Developing tools for single-molecule sequencing and imaging of RNA modifications
Location: 135 Shillman Hall
Abstract: Despite every cell in the human body having the same genetic makeup, gene expression varies greatly between them. The process of DNA transcription into RNA, along with subsequent post-transcriptional modifications, is crucial for achieving this variability and enabling cell specialization. To manage and potentially correct abnormal gene expression, it’s essential to understand these complex regulatory steps. This understanding relies on developing advanced tools for single-molecule identification, quantification and imaging of RNAs.
In this talk, I will detail our efforts to identify newly modified mRNAs in human cells using direct, long-read sequencing technologies. We are leveraging this technology to explore how RNA modifications impact the physiological functions of developing neurons and immune cells from the human body. By visualizing RNA populations within cells, we can gain insights into their functions and mechanisms—localization often suggests function, while single-cell distribution can reveal underlying mechanisms.
I will also discuss our work on developing methods for site specific imaging of modified and newly transcribed RNAs, including new chemistry designed for live-cell imaging with single-molecule resolution. These innovations promise to deepen our understanding of gene regulation and pave the way for new therapeutic approaches, such as vaccines for infectious disease and advanced gene therapies.
