Genome-wide identification and expression profile analysis of the Ras superfamily genes in eastern honeybee (Apis cerana)

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Comparative Biochemistry and Physiology D-Genomics & Proteomics Pub Date : 2025-02-20 DOI:10.1016/j.cbd.2025.101447
Dufu Li , Jun Zhang , Siming Liu , Yubo He , Qiang Ma , Pengfei Wang , Zhengang Ma , Jinshan Xu , Zeyang Zhou
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Abstract

The Ras superfamily, a crucial gene family in eukaryotes, functions as molecular switches that regulate various physiological and biochemical processes within cells. However, research on this topic remains limited concerning Apis cerana, a pollinator of significant economic and ecological importance. Here, 83 Ras superfamily genes in the genome of A. cerana were identified and classified into five distinct families. Phylogenetic analysis revealed that the homologous genes from two closely related species, A. cerana and Apis mellifera, clustered with relatively high bootstrap values. Notably, Rerg was unique to A. cerana compared to A. mellifera and had undergone gene duplication events. Expression profiles indicated diverse expression patterns of the Ras superfamily in the fat body during the holometabolous development of A. cerana. Most genes exhibited high expression levels during the later stages of adipose tissue remodeling; however, a minority were predominantly expressed during the prepupal (PP) and 1-day-old pupae (P1) stages. Among the 8 pairs of genes that had undergone gene duplication, 4 had inconsistent patterns, and 3 pairs were from the Ras family. In particular, Di-Ras2-2 was found to be highly expressed exclusively at the PP, and Rap2a-2 was only highly expressed during newly emerged (Em) stage. The observed differences in expression patterns may reflect adaptations to varying energy metabolism modes or environmental pressures. These findings provided a foundational basis for further investigation into the potential physiological roles of the Ras superfamily in A. cerana and offered valuable insights for analyzing this gene family across other insect species.

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Ras 超家族是真核生物中的一个重要基因家族,其功能是调节细胞内各种生理和生化过程的分子开关。然而,对于具有重要经济和生态意义的授粉昆虫--陶瓷蜜蜂(Apis cerana)来说,这方面的研究仍然有限。在此,我们鉴定了陶瓷蜂基因组中的 83 个 Ras 超家族基因,并将其分为五个不同的家族。系统进化分析表明,来自两个密切相关物种(A. cerana 和 Apis mellifera)的同源基因以相对较高的引导值聚类。值得注意的是,与 A. mellifera 相比,Rerg 是 A. cerana 独有的基因,并且经历了基因复制事件。表达图谱显示,Ras 超家族在鸟类全代谢发育过程中脂肪体中的表达模式多种多样。大多数基因在脂肪组织重塑的后期阶段表现出较高的表达水平;但也有少数基因在蛹前期(PP)和1日龄蛹(P1)阶段主要表达。在经历基因复制的 8 对基因中,有 4 对基因的表达模式不一致,其中 3 对来自 Ras 家族。其中,Di-Ras2-2只在PP阶段高表达,而Rap2a-2只在刚出生(Em)阶段高表达。观察到的表达模式差异可能反映了对不同能量代谢模式或环境压力的适应。这些发现为进一步研究 Ras 超家族在 Cerana 中的潜在生理作用提供了基础,并为分析该基因家族在其他昆虫物种中的作用提供了宝贵的见解。
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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