Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.439388
Title: Post-transcriptional control of cyclooxygenase-2
Author: Acton, Stephen Justin
ISNI:       0000 0001 3393 1969
Awarding Body: University of Leicester
Current Institution: University of Leicester
Date of Award: 2007
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Abstract:
Cyclooxygenase-2 is an early response gene that is rapidly and transiently induced by a variety of extracellular ligands in many cell types, including macrophages and mesangial cells. The 3' untranslated region (UTR) of cox-2 mRNA plays a vital role in its post-transcriptional control by regulating mRNA stability and translation. The proximal 60-nucleotides of the 3' UTR contain highly conserved Adenosine-uridine Rich Elements (AREs)---AUUUA, which are known to regulate mRNA stability and translation.;Insertion of the 1--60 sequence was sufficient to cause a marked decrease (>65%) in expression of a luciferase reporter-gene, in both rat mesangial and RAW 264.7 cells. Although reporter-gene constructs proved unresponsive to stimulation with IL1beta in the rat mesangial cells, a response was seen with LPS in the RAW 264.7 cells, which was dependent on the proximal 20 nucleotides of the 1--60 sequence.;Electromobility shift assays revealed that multiple RNA binding proteins, including HuR, TIA-1, TIAR, hnRNP U and AUF1, interacted with this region of the cyclooxygenaase-2 3' TR, with some noticeable differences occurring following removal of the LPS responsive sequence.;These studies provide further evidence of the role played by the 3 ' UTR in the post-transcriptional control of cyclooxygenase-2, as well as identifying several RNA binding proteins likely to be involved in this process.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (M.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.439388  DOI: Not available
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