Department of Biological Sciences, University of North Carolina at Charlotte, Charlotte, North Carolina, USA.
Temple University, Philadelphia, PA, USA.
RNA Biol. 2021 Dec;18(12):2480-2497. doi: 10.1080/15476286.2021.1926747. Epub 2021 Jun 23.
is a deadly human pathogen responsible for the devastating disease called malaria. In this study, we measured the differential accumulation of RNA secondary structures in coding and non-coding transcripts from the asexual developmental cycle in in human red blood cells. Our comprehensive analysis that combined high-throughput nuclease mapping of RNA structures by duplex RNA-seq, SHAPE-directed RNA structure validation, immunoaffinity purification and characterization of antisense RNAs collectively measured differentially base-paired RNA regions throughout the parasite's asexual RBC cycle. Our mapping data not only aligned to a diverse pool of RNAs with known structures but also enabled us to identify new structural RNA regions in the malaria genome. On average, approximately 71% of the genes with secondary structures are found to be protein coding mRNAs. The mapping pattern of these base-paired RNAs corresponded to all regions of mRNAs, including the 5' UTR, CDS and 3' UTR as well as the start and stop codons. Histone family genes which are known to form secondary structures in their mRNAs and transcripts from genes which are important for transcriptional and post-transcriptional control, such as the unique plant-like transcription factor family, , DNA-/RNA-binding protein, and proteins important for RBC invasion and malaria cytoadherence also showed strong accumulation of duplex RNA reads in various asexual stages in . Intriguingly, our study determined stage-specific, dynamic relationships between mRNA structural contents and translation efficiency in asexual blood stages, suggesting an essential role of RNA structural changes in malaria gene expression programs. : CDS: Coding Sequence; DNA: Deoxyribonucleic Acid; dsRNA: double-stranded RNA; IDC: Intra-erythrocytic Developmental Cycle (IDC); m6A: N6-methyladenosine; mRNA: Messenger RNA; ncRNA: Non-coding RNA; RBC: Red Blood cells; RBP: RNA-Binding Protein; REC: Relative Expression Counts; RNA-seq: RNA-sequencing; RNA: Ribonucleic Acid; RNP: Ribonucleoprotein; RPKM: Reads Per Kilobase of transcript Per Million; rRNA: Ribosomal RNA 16. RUFs: RNAs of Unknown Function; SHAPE: Selective 2'-hydroxyl acylation analysed by primer extension; snoRNA: Small Nucleolar RNA; snRNA: Small Nuclear RNA; SRP-RNA: Signal Recognition Particle RNA; ssRNA: (Single-stranded RNA); TE: Translation Efficiency; tRNA: transfer RNA; UTR: Untranslated Region.
疟原虫是一种致命的人类病原体,可导致疟疾这种毁灭性疾病。在这项研究中,我们测量了疟原虫在人类红细胞无性发育周期中编码和非编码转录物中 RNA 二级结构的差异积累。我们的综合分析结合了高吞吐量核酸酶 RNA 结构的映射,通过双链 RNA-seq,形状指导的 RNA 结构验证,免疫亲和纯化和反义 RNA 的特征,共同测量了寄生虫无性 RBC 周期中整个寄生虫的差异碱基配对 RNA 区域。我们的映射数据不仅与具有已知结构的各种 RNA 库对齐,而且还使我们能够在疟原虫基因组中识别新的结构 RNA 区域。平均而言,约 71%具有二级结构的基因被发现是编码蛋白的 mRNA。这些碱基配对 RNA 的映射模式与 mRNA 的所有区域相对应,包括 5'UTR、CDS 和 3'UTR 以及起始和终止密码子。组蛋白家族基因在其 mRNA 中形成二级结构,而对于转录和转录后控制很重要的基因的转录物,例如独特的类植物转录因子家族、、DNA-/RNA 结合蛋白和对 RBC 入侵和疟疾细胞黏附很重要的蛋白质,也在 中的各种无性阶段中强烈积累双链 RNA 读数。有趣的是,我们的研究确定了疟原虫无性血阶段中 mRNA 结构含量与翻译效率之间的阶段特异性动态关系,表明 RNA 结构变化在疟原虫基因表达程序中起着重要作用。