Singapore-MIT Alliance for Research and Technology, Infectious Disease Interdisciplinary Research Group, Campus for Research Excellence and Technological Enterprise, Singapore 138602, Department of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Department of Biological Engineering and Center for Environmental Health Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA, Applied Biological Science Program, Chulabhorn Graduate Institute, Bangkok 10210, Thailand, Division of Molecular Genetics & Cell Biology, School of Biological Sciences, Nanyang Technological University, Singapore 637551, Immunology Programme, Life Science Institute, Centre for Life Science, Singapore 117456 and Novartis Institute for Tropical Disease, Singapore 138670.
Nucleic Acids Res. 2013 Sep;41(17):e168. doi: 10.1093/nar/gkt668. Epub 2013 Aug 1.
A renewed interest in non-coding RNA (ncRNA) has led to the discovery of novel RNA species and post-transcriptional ribonucleoside modifications, and an emerging appreciation for the role of ncRNA in RNA epigenetics. Although much can be learned by amplification-based analysis of ncRNA sequence and quantity, there is a significant need for direct analysis of RNA, which has led to numerous methods for purification of specific ncRNA molecules. However, no single method allows purification of the full range of cellular ncRNA species. To this end, we developed a multidimensional chromatographic platform to resolve, isolate and quantify all canonical ncRNAs in a single sample of cells or tissue, as well as novel ncRNA species. The applicability of the platform is demonstrated in analyses of ncRNA from bacteria, human cells and plasmodium-infected reticulocytes, as well as a viral RNA genome. Among the many potential applications of this platform are a system-level analysis of the dozens of modified ribonucleosides in ncRNA, characterization of novel long ncRNA species, enhanced detection of rare transcript variants and analysis of viral genomes.
对非编码 RNA(ncRNA)的重新关注导致了新型 RNA 种类和转录后核糖核苷修饰的发现,并对 ncRNA 在 RNA 表观遗传学中的作用有了新的认识。虽然通过扩增分析 ncRNA 的序列和数量可以了解很多信息,但直接分析 RNA 的需求也非常迫切,这导致了许多特定 ncRNA 分子的纯化方法的出现。然而,没有一种单一的方法可以纯化所有细胞 ncRNA 种类。为此,我们开发了一种多维色谱平台,可以在单个细胞或组织样本中解析、分离和定量所有典型的 ncRNA,以及新型 ncRNA。该平台在细菌、人类细胞和疟原虫感染的网织红细胞以及病毒 RNA 基因组中的 ncRNA 分析中得到了验证。该平台的许多潜在应用包括对 ncRNA 中数十种修饰核糖核苷进行系统水平分析、对新型长 ncRNA 种类进行表征、提高稀有转录变体的检测效率以及对病毒基因组进行分析。