Dr David ClancyLecturer
My aim is to delay the onset of ageing-related changes so that healthy lifespan is extended. Therefore I investigate the basic biology of ageing, which includes a search for reliable predictive biomarkers of ageing, from the behavioural to the molecular. To test potential drug targets I use the model organism Drosophila, altering expression of potentially ageing-relevant genes during adulthood, thus mimicking drug treatment.
Mimicking drug treatment by restoring youthful expression levels of ageing-relevant genes
Some genes change expression directionally with age, thus they are related to the ageing process either causally or consequentially. Most will be consequentially. If we extend lifespan using dietary restriction (DR) and measure gene expression and we see similar patterns of directional change in DR and control-fed flies, then these genes might be more likely to be causally associated with the ageing process. In the graphs below, gene expression between feeding regimes is different when measured using chronological time but when measured against cohort mortality, a proxy for physiological age (i.e. proportion of ultimate lifespan the animal/cohort has lived) the expression patterns are the same.
From Scott Pletcher’s paper in Current Biology (2002), data from http://www.hcoa.org/scott/
I plan to use transgenic flies to maintain expression of specific ageing-relevant genes at young adult levels. By doing this I hope to achieve extension of healthy lifespan. The approach mimics a drug therapy approach to reduce or ameliorate the negative effects of age. The genes I will test all have human homologs which are either associated directly with ageing or with ageing-related morbidity, such as heart attack and Alzheimers Dementia. This work is funded by the charity Help the Aged/Age Concern.
Ageing (Aging – I side with the Americans here)
Evolutionary theory tells us why we age. So, while we know, therefore, that the answers are ultimately genetic, we don’t know what makes us age, how our genes allow the ageing process to progress, and how genetic differences can cause huge differences in lifespans between species. Understanding the causes of ageing is one of the last great mysteries in biology. The best way to measure ageing is to measure lifespan. And to study the genetics of ageing there is probably no better model organism than the fly Drosophila melanogaster.
Insulin-like signalling and ageing
These female flies opposite have a mean lifespan difference of nearly 40% as a result of a single gene knocked out in the insulin/insulin-like signalling pathway. The one on the left lives longer; the gene knockout results in dwarfism as well as longevity. This work was done from 1998-2001 in Linda Partridge’s lab at University College London, and showed the importance of this pathway in modulating survival, an effect which is evolutionarily conserved from worms and flies through to mammals, and almost certainly humans. Funded by BBSRC.
The effects of mitochondrial genotype on ageing and lifespanControlling the nuclear genetic background to a much greater degree than previously achieved, I compared the effects on lifespan of a range of different mitochondrial genotypes. In real world terms this work suggested that, while it is possible for mitochondrial type (even single altered amino acids) to have very large lifespan effects, this may be uncommon.
This figure shows the effects on cohort survival of three different mitochondria on a single nuclear background (from a Hawaii strain). Between the Alstonville and Japan mitochondrial genomes that code for proteins there is only one amino acid difference (ND2: His182?Tyr). However these mitochondria on seven other nuclear genetic backgrounds showed very minor lifespan effects. This work was done at Monash University, Melbourne, Australia, from 2003-2006, funded by the Australian Research Council.
Because mitochondria are transmitted by females, not males, they avoid any natural selection in males. Using the strains I made during this work, the effect of this on males was elegantly demonstrated recently by Damian Dowling in an article in Science. He showed that mitochondrial genomes can have significant negative effects in males (especially reproductive), but not in females.
Planned work – including student projects
- Testing a variety of genes for effects on health and lifespan (U/G or MSc project, or PhD project)
- Testing biomarkers of ageing in Drosophila (U/G or MSc project, or PhD project)
- Examining the role of membrane lipids in ageing (U/G or MSc project, or PhD project)
- Cryogenic preservation of Drosophila embryos (U/G or MSc project, or PhD project)
- How does early life diet affect lifespan in Drosophila? (U/G or MSc project, or PhD project)
- What cuases oxidative stress, and what helps and hinders repair? (U/G or MSc project, or PhD project)
Aspirational work (collaborators needed)
Metabolomics of ageing in the rat
Interested students should email me for further information and reading on these topics, or come and see me. Note that currently, PhD students would need to be self-supporting.
Early work - Wolbachia
In 1991 I began studying the Wolbachia endoparasite in Drosophila under Ary Hoffmann in Melbourne, Australia:Wolbachia (seen in red clustering about the poles of Drosophila embryonic nuclei pre-mitosis) infects a very large number and variety of terrestrial insects, isopod, mites, nematodes and other hosts, drastically altering their reproduction in order to spread itself through populations. In 1997 I confidently predicted that the phenomenon was of academic interest only and its popularity would wane. This graph above shows the extent to which interest waned. In fact Wolbachia is currently being trialed as a method to control the major mosquito vector of the dengue fever virus. Who knew? In fact, interest really took off about the time I stopped studying it. Clearly I was holding the field back.
Still, no-one has done the really interesting thing, which is to work out how Wolbachia alters host reproduction...
PhD Supervision Interests
Age is the major risk factor for the major causes of death in humans. Therefore I investigate the basic biology and the genetics of ageing. This is known as Biogerontology. My aim is to delay the onset of ageing-related changes so that healthy lifespan is extended. To discover and test potential drug targets and therapies I use the model organism Drosophila. I welcome enquiries from students interested in this rapidly moving and very exciting area.
Complete mitochondrial genome sequences of thirteen globally sourced strains of fruit fly (Drosophila melanogaster) form a powerful model for mitochondrial research
Wolff, J.N., Camus, M.F., Clancy, D.J., Dowling, D.K. 12/2016 In: Mitochondrial DNA. 27, 6, p. 4672-4674. 3 p.
