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Unravelling how over expression of the HAP4 gene operates to extend life span in yeast
Reference
BB/A50027X/1
Principal Investigator / Supervisor
Professor Peter William Piper
Co-Investigators /
Co-Supervisors
Institution
University of Sheffield
Department
Molecular Biology and Biotechnology
Funding type
Research
Value (£)
153,954
Status
Completed
Type
Research Grant
Start date
01/02/2004
End date
31/07/2006
Duration
30 months
Abstract
Our recent data indicates a correlation between the replicative life spans of respirofermentative yeast cells and the levels of respiration in these cells. This study will establish whether this reflects the influences of respiration over redox balance and the Sir2 NAD plus- dependent histone deacetylase. Activity of the latter enzyme is known to slow yeast ageing by suppressing recombination within the repeated ribosomal DNA (rDNA). The degree to which increased mitochondrial respiratory chain activity can slow rDNA recombination, as well as the pro- apoptotic events in old mother cells, will be determined to distinguish whether senescence arises predominantly by genetic instability or proapoptotic events.
Summary
unavailable
Committee
Closed Committee - Genes & Developmental Biology (GDB)
Research Topics
X – not assigned to a current Research Topic
Research Priority
X – Research Priority information not available
Research Initiative
X - not in an Initiative
Funding Scheme
X – not Funded via a specific Funding Scheme
Associated awards:
G17849 Unravelling how overexpression of the HAP4 gene operates to extend life span in yeast
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