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MicroRNA-34 直接靶向蜜蜂的配对规则基因和细胞骨架成分。

MicroRNA-34 directly targets pair-rule genes and cytoskeleton component in the honey bee.

机构信息

Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil.

Monash Institute for Cognitive and Clinical Neuroscience, Monash University, Melbourne, Australia.

出版信息

Sci Rep. 2017 Jan 18;7:40884. doi: 10.1038/srep40884.

Abstract

MicroRNAs (miRNAs) are key regulators of developmental processes, such as cell fate determination and differentiation. Previous studies showed Dicer knockdown in honeybee embryos disrupt the processing of functional mature miRNAs and impairs embryo patterning. Here we investigated the expression profiles of miRNAs in honeybee embryogenesis and the role of the highly conserved miR-34-5p in the regulation of genes involved in insect segmentation. A total of 221 miRNAs were expressed in honey bee embryogenesis among which 97 mature miRNA sequences have not been observed before. Interestingly, we observed a switch in dominance between the 5-prime and 3-prime arm of some miRNAs in different embryonic stages; however, most miRNAs present one dominant arm across all stages of embryogenesis. Our genome-wide analysis of putative miRNA-target networks and functional pathways indicates miR-34-5p is one of the most conserved and connected miRNAs associated with the regulation of genes involved in embryonic patterning and development. In addition, we experimentally validated that miR-34-5p directly interacts to regulatory elements in the 3'-untranslated regions of pair-rule (even-skipped, hairy, fushi-tarazu transcription factor 1) and cytoskeleton (actin5C) genes. Our study suggests that miR-34-5p may regulate the expression of pair-rule and cytoskeleton genes during early development and control insect segmentation.

摘要

微小 RNA(miRNAs)是发育过程的关键调节因子,如细胞命运决定和分化。先前的研究表明,在蜜蜂胚胎中敲低 Dicer 会破坏功能性成熟 miRNAs 的加工,并损害胚胎模式形成。在这里,我们研究了 miRNAs 在蜜蜂胚胎发生中的表达谱,以及高度保守的 miR-34-5p 在调节昆虫分节基因中的作用。在蜜蜂胚胎发生中,共表达了 221 种 miRNAs,其中 97 种成熟 miRNA 序列以前未观察到。有趣的是,我们观察到在不同胚胎阶段,一些 miRNAs 的 5' 端和 3' 端优势之间发生了转变;然而,大多数 miRNAs 在胚胎发生的所有阶段都表现出一个主要的臂。我们对假定的 miRNA 靶标网络和功能途径的全基因组分析表明,miR-34-5p 是与调节参与胚胎模式形成和发育的基因相关的最保守和连接的 miRNAs 之一。此外,我们通过实验验证了 miR-34-5p 直接与配对规则(even-skipped、hairy、fushi-tarazu 转录因子 1)和细胞骨架(actin5C)基因 3' 非翻译区的调节元件相互作用。我们的研究表明,miR-34-5p 可能在早期发育过程中调节配对规则和细胞骨架基因的表达,并控制昆虫的分节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e596/5241629/01a7e53eb6c9/srep40884-f1.jpg

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