2026-09-19T20:12:48Zhttps://dspace.mit.edu/server/oai/requestoai:dspace.mit.edu:1721.1/1527222023-11-03T03:08:33Zcom_1721.1_7582com_1721.1_7581col_1721.1_131022
Bathe, Mark
Rouskin, Silvi
Allan, Matthew F.
Massachusetts Institute of Technology. Computational and Systems Biology Program
2023-11-02T20:11:04Z
2023-11-02T20:11:04Z
2023-09
2023-10-27T22:06:54.119Z
https://hdl.handle.net/1721.1/152722
0000-0001-8182-7402
Ribonucleic acid (RNA) performs versatile, essential functions in all known organisms and viruses. These functions require the RNA to fold into specific secondary and tertiary structures, and in many cases to switch among multiple structural states. Predicting and experimentally determining RNA structures remains challenging, particularly because of this propensity of one RNA sequence to form a heterogeneous ensemble of structures.
This thesis investigates two related problems in RNA folding. First, a method of nucleic acid origami is developed in which four divergent RNA sequences are reprogrammed by short antisense oligonucleotides (ASOs) to fold into six different 3D wireframe polyhedra. How each type of structural feature in the polyhedra affects the stability of local base pairs is revealed using dimethyl sulfate mutational profiling with sequencing (DMS-MaPseq). Second, the structural ensembles formed by the genome of SARS coronavirus 2 (SARSCoV-2) are investigated using DMS-MaPseq. In particular, a method for detecting long-range RNA:RNA interactions using ASOs is developed and applied to pinpoint an interaction between the frameshifting stimulation element (FSE) and a sequence of RNA over one kilobase downstream, which occurs in nearly half of the RNA molecules. This technique is expanded to reveal long-range interactions in three additional coronaviruses, suggesting that this type of RNA structure is more common than previously thought.
Overall, this thesis uses ASOs and mutational profiling to reprogram and investigate RNA folding. A wide variety of RNA sequences prove amenable to these techniques, which enable the creation of synthetic RNA structures and the characterization of natural ones including long-range RNA:RNA interactions. The results of this study enable future investigations on developing RNA origami for research and therapeutic applications and on the roles of distant RNA elements in regulating ribosomal frameshifting in coronaviruses.
Ph.D.
Massachusetts Institute of Technology
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https://rightsstatements.org/page/InC-EDU/1.0/
Investigating and Reprogramming RNA Folding with Molecular Probes
Thesis
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Doctoral
Doctor of Philosophy
Publication
unknown
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<Abstract>Ribonucleic acid (RNA) performs versatile, essential functions in all known organisms and viruses. These functions require the RNA to fold into specific secondary and tertiary structures, and in many cases to switch among multiple structural states. Predicting and experimentally determining RNA structures remains challenging, particularly because of this propensity of one RNA sequence to form a heterogeneous ensemble of structures.
This thesis investigates two related problems in RNA folding. First, a method of nucleic acid origami is developed in which four divergent RNA sequences are reprogrammed by short antisense oligonucleotides (ASOs) to fold into six different 3D wireframe polyhedra. How each type of structural feature in the polyhedra affects the stability of local base pairs is revealed using dimethyl sulfate mutational profiling with sequencing (DMS-MaPseq). Second, the structural ensembles formed by the genome of SARS coronavirus 2 (SARSCoV-2) are investigated using DMS-MaPseq. In particular, a method for detecting long-range RNA:RNA interactions using ASOs is developed and applied to pinpoint an interaction between the frameshifting stimulation element (FSE) and a sequence of RNA over one kilobase downstream, which occurs in nearly half of the RNA molecules. This technique is expanded to reveal long-range interactions in three additional coronaviruses, suggesting that this type of RNA structure is more common than previously thought.
Overall, this thesis uses ASOs and mutational profiling to reprogram and investigate RNA folding. A wide variety of RNA sequences prove amenable to these techniques, which enable the creation of synthetic RNA structures and the characterization of natural ones including long-range RNA:RNA interactions. The results of this study enable future investigations on developing RNA origami for research and therapeutic applications and on the roles of distant RNA elements in regulating ribosomal frameshifting in coronaviruses.</Abstract>
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