Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774310
Title: Investigating the link between translation and nonsense-mediated mRNA decay
Author: Petrić Howe, Marija
ISNI:       0000 0004 7961 5162
Awarding Body: University of Birmingham
Current Institution: University of Birmingham
Date of Award: 2019
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Thesis embargoed until 27 Sep 2022
Access from Institution:
Abstract:
Nonsense mediated mRNA decay (NMD) is regarded as an active cellular surveillance mechanism that eliminates mRNAs that contain a premature translation termination codon (PTC). In this study, I present an alternative hypothesis, formulated as the ribosome release model, which proposes that NMD may occur as a passive consequence of general roles that NMD factors play in ribosome release upon translation termination. I tested this directly, by looking at whether NMD factors affect NMD reporter mRNA association with the ribosomes. I also analysed the role of NMD factors in general translation and their association with translating mRNAs. My data indicates that NMD factors do bind mRNAs undergoing translation, regulating translation of many transcripts, and indeed possibly triggering ribosome release from mRNAs upon termination. Additionally, I found that UPF1 associates with ribosome-free RNA granules in the cell, into which in stress conditions, when global translation is impaired, it almost entirely re-distributes, possibly sequestering translationally repressed mRNAs from the translational pool. Finally, whilst investigating the role of NMD factors in translation by means of a puromycylation assay, I made unexpected observations that indicate that many complete proteins can be released from the ribosome with a tRNA still attached to the last C-terminal amino acid.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.774310  DOI: Not available
Keywords: QR Microbiology
Share: