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Old 23rd April 2012, 10:24 AM
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Default Researchers have identified key genes that switch off with aging

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ScienceDaily (Apr. 19, 2012) — Researchers have identified key genes that switch off with aging, highlighting them as potential targets for anti-aging therapies.
Researchers at King's College London, in collaboration with the Wellcome Trust Sanger Institute, have identified a group of 'aging' genes that are switched on and off by natural mechanisms called epigenetic factors, influencing the rate of healthy aging and potential longevity.
The study also suggests these epigenetic processes -- that can be caused by external factors such as diet, lifestyle and environment -- are likely to be initiated from an early age and continue through a person's life. The researchers say that the epigenetic changes they have identified could be used as potential 'markers' of biological aging and in the future could be possible targets for anti-aging therapies.
Published April 20 in PLoS Genetics, the study looked at 172 twins aged 32 to 80 from the TwinsUK cohort based at King's College London and St Thomas' Hospital, as part of King's Health Partners Academic Health Sciences Centre.
The researchers looked for epigenetic changes in the twins' DNA, and performed epigenome-wide association scans to analyze these changes in relation to chronological age. They identified 490 age related epigenetic changes. They also analysed DNA modifications in age related traits and found that epigenetic changes in four genes relate to cholesterol, lung function and maternal longevity.
To try to identify when these epigenetic changes may be triggered, the researchers replicated the study in 44 younger twins, aged 22 to 61, and found that many of the 490 age related epigenetic changes were also present in this younger group. The researchers say these results suggest that while many age related epigenetic changes happen naturally with age throughout a person's life, a proportion of these changes may be initiated early in life.
Dr Jordana Bell from King's College London, who co-led the study said: 'We found that epigenetic changes associate with age related traits that have previously been used to define biological age.
'We identified many age-related epigenetic changes, but four seemed to impact the rate of healthy aging and potential longevity and we can use these findings as potential markers of aging. These results can help understand the biological mechanisms underlying healthy aging and age-related disease, and future work will explore how environmental effects can affect these epigenetic changes.'
Dr Panos Deloukas, co-leader of the study from the Wellcome Trust Sanger Institute, said: 'Our study interrogated only a fraction of sites in the genome that carry such epigenetic changes; these initial findings support the need for a more comprehensive scan of epigenetic variation.'
Professor Tim Spector, senior author from King's College London, said: 'This study is the first glimpse of the potential that large twin studies have to find the key genes involved in aging, how they can be modified by lifestyle and start to develop anti-aging therapies. The future will be very exciting for age research.'
http://www.sciencedaily.com/releases...0419191709.htm

Bell, J. T., P.-C. Tsai, et al. (2012). "Epigenome-Wide Scans Identify Differentially Methylated Regions for Age and Age-Related Phenotypes in a Healthy Ageing Population." PLoS Genet 8(4): e1002629.
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Age-related changes in DNA methylation have been implicated in cellular senescence and longevity, yet the causes and functional consequences of these variants remain unclear. To elucidate the role of age-related epigenetic changes in healthy ageing and potential longevity, we tested for association between whole-blood DNA methylation patterns in 172 female twins aged 32 to 80 with age and age-related phenotypes. Twin-based DNA methylation levels at 26,690 CpG-sites showed evidence for mean genome-wide heritability of 18%, which was supported by the identification of 1,537 CpG-sites with methylation QTLs in cis at FDR 5%. We performed genome-wide analyses to discover differentially methylated regions (DMRs) for sixteen age-related phenotypes (ap-DMRs) and chronological age (a-DMRs). Epigenome-wide association scans (EWAS) identified age-related phenotype DMRs (ap-DMRs) associated with LDL (STAT5A), lung function (WT1), and maternal longevity (ARL4A, TBX20). In contrast, EWAS for chronological age identified hundreds of predominantly hyper-methylated age DMRs (490 a-DMRs at FDR 5%), of which only one (TBX20) was also associated with an age-related phenotype. Therefore, the majority of age-related changes in DNA methylation are not associated with phenotypic measures of healthy ageing in later life. We replicated a large proportion of a-DMRs in a sample of 44 younger adult MZ twins aged 20 to 61, suggesting that a-DMRs may initiate at an earlier age. We next explored potential genetic and environmental mechanisms underlying a-DMRs and ap-DMRs. Genome-wide overlap across cis-meQTLs, genotype-phenotype associations, and EWAS ap-DMRs identified CpG-sites that had cis-meQTLs with evidence for genotype–phenotype association, where the CpG-site was also an ap-DMR for the same phenotype. Monozygotic twin methylation difference analyses identified one potential environmentally-mediated ap-DMR associated with total cholesterol and LDL (CSMD1). Our results suggest that in a small set of genes DNA methylation may be a candidate mechanism of mediating not only environmental, but also genetic effects on age-related phenotypes.
http://www.plosgenetics.org/article/...l.pgen.1002629
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