Repository logo

Single-Molecule RNA Sizing Enables Quantitative Analysis of Alternative Transcription Termination

Accepted version

Change log


Patino Guillen, Gerardo 
Pešović, Jovan 
Panić, Marko 
Savić-Pavićević, Dušanka 
Bošković, Filip 


Transcription, a critical process in molecular biology, has found many applications in RNA synthesis, including mRNA vaccines and RNA therapeutics. However, current RNA characterization technologies suffer from amplification and enzymatic biases that lead to loss of native information. Here, we introduce a strategy to quantitatively study both transcription and RNA polymerase behaviour by sizing RNA with RNA nanotechnology and nanopores. To begin, we utilized T7 RNA polymerase to transcribe linear DNA lacking termination sequences. Surprisingly, we discovered alternative transcription termination in the origin of replication sequence. Next, we employed circular DNA without transcription terminators to perform rolling circle transcription. This allowed us to gain valuable insights into the processivity and transcription behaviour of RNA polymerase at the single-molecule level. Our work demonstrates how RNA nanotechnology and nanopores may be used in tandem for the direct and quantitative analysis of RNA transcripts. This methodology provides a promising pathway for accurate RNA structural mapping by enabling the study of full-length RNA transcripts at the single-molecule level.



Journal Title

Nature Communications

Conference Name

Journal ISSN


Volume Title


Nature Portfolio

Publisher DOI

Publisher URL

European Research Council (ERC) consolidator grant (DesignerPores no. 647144), ERC-2019-PoC grant (PoreDetect no. 899538), EPSRC CDT MRes/PhD Studentship in Nanoscience and Nanotechnology (NanoDTC Cambridge EP/S022953/1), Trinity-Henry Barlow Scholarship, George and Lilian Schiff Foundation Studentship, Winton Programme for the Physics of Sustainability PhD Scholarship, St John’s College Benefactors’ Scholarship, Science Fund of the Republic of Serbia, Grant No. 7754217, READ-DM1.