Yeast replicative aging: a paradigm for defining conserved longevity interventions.
Identifieur interne : 000D77 ( Main/Exploration ); précédent : 000D76; suivant : 000D78Yeast replicative aging: a paradigm for defining conserved longevity interventions.
Auteurs : Brian M. Wasko [États-Unis] ; Matt KaeberleinSource :
- FEMS yeast research [ 1567-1364 ] ; 2014.
Descripteurs français
- KwdFr :
- MESH :
- physiologie : Caenorhabditis elegans, Drosophila, Rodentia, Saccharomyces cerevisiae.
- Animaux, Modèles biologiques.
English descriptors
- KwdEn :
- MESH :
- physiology : Caenorhabditis elegans, Drosophila, Rodentia, Saccharomyces cerevisiae.
- Animals, Models, Biological.
Abstract
The finite replicative life span of budding yeast mother cells was demonstrated as early as 1959, but the idea that budding yeast could be used to model aging of multicellular eukaryotes did not enter the scientific mainstream until relatively recently. Despite continued skepticism by some, there are now abundant data that several interventions capable of extending yeast replicative life span have a similar effect in multicellular eukaryotes including nematode worms, fruit flies, and rodents. In particular, dietary restriction, mTOR signaling, and sirtuins are among the most studied longevity interventions in the field. Here, we describe key conserved longevity pathways in yeast and discuss relationships that may help explain how such broad conservation of aging processes could have evolved.
DOI: 10.1111/1567-1364.12104
PubMed: 24119093
PubMed Central: PMC4134429
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Wasko</name><affiliation wicri:level="4"><nlm:affiliation>Department of Pathology, University of Washington, Seattle, WA, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Pathology, University of Washington, Seattle, WA</wicri:regionArea><placeName><region type="state">Washington (État)</region><settlement type="city">Seattle</settlement></placeName><orgName type="university">Université de Washington</orgName></affiliation></author><author><name sortKey="Kaeberlein, Matt" sort="Kaeberlein, Matt" uniqKey="Kaeberlein M" first="Matt" last="Kaeberlein">Matt Kaeberlein</name></author></analytic><series><title level="j">FEMS yeast research</title><idno type="eISSN">1567-1364</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals (MeSH)</term><term>Caenorhabditis elegans (physiology)</term><term>Drosophila (physiology)</term><term>Models, Biological (MeSH)</term><term>Rodentia (physiology)</term><term>Saccharomyces cerevisiae (physiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux (MeSH)</term><term>Caenorhabditis elegans (physiologie)</term><term>Drosophila (physiologie)</term><term>Modèles biologiques (MeSH)</term><term>Rodentia (physiologie)</term><term>Saccharomyces cerevisiae (physiologie)</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Caenorhabditis elegans</term><term>Drosophila</term><term>Rodentia</term><term>Saccharomyces cerevisiae</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Caenorhabditis elegans</term><term>Drosophila</term><term>Rodentia</term><term>Saccharomyces cerevisiae</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Models, Biological</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Modèles biologiques</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The finite replicative life span of budding yeast mother cells was demonstrated as early as 1959, but the idea that budding yeast could be used to model aging of multicellular eukaryotes did not enter the scientific mainstream until relatively recently. Despite continued skepticism by some, there are now abundant data that several interventions capable of extending yeast replicative life span have a similar effect in multicellular eukaryotes including nematode worms, fruit flies, and rodents. In particular, dietary restriction, mTOR signaling, and sirtuins are among the most studied longevity interventions in the field. Here, we describe key conserved longevity pathways in yeast and discuss relationships that may help explain how such broad conservation of aging processes could have evolved. </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">24119093</PMID><DateCompleted><Year>2015</Year><Month>08</Month><Day>07</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1567-1364</ISSN><JournalIssue CitedMedium="Internet"><Volume>14</Volume><Issue>1</Issue><PubDate><Year>2014</Year><Month>Feb</Month></PubDate></JournalIssue><Title>FEMS yeast research</Title><ISOAbbreviation>FEMS Yeast Res</ISOAbbreviation></Journal><ArticleTitle>Yeast replicative aging: a paradigm for defining conserved longevity interventions.</ArticleTitle><Pagination><MedlinePgn>148-59</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/1567-1364.12104</ELocationID><Abstract><AbstractText>The finite replicative life span of budding yeast mother cells was demonstrated as early as 1959, but the idea that budding yeast could be used to model aging of multicellular eukaryotes did not enter the scientific mainstream until relatively recently. Despite continued skepticism by some, there are now abundant data that several interventions capable of extending yeast replicative life span have a similar effect in multicellular eukaryotes including nematode worms, fruit flies, and rodents. In particular, dietary restriction, mTOR signaling, and sirtuins are among the most studied longevity interventions in the field. Here, we describe key conserved longevity pathways in yeast and discuss relationships that may help explain how such broad conservation of aging processes could have evolved. </AbstractText><CopyrightInformation>© 2013 Federation of European Microbiological Societies. Published by John Wiley & Sons Ltd. 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IdType="pubmed">8186460</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country><region><li>Washington (État)</li></region><settlement><li>Seattle</li></settlement><orgName><li>Université de Washington</li></orgName></list><tree><noCountry><name sortKey="Kaeberlein, Matt" sort="Kaeberlein, Matt" uniqKey="Kaeberlein M" first="Matt" last="Kaeberlein">Matt Kaeberlein</name></noCountry><country name="États-Unis"><region name="Washington (État)"><name sortKey="Wasko, Brian M" sort="Wasko, Brian M" uniqKey="Wasko B" first="Brian M" last="Wasko">Brian M. 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