University, Xuzhou, Jiangsu, 221116, China.

出版信息

BMC Plant Biol. 2024 Dec 19;24(1):1190. doi: 10.1186/s12870-024-05928-2.

Abstract

BACKGROUND

WRKY transcription factors are plant-specific and play essential roles in growth, development, and stress responses, including reactions to salt, drought, and cold. Despite their significance, the WRKY genes in the wild sweet potato ancestor, Ipomoea pes-caprae, remain unexplored.

RESULTS

In this study, 65 WRKY genes were identified in the I. pes-caprae transcriptomic data. A phylogenetic tree incorporating Arabidopsis thaliana and Ipomoea batatas revealed seven major groups, each characterized by conserved gene structural features. Transcriptome data of I. pes-caprae under salt stress conditions identified 17 highly expressed WRKY genes, whose promoter regions contain cis-acting elements associated with plant growth, stress responses, and hormone signaling. Further analysis revealed that the 17 IpWRKY genes exhibited differential expression patterns under various abiotic stresses, suggesting their potential roles in specific stress responses. The gene IpWRKY16 was significantly up-expressed under salt stress, drought, salicylic acid (SA), and abscisic acid (ABA) treatments. Subcellular localization analysis confirmed that IpWRKY16 is located in the nucleus. Under salt stress, IpWRKY16 overexpressing roots showed high activity in superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and low content in malondialdehyde (MDA). Using non-invasive micro-test technology (NMT), a significant efflux of Na was observed in the elongation zones of sweet potato adventitious roots that overexpressed IpWRKY16. Quantitative reverse transcription PCR (qRT-PCR) revealed that several ion transporter genes were responsive to IpWRKY16 expression, with IbSOS3, IbAHA4-1, and IbAHA4-2 showing the highest expression levels. We hypothesize that IpWRKY16 responds to salt stress by forming a complex regulatory network involving these key genes.

CONCLUSIONS

This study provides a foundational understanding of WRKY transcription factors in I. pes-caprae, offering insights into their potential role in enhancing salt-tolerance in sweet potato. Our findings contribute valuable genetic knowledge that could aid in the molecular breeding of stress-resilient sweet potato varieties.

摘要

背景

WRKY转录因子是植物特有的,在生长、发育和胁迫响应(包括对盐、干旱和寒冷的反应)中发挥着重要作用。尽管它们很重要,但野生甘薯祖先厚藤中的WRKY基因仍未被探索。

结果

在本研究中,从厚藤转录组数据中鉴定出65个WRKY基因。结合拟南芥和甘薯的系统发育树显示有七个主要类群,每个类群都具有保守的基因结构特征。厚藤在盐胁迫条件下的转录组数据确定了17个高表达的WRKY基因,其启动子区域含有与植物生长、胁迫响应和激素信号传导相关的顺式作用元件。进一步分析表明,这17个厚藤WRKY基因在各种非生物胁迫下表现出不同的表达模式,表明它们在特定胁迫响应中的潜在作用。基因IpWRKY16在盐胁迫、干旱、水杨酸(SA)和脱落酸(ABA)处理下显著上调表达。亚细胞定位分析证实IpWRKY16位于细胞核中。在盐胁迫下,过表达IpWRKY16的根中超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)活性高,丙二醛(MDA)含量低。使用非损伤微测技术(NMT),在过表达IpWRKY16的甘薯不定根伸长区观察到大量的Na外流。定量逆转录PCR(qRT-PCR)显示,几个离子转运基因对IpWRKY16的表达有响应,其中IbSOS3、IbAHA4-1和IbAHA4-2的表达水平最高。我们假设IpWRKY16通过形成一个涉及这些关键基因的复杂调控网络来响应盐胁迫。

结论

本研究为厚藤中WRKY转录因子提供了基础认识,深入了解了它们在增强甘薯耐盐性方面的潜在作用。我们的研究结果提供了有价值的遗传知识,有助于抗逆甘薯品种的分子育种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5c6/11656888/bcb9fc11f676/12870_2024_5928_Fig1_HTML.jpg

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