Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.436340
Title: Regulation of Dictyostelium gene expression and chemotaxis by inositol signalling
Author: Keim-Reder, Melanie
ISNI:       0000 0001 3596 4174
Awarding Body: UCL (University College London)
Current Institution: University College London (University of London)
Date of Award: 2006
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Abstract:
The mood-stabilising drugs lithium and valproic acid (VPA) are used in the treatment of bipolar disorder, but the molecular mechanisms underlying their therapeutic effects are not well understood at present. Both drugs have been suggested to attenuate inositol-based signalling: Lithium by depleting the intracellular pool of inositol via uncompetitive inhibition of Inositol monophosphatase (IMPase) and Inositol polyphosphate-1-phosphatase (IPPase), and VPA by inhibition of inositol de novo synthesis. The therapeutic time courses for lithium and VPA treatment suggest that the drugs exert their effects through changing gene expression. Therefore, the aim of the present study was to test the hypothesis that lithium sensitivity in the model system Dictyostelium discoideum (D.discoideum) is caused by changes in gene expression. Real-time PCR and motility assays were used to investigate whether (1) changes in gene expression can be observed in lithium-resistant mutants, (2) overexpression of IMPase and lno1 leads to lithium resistance, and (3) lithium and analogues of the bipolar drug VPA affect gene expression. I found that (1) loss of prolyl oligopeptidase (DpoA) in the lithium resistant LisA mutant or loss of a chromatin-remodelling factor (mutation remains to be confirmed) in the lithium resistant LisG mutant increased lno1 and IPP1 expression. (2) Overexpression of lno1 or IMPase led to resistance against lithium, and also VPA and the VPA-analogue VGD. (3) Lithium and VPA- analogues caused distinct changes in gene expression: Lithium treatment increased the expression of enzymes involved in inositol phosphate signalling, with the exception of IMPase VGD decreased the expression of IMPase, IPP1 and dpoA. In addition, the LisG mutant, which showed increased IPP1 expression, was found to be cross-resistant to VGD. The present study shows that lithium sensitivity in D.discoideum correlates with changes in gene expression and suggests that increase in lno1 and IPP1 expression may confer lithium resistance in D.discoideum.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.436340  DOI: Not available
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