Smoniewski Clara M, Borujeni Poorya Mirzavand, Petersen Austin, Hampton Marshall, Salavati Reza, Zimmer Sara L
Department of Biomedical Sciences, University of Minnesota Medical School Duluth Campus, Duluth, MN, USA.
Institute of Parasitology, McGill University, Quebec, Canada.
bioRxiv. 2023 Feb 10:2023.02.10.528059. doi: 10.1101/2023.02.10.528059.
Since the first identification of circular RNA (circRNA) in viral-like systems, reports of circRNAs and their functions in various organisms, cell types, and organelles have greatly expanded. Here, we report the first evidence of circular mRNA in the mitochondrion of the eukaryotic parasite, . While using a circular RT-PCR technique developed to sequence mRNA tails of mitochondrial transcripts, we found that some mRNAs are circularized without an circularization step normally required to produce PCR products. Starting from total circularized RNA and circRNA, we high-throughput sequenced three transcripts from the 3' end of the coding region, through the 3' tail, to the 5' start of the coding region. We found that fewer reads in the circRNA libraries contained tails than in the total RNA libraries. When tails were present on circRNAs, they were shorter and less adenine-rich than the total population of RNA tails of the same transcript. Additionally, using hidden Markov modelling we determined that enzymatic activity during tail addition is different for circRNAs than for total RNA. Lastly, circRNA UTRs tended to be shorter and more variable than those of the same transcript sequenced from total RNA. We propose a revised model of Trypanosome mitochondrial tail addition, in which a fraction of mRNAs is circularized prior to the addition of adenine-rich tails and may act as a new regulatory molecule or in a degradation pathway.
自从在病毒样系统中首次鉴定出环状RNA(circRNA)以来,关于circRNA及其在各种生物体、细胞类型和细胞器中的功能的报道已大幅增加。在此,我们报告了真核寄生虫线粒体中环状mRNA的首个证据。在使用为对线粒体转录本的mRNA尾巴进行测序而开发的环状逆转录聚合酶链式反应(RT-PCR)技术时,我们发现一些mRNA被环化,而无需通常产生PCR产物所需的环化步骤。从总的环化RNA和circRNA开始,我们对编码区3'端的三个转录本进行了高通量测序,从3'尾巴一直到编码区的5'起始端。我们发现,circRNA文库中包含尾巴的读数比总RNA文库中的少。当circRNA上存在尾巴时,它们比同一转录本的RNA尾巴总数更短且富含腺嘌呤的程度更低。此外,使用隐马尔可夫模型,我们确定circRNA在尾巴添加过程中的酶活性与总RNA不同。最后,circRNA的非翻译区(UTR)往往比从总RNA测序得到的同一转录本的UTR更短且更具变异性。我们提出了一种经修订的锥虫线粒体尾巴添加模型,其中一部分mRNA在添加富含腺嘌呤的尾巴之前被环化,并且可能作为一种新的调节分子或参与降解途径。