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首页> 外文期刊>BMC Genomics >Integrating microRNA and mRNA expression profiling in Symbiodinium microadriaticum, a dinoflagellate symbiont of reef-building corals
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Integrating microRNA and mRNA expression profiling in Symbiodinium microadriaticum, a dinoflagellate symbiont of reef-building corals

机译:整合微小RNA和mRNA表达谱的Symbiodinium microadriaticum,一种造礁珊瑚的鞭毛共生体

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Background Animal and plant genomes produce numerous small RNAs (smRNAs) that regulate gene expression post-transcriptionally affecting metabolism, development, and epigenetic inheritance. In order to characterize the repertoire of endogenous smRNAs and potential gene targets in dinoflagellates, we conducted smRNA and mRNA expression profiling over 9 experimental treatments of cultures from Symbiodinium microadriaticum, a photosynthetic symbiont of scleractinian corals. Results We identified a set of 21 novel smRNAs that share stringent key features with functional microRNAs from other model organisms. smRNAs were predicted independently over all 9 treatments and their putative gene targets were identified. We found 1,720 animal-like target sites in the 3'UTRs of 12,858 mRNAs and 19 plant-like target sites in 51,917 genes. We assembled a transcriptome of 58,649 genes and determined differentially expressed genes (DEGs) between treatments. Heat stress was found to produce a much larger number of DEGs than other treatments that yielded only few DEGs. Analysis of DEGs also revealed that minicircle-encoded photosynthesis proteins seem to be common targets of transcriptional regulation. Furthermore, we identified the core RNAi protein machinery in Symbiodinium. Conclusions Integration of smRNA and mRNA expression profiling identified a variety of processes that could be under microRNA control, e.g. protein modification, signaling, gene expression, and response to DNA damage. Given that Symbiodinium seems to have a paucity of transcription factors and differentially expressed genes, identification and characterization of its smRNA repertoire establishes the possibility of a range of gene regulatory mechanisms in dinoflagellates acting post-transcriptionally.
机译:背景动植物基因组产生大量的小RNA(smRNA),它们在转录后调节基因表达,从而影响代谢,发育和表观遗传。为了表征在鞭毛藻中内源性smRNA和潜在基因靶标的组成,我们对9种来自巩膜珊瑚的光合共生体的微生物Symbiodinium microadriaticum的培养物进行了9种实验处理,进行了smRNA和mRNA表达谱分析。结果我们鉴定出一组21种与其他模型生物的功能性microRNA具有严格关键特征的新颖smRNA。在所有9种治疗方法中均独立预测了smRNA,并确定了其推定的基因靶标。我们在12,858个mRNA的3'UTR中发现了1,720个动物样靶位,在51,917个基因中发现了19个植物样靶位。我们组装了58,649个基因的转录组,并确定了治疗之间的差异表达基因(DEG)。发现热应力比仅产生少量DEG的其他处理产生更多数量的DEG。对DEG的分析还显示,微环编码的光合作用蛋白似乎是转录调控的常见靶标。此外,我们确定了Symbiodinium中的核心RNAi蛋白机制。结论smRNA和mRNA表达谱的整合确定了microRNA控制下的多种过程,例如蛋白质修饰,信号传导,基因表达以及对DNA损伤的反应。鉴于Symbiodinium似乎缺乏转录因子和差异表达的基因,其smRNA组成库的鉴定和表征确定了在鞭毛鞭毛虫中转录后起作用的一系列基因调控机制的可能性。

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