Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.622057
Title: Identification and characterization of novel histone modifications during cellular senescence
Author: Manoharan, Indrani
ISNI:       0000 0004 5360 8394
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 2014
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Abstract:
Cellular senescence is a stable cell cycle arrest and can be triggered by various signals including telomere shortening, oncogenic activation and other stress activators. Senescence is accompanied by changes in the cellular organization, gene expression and induction of the secretome. It is established and maintained by at least two major tumor suppressor pathways, the p53-p21 and p16-pRB pathways. Senescence is now recognized as a potent barrier to tumor progression and is directly and indirectly linked to a large array of age-related pathologies. However the precise molecular mechanisms of senescence, particularly how cells are driven into irreversible proliferation arrest, in not fully understood. It is well known that widespread changes in the chromatin structure of senescence contribute to the senescent phenotype. In line with this, the primary objective of this project is to understand how senescence is regulated by its chromatin structure. I have focussed on the identification and characterization of novel histone modifications that occur during senescence. Large-scale profiling of histone modifications was performed in replicatively senescent cells in comparison to proliferating cells. Candidate histone modifications were identified that alter during senescence from the screen. To our knowledge, this is the first study to have implied a novel role for these histone modifications during senescence. Also a third histone modification, H4K16ac, was chosen for study based on ChIP-seq observations made in the lab. The mark has also been extensively linked to cancer and aging. All together, work from this project imparts new knowledge on how certain novel histone modifications might regulate senescence via critical modulation of its chromatin structure and how they may impinge on senescence-associated effects such as ageing and cancer.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.622057  DOI: Not available
Keywords: QH345 Biochemistry
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