Regulatory roles of long non-coding RNAs in short-term heat stress in adult worker bees

被引:0
|
作者
Zhang, Bing [1 ]
Zhang, Chaoying [1 ]
Zhang, Jiangchao [1 ]
Lu, Surong [1 ]
Zhao, Huiting [2 ]
Jiang, Yusuo [1 ]
Ma, Weihua [3 ]
机构
[1] Shanxi Agr Univ, Coll Anim Sci, Jinzhong, Shanxi, Peoples R China
[2] Shanxi Agr Univ, Coll Life Sci, Jinzhong, Shanxi, Peoples R China
[3] Shanxi Agr Univ, Coll Hort, Taiyuan, Shanxi, Peoples R China
来源
BMC GENOMICS | 2024年 / 25卷 / 01期
关键词
Apis mellifera; Cis-regulation; Heat stress; lncRNA; MSTRG.9645.5; Network regulation; Trans-regulation; RESPONSES; REVEALS; SHOCK;
D O I
10.1186/s12864-024-10399-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Long non-coding RNAs (lncRNAs) are crucial modulators of post-transcriptional gene expression regulation, cell fate determination, and disease development. However, lncRNA functions during short-term heat stress in adult worker bees are poorly understood. Here, we performed deep sequencing and bioinformatic analyses of honeybee lncRNAs. RNA interference was performed by using siRNA targeting the most highly expressed lncRNA. The silencing effect on lncRNA and the relative expression levels of seven heat shock protein (HSP) genes, were subsequently examined. Overall, 7,842 lncRNAs and 115 differentially expressed lncRNAs (DELs) were identified in adult worker bees following heat stress exposure. Structural analysis revealed that the overall expression abundance, length of transcripts, exon number, and open reading frames of lncRNAs were lower than those of mRNAs. GO analysis revealed that the target genes were mainly involved in "metabolism," "protein folding," "response to stress," and "signal transduction" pathways. KEGG analysis indicated that the "protein processing in endoplasmic reticulum" and "longevity regulating pathway-multiple species" pathways were most enriched. Quantitative real-time polymerase chain reaction (qRT-PCR) detection of the selected DELs confirmed the reliability of the sequencing data. Moreover, the siRNA experiment indicated that feeding siRNA yielded a silencing efficiency of 77.51% for lncRNA MSTRG.9645.5. Upon silencing this lncRNA, the expression levels of three HSP genes were significantly downregulated (p < 0.05), whereas those of three other HSP genes were significantly upregulated (p < 0.05). Our results provide a new perspective for understanding the regulatory mechanisms of lncRNAs in adult worker bees under short-term heat stress.
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页数:13
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