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生态学杂志 ›› 2026, Vol. 45 ›› Issue (9): 2894-2901.

• ·红树林湿地生态学专栏·(专栏组织专家:曹文志、王文卿、宋长春) • 上一篇    下一篇

濒危红树小花老鼠簕AeFLA17基因时空表达模式及其参与非生物胁迫响应特征

陈旭1,邓宝珍2,廖丽娴2,钟才荣1,程成1,张颖1,2*   

  1. 1海南省林业科学研究院(海南省红树林研究院), 海口 571129; 2岭南师范学院红树林珍稀濒危物种保护与利用工程技术研究中心, 广东湛江 524048)
  • 出版日期:2026-09-10 发布日期:2026-09-07

Spatiotemporal expression pattern and abiotic stress response characteristics of the AeFLA17 gene in the endangered mangrove Acanthus ebracteatus Vahl.

CHEN Xu1, DENG Baozhen2, LIAO Lixian2, ZHONG Cairong1, CHENG Cheng1, ZHANG Ying1,2*   

  1. (1Hainan Academy of Forestry (Hainan Academy of Mangrove), Haikou 571129, China; 2Engineering and Technological Research Center in Protection and Utilization of Mangrove Rare and Endangered Species, Lingnan Normal University, Zhanjiang 524048, Guangdong, China).

  • Online:2026-09-10 Published:2026-09-07

摘要:

类成束阿拉伯半乳糖蛋白(FLAs)在植物逆境生长发育中起重要作用,但在濒危红树植物小花老鼠簕(Acanthus ebracteatus)中FLAs是否参与其潮间带海水生境适应机制尚不清楚。本研究克隆了该红树植物AeFLA17基因并探究其在小花老鼠簕中的组织特异性表达及花发育过程中的时空表达,进一步分析小花老鼠簕在高温、低温、盐、干旱、水淹和镉等非生物胁迫下AeFLA17基因在叶片中的表达模式。结果表明,AeFLA17基因全长2194 bp,包含1410 bp的编码区(CDS),编码469个氨基酸,无内含子,为亲水性不稳定蛋白;系统进化分析表明,AeFLA17与爵床科中穿心莲FLA蛋白具有较近的亲缘关系。亚细胞定位发现,AeFLA17蛋白位于细胞质。实时荧光定量实验表明,AeFLA17基因在小花老鼠簕叶中的表达量最低,在花中表达量最高,且在盛花期表达量最高;在热胁迫下,12 h时AeFLA17表达显著上调,24 h后迅速下降,48 h时表达略有回升但未达到显著水平;在冷胁迫条件下,24 h及以后表达水平明显升高;镉胁迫处理48 h后表达量显著上调;相反,在干旱胁迫下,24 h与48 h均表现出明显抑制;水淹和盐胁迫下,随着胁迫时间的延长,基因表达呈现逐步降低趋势。上述结果表明,AeFLA17基因的表达动态揭示其参与了植物响应多胁迫应答网络,为进一步解析成束阿拉伯半乳糖蛋白家族的功能及抗逆分子育种提供了重要理论依据。


关键词: 小花老鼠簕, 类成束阿拉伯半乳糖蛋白(FLAs), 基因克隆, 非生物胁迫, 亚细胞定位

Abstract: Fasciclin-like arabinogalactan proteins (FLAs) play an important role in the growth and development of plants under stresses. However, it is unclear whether FLAs are involved in the adaptation mechanism of endangered mangrove species Acanthus ebracteatus in the intertidal marine habitat. In this study, we cloned the AeFLA17 gene from A. ebracteatus, investigated its tissuespecific expression across different organs and spatiotemporal expression patterns during floral development, and further analyzed its expression profiles in the leaves under various abiotic stresses, including high temperature, low temperature, salt, drought, waterlogging, and cadmium. The results showed that the AeFLA17 gene is 2194 bp in length, contains a complete coding sequence of 1410 bp, encoding 469 amino acids with no introns, and is a hydrophilic and unstable protein. Phylogenetic analysis indicated that AeFLA17 was closely related to the FLA protein of Andrographis paniculata in the family Acanthaceae. Subcellular localization revealed that the AeFLA17 protein was localized in the cytoplasm. Quantitative real-time PCR experiments indicated that the AeFLA17 gene showed the lowest expression level in the leaves and the highest in the flowers of A. ebracteatus, with peak expression observed during the full bloom stage. The expression of AeFLA17 was significantly upregulated at 12 h, but rapidly decreased after 24 h. It slightly recovered at 48 h but did not reach a significant level under heat stress. Under cold stress, the expression level increased significantly after 24 h and continued to increase. After 48 h of cadmium stress treatment, the expression level was significantly up-regulated. However, under drought stress, the expression level at both 24 and 48 h showed obvious inhibition. Under flooding stress and salt stress, the gene expression showed a gradual decrease trend with the extension of stress time. This dynamic expression of AeFLA17 reveals its role in the plant response network to multiple stresses, providing an important theoretical basis for further analysis of the function of the FLA protein family and molecular breeding for stress resistance.


Key words: Acanthus ebracteatus, fasciclin-like arabinogalactan proteins (FLAs), gene cloning, abiotic stress, subcellular localization