Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.505280
Title: The role of CBP and p300 in Alzheimer's Disease
Author: Francis, Yitshak Itsik
Awarding Body: University of London
Current Institution: University College London (University of London)
Date of Award: 2008
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Abstract:
Studies of the mechanisms underlying memory formation have defined central roles for CRE-dependent gene expression, which is mediated by the transcription factor CREB and the coactivator CBP. CBP creates a bridge between CREB and the basal transcriptional machinery and acetylates histones, which induces chromosomal changes and results in loss of chromosomal repression. This allows successful transcription of the underlying genes needed for synthesis of proteins underlying memory formation. CBP has been linked to neurodegenerative diseases and cerebral CBP levels were shown to reduce in mice lacking functional presenilins (PSs), a class of enzymes that has been associated with Alzheimer's Disease (AD). In this thesis it is shown that WT PS1 stimulates the transcriptional activating ability of CBP and its close homolog p300, whereas an Alzheimer's disease- associated N terminal mutant of PS1 did not produce this effect. Interestingly, PS1 C terminal mutants produced a reduction in CBP transcriptional activating ability, compared to control levels. Additionally, we showed that wild type PS1 increases the endogenous CBP level. Moreover, an increase in CBP endogenous levels was noted when the cells were transfected with the -M146L N-terminal mutant of PSI. However, these levels were still significantly lower when compared to cells transfected with wild type PSI. We were also able to show that knockdown of endogenous PSI leads to a decrease in endogenous CBP levels and a decrease in CBP activity. Hence, PSI can affect both the level and the activity of CBP. In addition, the activation of CBP by WT PSI involves the PI 3-kinase, p38 MAP kinase and p42/p44 MAP kinase pathways and targets primarily the C terminus of CBP. It is also shown that the effect of wild-type PSI is dependent on the histone acetyltransferase activity (HAT) of CBP. Moreover, it was demonstrated that WT PSI, but not its M146L mutant, could increase the promoter activity of c-fos, a CBP HAT dependent target gene. Additionally, we showed that application of the histone deacetylase inhibitor, TSA, rescued the long-term potentiation and long-term memory defects shown by APP/PS1 mutant mice. Moreover, it was shown that the acetylation level of histone H4 in APP/PS1 mice is lower than that of WT littermates and that TSA injection restores the acetylation of these histones. This is the first study to identify AD as a disease of epigenetic etiology and suggests that enhancing histone acetylation may have potential for the treatment of AD.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.505280  DOI: Not available
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