Flies, worms and the Free Radical Theory of ageing
Clancy, D., Birdsall, J. 01/2013 In: Ageing Research Reviews. 12, 1, p. 404-412. 9 p.
Reliability and variability of sleep and activity as biomarkers of ageing in Drosophila
Koudounas, S., Green, E.W., Clancy, D. 10/2012 In: Biogerontology. 13, 5, p. 489-499. 11 p.
Mitochondria, maternal inheritance, and male aging
Camus, M.F., Clancy, D.J., Dowling, D.K. 2012 In: Current Biology. 22, 18, p. 1717-1721. 5 p.
Cytoplasmic male sterility in Drosophila melanogaster associated with a mitochondrial CYTB variant
Clancy, D.J., Hime, G.R., Shirras, A.D. 10/2011 In: Heredity. 107, 4, 3 p.
Mitochondrial DNA variants in Drosophila melanogaster are expressed at the level of the organismal phenotype
Aw, W.C., Correa, C.C., Clancy, D.J., Ballard, J.W.O. 09/2011 In: Mitochondrion. 11, 5, p. 756-763. 8 p.
DmWRNexo is a 3'aEuro"5' exonuclease: phenotypic and biochemical characterization of mutants of the Drosophila orthologue of human WRN exonuclease
Boubriak, I., Mason, P.A., Clancy, D.J., Dockray, J., Saunders, R.D.C., Cox, L.S. 06/2009 In: Biogerontology. 10, 3, p. 267-277. 11 p.
Genome instability in Drosophila mutant for WRN-like exonuclease
Boubriak, I., Clancy, D.J., Borer, C., Saunders, R.D.C., Cox, L.S. 01/2009 In: Mutagenesis. 24, 1, 2 p.
Variation in mitochondrial genotype has substantial lifespan effects which may be modulated by nuclear background
Clancy, D.J. 12/2008 In: Aging Cell. 7, 6, p. 795-804. 10 p.
Identification and characterization of a Drosophila ortholog of WRN exonuclease that is required to maintain genome integrity
Saunders, R.D.C., Boubriak, I., Clancy, D.J., Cox, L.S. 06/2008 In: Aging Cell. 7, 3, p. 418-425. 8 p.
Modeling Werner Syndrome in Drosophila melanogaster: hyper-recombination in flies lacking WRN-like exonuclease
Cox, L.S., Clancy, D.J., Boubriak, I., Saunders, R.D. 11/2007 In: Annals of the New York Academy of Sciences. 1119, p. 274-288. 15 p.
Water balance and cation levels in Drosophila: can early physiological decline predict aging and longevity?
Johnson, T.K., McKechnie, S.W., Clancy, D.J. 02/2006 In: Journals of Gerontology, Series A. 61, 2, p. 146-152. 7 p.
Metabolic rate is not reduced by dietary-restriction or by lowered insulin/IGF-1 signalling and is not correlated with individual lifespan in Drosophila melanogaster
Hulbert, A.J., Clancy, D.J., Mair, W., Braeckman, B.P., Gems, D., Partridge, L. 08/2004 In: Experimental Gerontology. 39, 8, p. 1137-1143. 7 p.
Dietary restriction and life-span - Response
Clancy, D.J., Gems, D., Hafen, E., Leevers, S.J., Partridge, L. 21/06/2002 In: Science. 296, 5576, p. 2141-2142. 2 p.
Dietary restriction in long-lived dwarf flies
Clancy, D.J., Gems, D., Hafen, E., Leevers, S.J., Partridge, L. 12/04/2002 In: Science. 296, 5566, p. 319. 1 p.
Identifying common determinants of lifespan and ageing in model organisms
Clancy, D.J., Keaney, M., Leevers, S.J., Partridge, L., Gems, D. 02/2002 In: Mechanisms of Development. 123, 4, p. 441-442. 2 p.
Extension of life-span by loss of CHICO, a Drosophila insulin receptor substrate protein
Clancy, D.J., Gems, D., Harshman, L.G., Oldham, S., Stocker, H., Hafen, E., Leevers, S.J., Partridge, L. 6/04/2001 In: Science. 292, 5514, p. 104-106. 3 p.
A simple method to achieve consistent larval density in bottle cultures.
Clancy, D.J., Kennington, W.J. 2001 In: Drosophila Information Service. 84, p. 168-169. 2 p.
Environmental effects on cytoplasmic incompatibility and bacterial load in Wolbachia-infected Drosophila simulans
Clancy, D.J., Hoffmann, A.A. 01/1998 In: Entomologia Experimentalis et Applicata. 86, 1, p. 13-24. 12 p.
Behavior of Wolbachia endosymbionts from Drosophila simulans in Drosophila serrata, a novel host
Clancy, D.J., Hoffmann, A.A. 05/1997 In: The American Naturalist. 149, 5, p. 975-988. 14 p.
Cytoplasmic incompatibility in Drosophila simulans: evolving complexity
Clancy, D.J., Hoffmann, A.A. 04/1996 In: Trends in Ecology and Evolution. 11, 4, p. 145-146. 2 p.
Naturally-occurring Wolbachia infection in Drosophila simulans that does not cause cytoplasmic incompatibility
Hoffmann, A.A., Clancy, D., Duncan, J. 1996 In: Heredity. 76, p. 1-8. 8 p.
Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster
Hoffmann, A.A., Clancy, D.J., Merton, E. 1994 In: Genetics. 136, 3, p. 993-999. 7 p.