Show simple item record

dc.contributor.advisorAthma Paien_US
dc.contributor.authorTorres Ulloa, Leslie
dc.date.accessioned2024-06-07T18:04:25Z
dc.date.available2024-06-07T18:04:25Z
dc.date.issued2024-05-31
dc.identifier.doi10.13028/3wex-np87
dc.identifier.urihttp://hdl.handle.net/20.500.14038/53427
dc.description.abstract3’ end cleavage and polyadenylation are required steps in pre-mRNA maturation. The rate at which 3’ end cleavage occurs can determine the temporal availability of mRNA for subsequent function throughout the cell and is likely tightly regulated. While there are numerous high-throughput methods for global profiling of RNA maturation rates, the study of pre-mRNA 3’ end cleavage kinetics has remained limited to low-throughput approaches, and the temporal regulation of polyadenylation site choice that determines the composition of the 3’ UTRs of mRNAs remains poorly understood. This research project seeks to address this gap by introducing a novel genome-wide, site-specific methodology for estimating rates of pre-mRNA 3’ end cleavage, using metabolic labeling of nascent RNA, high-throughput sequencing, and mathematical modeling. Using in-silico simulations of nascent RNA-seq data, we show that our approach can accurately and precisely estimate cleavage half-lives for both constitutive and alternative sites. In Drosophila melanogaster S2 cells, we find that cleavage rates are fast but highly variable across sites, with alternative events being slowest. This variability in rates is underpinned by distinctive sequence elements, where an A-rich region upstream of the cleavage site, a U-rich element downstream of the cleavage site, and a higher density of polyadenylation signals, lead to faster cleavage reactions. Assessment of Polymerase II dynamics around cleavage sites reveals that cleavage rates are associated with the localization of RNA Polymerase II at the end of a gene and faster cleavage leads to quicker degradation of downstream read-through RNA. This approach for estimating pre-mRNA 3’ end cleavage kinetics opens new possibilities in the study of co-transcriptional regulation of mRNA expression and transcription termination across cellular states.en_US
dc.language.isoen_USen_US
dc.publisherUMass Chan Medical Schoolen_US
dc.relation<p>The published article associated with this dissertation is: Torres-Ulloa L, Calvo-Roitberg E, Pai AA. <a href="https://doi.org/10.1261/rna.079783.123" target="_blank">Genome-wide kinetic profiling of pre-mRNA 3' end cleavage</a>. RNA. 2024 Feb 16;30(3):256-270. doi: 10.1261/rna.079783.123. PMID: 38164598; PMCID: PMC10870368.</p>en_US
dc.rightsCopyright © 2024 Leslie Torres Ulloaen_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/en_US
dc.subjectRNA processingen_US
dc.subject3' end cleavageen_US
dc.subjectcleavage and polyadenylationen_US
dc.subjectmRNA processingen_US
dc.titleKinetics of Pre-mRNA 3’ End Cleavageen_US
dc.typeDoctoral Dissertationen_US
refterms.dateFOA2024-06-07T18:04:27Z
atmire.contributor.authoremailLeslie.TorresUlloa@umassmed.eduen_US
dc.contributor.departmentRNA Therapeutics Instituteen_US
dc.description.thesisprogramInterdisciplinary Graduate Programen_US
dc.identifier.orcid0000-0002-8026-1926en_US


Files in this item

Thumbnail
Name:
LTorres_Ulloa_DISSERTATION_rev ...
Size:
2.144Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record

Copyright © 2024 Leslie Torres Ulloa
Except where otherwise noted, this item's license is described as Copyright © 2024 Leslie Torres Ulloa