College of Animal Sciences (College of Bee Science), Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Apitherapy Research Institute of Fujian Province, Fuzhou 350002, China.
Int J Mol Sci. 2023 Oct 20;24(20):15399. doi: 10.3390/ijms242015399.
Long non-coding RNAs (lncRNAs) are crucial modulators in a variety of biological processes, such as gene expression, development, and immune defense. However, little is known about the function of lncRNAs in the development of Asian honey bee () larval guts. Here, on the basis of our previously obtained deep-sequencing data from the 4-, 5-, and 6-day-old larval guts of workers (Ac4, Ac5, and Ac6 groups), an in-depth transcriptome-wide investigation was conducted to decipher the expression pattern, regulatory manners, and potential roles of lncRNAs during the developmental process of worker larval guts, followed by the verification of the relative expression of differentially expressed lncRNAs (DElncRNAs) and the targeting relationships within a competing endogenous RNA (ceRNA) axis. In the Ac4 vs. Ac5 and Ac5 vs. Ac6 comparison groups, 527 and 498 DElncRNAs were identified, respectively, which is suggestive of the dynamic expression of lncRNAs during the developmental process of larval guts. A -acting analysis showed that 330 and 393 neighboring genes of the aforementioned DElncRNAs were respectively involved in 29 and 32 functional terms, such as cellular processes and metabolic processes; these neighboring genes were also respectively engaged in 246 and 246 pathways such as the Hedgehog signaling pathway and the Wnt signaling pathway. Additionally, it was found that 79 and 76 DElncRNAs as potential antisense lncRNAs may, respectively, interact with 72 and 60 sense-strand mRNAs. An investigation of competing endogenous RNA (ceRNA) networks suggested that 75 (155) DElncRNAs in the Ac4 vs. Ac5 (Ac5 vs. Ac6) comparison group could target 7 (5) DEmiRNAs and further bind to 334 (248) DEmRNAs, which can be annotated to 33 (29) functional terms and 186 (210) pathways, including 12 (16) cellular- and humoral-immune pathways (lysosome pathway, necroptosis, MAPK signaling pathway, etc.) and 11 (10) development-associated signaling pathways (Wnt, Hippo, AMPK, etc.). The RT-qPCR detection of five randomly selected DElncRNAs confirmed the reliability of the used sequencing data. Moreover, the results of a dual-luciferase reporter assay were indicative of the binding relationship between MSTRG.11294.1 and miR-6001-y and between miR-6001-y and ncbi_107992440. These results demonstrate that DElncRNAs are likely to modulate the developmental process of larval guts via the regulation of the source genes' transcription, interaction with mRNAs, and ceRNA networks. Our findings not only yield new insights into the developmental mechanism underlying larval guts, but also provide a candidate ceRNA axis for further functional dissection.
长链非编码 RNA(lncRNA)是多种生物学过程(如基因表达、发育和免疫防御)中的关键调节因子。然而,人们对 lncRNA 在亚洲蜜蜂()幼虫肠道发育中的功能知之甚少。在这里,我们基于之前从工蜂 4 日龄(Ac4)、5 日龄(Ac5)和 6 日龄(Ac6)幼虫肠道获得的深度测序数据,对 lncRNA 在工蜂幼虫肠道发育过程中的表达模式、调控方式和潜在作用进行了深入的全转录组研究,随后对差异表达 lncRNA(DElncRNA)的相对表达和竞争内源性 RNA(ceRNA)轴内的靶向关系进行了验证。在 Ac4 与 Ac5 和 Ac5 与 Ac6 的比较组中,分别鉴定出 527 和 498 个 DElncRNA,表明 lncRNA 在幼虫肠道发育过程中存在动态表达。A- 活性分析表明,上述 DElncRNA 的 330 和 393 个邻近基因分别参与了 29 和 32 个功能术语,如细胞过程和代谢过程;这些邻近基因还分别参与了 246 和 246 条途径,如 Hedgehog 信号通路和 Wnt 信号通路。此外,还发现 79 和 76 个作为潜在反义 lncRNA 的 DElncRNA 可能分别与 72 和 60 个有义链 mRNA 相互作用。ceRNA 网络的研究表明,在 Ac4 与 Ac5(Ac5 与 Ac6)比较组中,75(155)个 DElncRNA 可以靶向 7(5)个 DEmiRNA,并进一步与 334(248)个 DEmRNA 结合,这些 DEmRNA 可以被注释为 33(29)个功能术语和 186(210)个途径,包括 12(16)个细胞和体液免疫途径(溶酶体途径、坏死性凋亡、MAPK 信号通路等)和 11(10)个发育相关信号通路(Wnt、Hippo、AMPK 等)。对五个随机选择的 DElncRNA 的 RT-qPCR 检测证实了所使用测序数据的可靠性。此外,双荧光素酶报告基因检测结果表明,MSTRG.11294.1 和 miR-6001-y 之间以及 miR-6001-y 和 ncbi_107992440 之间存在结合关系。这些结果表明,DElncRNA 可能通过调节源基因的转录、与 mRNAs 的相互作用和 ceRNA 网络来调节幼虫肠道的发育过程。我们的研究结果不仅为蜜蜂幼虫肠道的发育机制提供了新的见解,而且为进一步的功能分析提供了候选 ceRNA 轴。