The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases.
Sirtuins are a family of phylogenetically conserved nicotinamide adenine dinucleotide-dependent deacetylases that have a firmly established role in aging. Using a simple Saccharomyces cerevisiae yeast heterochromatic derepression assay, we tested a number of environmental chemicals to address the po...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2005-12-01
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| Series: | PLoS Genetics |
| Online Access: | http://europepmc.org/articles/PMC1315280?pdf=render |
| _version_ | 1811232643234136064 |
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| author | Andrew J Olaharski Jasper Rine Brett L Marshall Joshua Babiarz Luoping Zhang Eric Verdin Martyn T Smith |
| author_facet | Andrew J Olaharski Jasper Rine Brett L Marshall Joshua Babiarz Luoping Zhang Eric Verdin Martyn T Smith |
| author_sort | Andrew J Olaharski |
| collection | DOAJ |
| description | Sirtuins are a family of phylogenetically conserved nicotinamide adenine dinucleotide-dependent deacetylases that have a firmly established role in aging. Using a simple Saccharomyces cerevisiae yeast heterochromatic derepression assay, we tested a number of environmental chemicals to address the possibility that humans are exposed to sirtuin inhibitors. Here we show that dihydrocoumarin (DHC), a compound found in Melilotus officinalis (sweet clover) that is commonly added to food and cosmetics, disrupted heterochromatic silencing and inhibited yeast Sir2p as well as human SIRT1 deacetylase activity. DHC exposure in the human TK6 lymphoblastoid cell line also caused concentration-dependent increases in p53 acetylation and cytotoxicity. Flow cytometric analysis to detect annexin V binding to phosphatidylserine demonstrated that DHC increased apoptosis more than 3-fold over controls. Thus, DHC inhibits both yeast Sir2p and human SIRT1 deacetylases and increases p53 acetylation and apoptosis, a phenotype associated with senescence and aging. These findings demonstrate that humans are potentially exposed to epigenetic toxicants that inhibit sirtuin deacetylases. |
| first_indexed | 2024-04-12T11:06:21Z |
| format | Article |
| id | doaj.art-11dfc1c40e8246ecb4ad9f45b795960f |
| institution | Directory Open Access Journal |
| issn | 1553-7390 1553-7404 |
| language | English |
| last_indexed | 2024-04-12T11:06:21Z |
| publishDate | 2005-12-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS Genetics |
| spelling | doaj.art-11dfc1c40e8246ecb4ad9f45b795960f2022-12-22T03:35:44ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042005-12-0116e7710.1371/journal.pgen.0010077The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases.Andrew J OlaharskiJasper RineBrett L MarshallJoshua BabiarzLuoping ZhangEric VerdinMartyn T SmithSirtuins are a family of phylogenetically conserved nicotinamide adenine dinucleotide-dependent deacetylases that have a firmly established role in aging. Using a simple Saccharomyces cerevisiae yeast heterochromatic derepression assay, we tested a number of environmental chemicals to address the possibility that humans are exposed to sirtuin inhibitors. Here we show that dihydrocoumarin (DHC), a compound found in Melilotus officinalis (sweet clover) that is commonly added to food and cosmetics, disrupted heterochromatic silencing and inhibited yeast Sir2p as well as human SIRT1 deacetylase activity. DHC exposure in the human TK6 lymphoblastoid cell line also caused concentration-dependent increases in p53 acetylation and cytotoxicity. Flow cytometric analysis to detect annexin V binding to phosphatidylserine demonstrated that DHC increased apoptosis more than 3-fold over controls. Thus, DHC inhibits both yeast Sir2p and human SIRT1 deacetylases and increases p53 acetylation and apoptosis, a phenotype associated with senescence and aging. These findings demonstrate that humans are potentially exposed to epigenetic toxicants that inhibit sirtuin deacetylases.http://europepmc.org/articles/PMC1315280?pdf=render |
| spellingShingle | Andrew J Olaharski Jasper Rine Brett L Marshall Joshua Babiarz Luoping Zhang Eric Verdin Martyn T Smith The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases. PLoS Genetics |
| title | The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases. |
| title_full | The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases. |
| title_fullStr | The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases. |
| title_full_unstemmed | The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases. |
| title_short | The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases. |
| title_sort | flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases |
| url | http://europepmc.org/articles/PMC1315280?pdf=render |
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