中国农业科学 ›› 2026, Vol. 59 ›› Issue (4): 793-806.doi: 10.3864/j.issn.0578-1752.2026.04.007

• 植物保护 • 上一篇    下一篇

烟粉虱MED脂肪酸延长酶基因家族鉴定和表达分析

江峰1(), 吴春燕1, 王亦好1, 杨泽众2, 龚成1(), 罗晨1   

  1. 1 扬州大学植物保护学院, 江苏扬州 225000
    2 天津市农业科学院植物保护研究所, 天津 300381
  • 收稿日期:2025-11-15 出版日期:2026-02-10 发布日期:2026-02-10
  • 通信作者:
    龚成,E-mail:
  • 联系方式: 江峰,E-mail:jiangfeng23333@163.com。
  • 基金资助:
    江苏省自然科学基金(BK20250896); 国家自然科学基金(32502467); 天津市自然科学基金(24JCYBJC00880)

Identification and Expression Analysis of the Fatty Acid Elongase Gene Family in Bemisia tabaci MED

JIANG Feng1(), WU ChunYan1, WANG YiHao1, YANG ZeZhong2, GONG Cheng1(), LUO Chen1   

  1. 1 College of Plant Protection, Yangzhou University, Yangzhou 225000, Jiangsu
    2 Institute of Plant Protection, Tianjin Academy of Agricultural Sciences, Tianjin 300381
  • Received:2025-11-15 Published:2026-02-10 Online:2026-02-10

摘要:

【目的】烟粉虱(Bemisia tabaci)的宿主适应性与其脂类物质代谢(特别是脂肪酸代谢)的可塑性密切相关。脂肪酸延长酶(fatty acid elongase,ELO)为脂肪酸代谢网络的核心调控因子,系统解析其基因家族,揭示烟粉虱营养适应与繁殖发育的代谢调控机制,为害虫绿色防控机制提供新型靶标基因资源。【方法】基于烟粉虱MED基因组和其他昆虫的ELO基因序列,通过多重序列比对,鉴定烟粉虱ELO,采用RT-PCR扩增并克隆获得22条BtELO基因序列。利用生物信息学工具系统分析其基因结构、蛋白理化性质,利用最大似然法构建BtELO与其他半翅目昆虫ELO的系统进化树。通过实时荧光定量PCR(qRT-PCR)方法检测BtELO在烟粉虱不同发育阶段(卵、1—4龄若虫、成虫)及成虫不同组织(头、胸、腹)中的时空表达谱。【结果】成功鉴定并克隆得到22条BtELO基因CDS序列,长度为714—1 296 bp,分布在烟粉虱MED基因组10条SCAFFOLD上,按照线性排列顺序依次命名为BtELO1—22,编码237—431个氨基酸,蛋白整体呈现出疏水性,含有6—7个跨膜结构域,亚细胞定位分析预测均在内质网中;氨基酸序列比对和系统进化分析显示,BtELO蛋白具有典型的ELO保守结构域和组氨酸簇(HXXHH),BtELO基因家族内部成员相似度最高达到76%,BtELO可分为7大进化分支,并呈现出较好的系统发育聚类特征,进化关系保守,部分BtELO形成相对独立分支,存在基因复制事件;时空表达谱分析显示,BtELO在烟粉虱的不同发育阶段和组织中的表达具有明显时空特异性,表明BtELO在烟粉虱中可能发挥着多种功能。【结论】烟粉虱22条BtELO含有典型的延长酶结构域及HXXHH保守基序,其在烟粉虱不同发育阶段和组织中均有表达,部分基因在卵期和成虫腹部高表达,推测其在生殖过程中发挥作用,而在若虫期高表达的基因可能与生长发育及蜕皮相关。

关键词: 烟粉虱, 脂肪酸延长酶, 基因家族, 生物信息学, 实时荧光定量PCR

Abstract:

【Objective】The host adaptability of Bemisia tabaci is closely associated with the plasticity of its lipid metabolism, particularly fatty acid metabolism. Fatty acid elongases (ELOs) are key regulatory components in fatty acid biosynthesis and modification. A comprehensive characterization of the ELO gene family in B. tabaci will contribute to elucidate the metabolic mechanisms underlying its nutritional adaptation, growth, and reproduction, and to identify novel target gene resources for sustainable green pest management strategies.【Method】Based on the B. tabaci MED genome and ELO sequences from other insects, ELO genes in B. tabaci were identified through multiple sequence alignment, 22 BtELO coding sequences were amplified and cloned using RT-PCR. Bioinformatics analyses were conducted to determine gene structure and protein physicochemical properties, and a maximum-likelihood phylogenetic tree was constructed to examine the evolutionary relationships between BtELOs and ELO genes from other Hemipteran insects. The temporal and spatial expression patterns of BtELOs in different developmental stages (egg, 1st-4th instar nymphs, and adults) and in various adult tissues (head, thorax, and abdomen) were analyzed using quantitative real-time PCR (qRT-PCR).【Result】A total of 22 BtELOs CDS were successfully identified and cloned, ranging from 714 to 1 296 bp. These genes, located on 10 genomic SCAFFOLDs, were sequentially designated BtELO1 through BtELO22 based on their linear arrangement. The encoded proteins, comprising 237 to 431 amino acids, are generally hydrophobic, contain 6-7 transmembrane domains, and are predicted to localize in the endoplasmic reticulum. Sequence alignment and phylogenetic analyses revealed that BtELO proteins possess the typical ELO conserved domain and histidine cluster (HXXHH). The sequence similarity among BtELO family members was as high as 76%. The BtELOs were grouped into 7 major evolutionary clades with clear phylogenetic clustering patterns, indicating conserved evolutionary relationships, with some genes forming independent clades indicative of gene duplication events. Spatiotemporal expression profiling revealed that the expression of BtELOs exhibited clear stage- and tissue-specific patterns in B. tabaci, indicating that these genes may perform diverse biological functions in this species.【Conclusion】The 22 BtELOs identified in B. tabaci contain the typical elongase domain and the conserved HXXHH motif. All BtELOs are expressed in various developmental stages and tissues of B. tabaci. Several genes exhibit high expression in eggs and adult abdomens, suggesting potential roles in reproductive processes, whereas those highly expressed during the nymphal stages may be associated with growth, development, and molting.

Key words: Bemisia tabaci, fatty acid elongase (ELO), gene family, bioinformatics, qRT-PCR