About this Research Topic
There are over 170 types of RNA modifications on coding and noncoding RNAs. Nonetheless, most of them are still poorly studied. Thus, profiling epitranscriptomics of various modifications by novel methods and characterization of their regulators are of great importance. On the other hand, more comprehensive investigations on the regulation and functions of RNA modifications, including that of m6A, in normal development and disease settings, and translation of such knowledge into clinical practice, are still needed.
In this Research Topic, we aim to publish innovative research from basic science to translational research on RNA modifications. Original Research, Methods, Review, Mini-Review and perspective are all welcome. The subjects we wish to cover will include but are not limited to the following:
• Characterization of regulators of RNA modifications and their functions in gene expression control;
• Methods to detect or modulate RNA modifications, such as profiling of epitranscriptome by web-lab and dry-lab methods, imaging of RNA modifications, and programmable editing of RNA modifications;
• The functions and mechanisms of RNA modifications in physiological processes, such as hematopoiesis, development, reproduction, and immune response;
• The functions and mechanisms of RNA modifications in human diseases, such as cancers, diabetes, cardiovascular disease, degenerative disease, and viral disease;
• The application of RNA modifications and/or their regulators as clinical biomarkers;
• Development of specific inhibitors or other innovative approaches to target RNA modifications for a therapeutic purpose;
• Combined therapy based on RNA modification targeting.
Keywords: RNA modifications, Epitranscriptomics, Noncoding RNA, Stem cell, Development, Cancer, Virus infection, Biomarker, Targeted therapy
Important Note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.