Philips Anna, Nowis Katarzyna, Stelmaszczuk Michal, Jackowiak Paulina, Podkowiński Jan, Handschuh Luiza, Figlerowicz Marek
Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland.
Institute of Computing Science, Poznan University of Technology, Poznan, Poland.
Front Plant Sci. 2020 Sep 10;11:576581. doi: 10.3389/fpls.2020.576581. eCollection 2020.
RNA-seq is currently the only method that can provide a comprehensive landscape of circular RNA (circRNAs) in the whole organism and its particular organs. Recent years have brought an increasing number of RNA-seq-based reports on plant circRNAs. Notably, the picture they revealed is questionable and depends on the applied circRNA identification and quantification techniques. In consequence, little is known about the biogenesis and functions of circRNAs in plants. In this work, we tested two experimental and six bioinformatics procedures of circRNA analysis to determine the optimal approach for studying the profiles of circRNAs in . Then using the optimized strategy, we determined the accumulation of circular and corresponding linear transcripts in plant seedlings and organs. We observed that only a small fraction of circRNAs was reproducibly generated. Among them, two groups of circRNAs were discovered: ubiquitous and organ-specific. The highest number of circRNAs with significantly increased accumulation in comparison to other organs/seedlings was found in roots. The circRNAs in seedlings, leaves and flowers originated mainly from genes involved in photosynthesis and the response to stimulus. The levels of circular and linear transcripts were not correlated. Although RNase R treatment enriches the analyzed RNA samples in circular transcripts, it may also have a negative impact on the stability of some of the circRNAs. We also showed that the normalization of NGS data by the library size is not proper for circRNAs quantification. Alternatively, we proposed four other normalization types whose accuracy was confirmed by ddPCR. Moreover, we provided a comprehensive characterization of circRNAs in organs and in seedlings. Our analyses revealed that plant circRNAs are formed in both stochastic and controlled processes. The latter are less frequent and likely engage circRNA-specific mechanisms. Only a few circRNAs were organ-specific. The lack of correlation between the accumulation of linear and circular transcripts indicated that their biogenesis depends on different mechanisms.
RNA测序是目前唯一能够全面呈现整个生物体及其特定器官中环状RNA(circRNA)情况的方法。近年来,基于RNA测序的关于植物circRNA的报道越来越多。值得注意的是,他们所揭示的情况存在疑问,并且取决于所应用的circRNA鉴定和定量技术。因此,关于植物中circRNA的生物合成和功能知之甚少。在这项工作中,我们测试了两种circRNA分析的实验方法和六种生物信息学程序,以确定研究[具体植物名称未给出]中circRNA谱的最佳方法。然后使用优化后的策略,我们确定了植物幼苗和器官中环状转录本和相应线性转录本的积累情况。我们观察到只有一小部分circRNA是可重复产生的。其中,发现了两组circRNA:普遍存在的和器官特异性的。与其他器官/幼苗相比,根部中积累显著增加的circRNA数量最多。幼苗、叶片和花朵中的circRNA主要来源于参与光合作用和对刺激反应的基因。环状转录本和线性转录本的水平不相关。尽管RNase R处理能使分析的RNA样本中环状转录本富集,但它也可能对某些circRNA的稳定性产生负面影响。我们还表明,通过文库大小对NGS数据进行标准化不适用于circRNA定量。另外,我们提出了其他四种标准化类型,其准确性通过数字PCR得到了证实。此外,我们对[具体植物名称未给出]器官和幼苗中的circRNA进行了全面表征。我们的分析表明,植物circRNA是在随机和受控过程中形成的。后者发生频率较低,可能涉及circRNA特异性机制。只有少数circRNA是器官特异性的。线性转录本和环状转录本积累之间缺乏相关性表明它们的生物合成依赖于不同的机制。