Life span extension by targeting a link between metabolism and histone acetylation in Drosophila. (18th January 2016)

• Record Type: Journal Article
• Authors: Peleg, Shahaf; Feller, Christian; Forne, Ignasi; Schiller, Evelyn; Sévin, Daniel C; Schauer, Tamas; Regnard, Catherine; Straub, Tobias; Prestel, Matthias; Klima, Caroline; Schmitt Nogueira, Melanie; Becker, Lore; Klopstock, Thomas; Sauer, Uwe; Becker, Peter B; Imhof, Axel; Ladurner, Andreas G
• Is Part Of: EMBO reports. Volume 17:Number 3(2016:Mar.)
• Page Start: 455
• Page End: 469
• Publication Date: 2016-01-18
• Subjects: ageing -- acetylation -- chromatin -- metabolism; Molecular biology -- Periodicals; Molecular Biology -- Periodicals; Molecular biology; Periodicals; 572.8
• DOI: 10.15252/embr.201541132
• Languages: English
• ISSNs: 1469-221X

Abstract

Abstract: Old age is associated with a progressive decline of mitochondrial function and changes in nuclear chromatin. However, little is known about how metabolic activity and epigenetic modifications change as organisms reach their midlife. Here, we assessed how cellular metabolism and protein acetylation change during early aging in Drosophila melanogaster . Contrary to common assumptions, we find that flies increase oxygen consumption and become less sensitive to histone deacetylase inhibitors as they reach midlife. Further, midlife flies show changes in the metabolome, elevated acetyl‐CoA levels, alterations in protein—notably histone—acetylation, as well as associated transcriptome changes. Based on these observations, we decreased the activity of the acetyl‐CoA‐synthesizing enzyme ATP citrate lyase ( ATPCL ) or the levels of the histone H4 K12‐specific acetyltransferase Chameau. We find that these targeted interventions both alleviate the observed aging‐associated changes and promote longevity. Our findings reveal a pathway that couples changes of intermediate metabolism during aging with the chromatin‐mediated regulation of transcription and changes in the activity of associated enzymes that modulate organismal life span. Synopsis: This study shows that metabolism, acetyl‐CoA levels and histone acetylation are increased during midlife in Drosophila, which correlates with changes in the transcriptome. Depleting the enzymes that link metabolism and histone acetylation reduces midlife acetyl‐CoA levels, transcriptome changes and increases life span. Acetyl‐CoA levels, ATPCL and citrate synthase activity, and protein acetylation are increased in heads of midlife Drosophila males. Lysine deactylase inhibitors rapidly and transiently increase the oxygen consumption rate in Drosophila heads. Quantitation of histone acetylation reveals a transformed histone acetylation signature in midlife male flies. Reducing ATP citrate lyase activity or the levels of the acetyltransferase Chameau extends lifespan in Drosophila males. Abstract : This study shows that metabolism, acetyl‐CoA levels and histone acetylation are increased during midlife in Drosophila, which correlates with changes in the transcriptome. Depleting the enzymes that link metabolism and histone acetylation reduces midlife acetyl‐CoA levels, transcriptome changes and increases lifespan.