Quasi-programmed aging of budding yeast: a trade-off between programmed processes of cell proliferation, differentiation, stress response, survival and death defines yeast lifespan.
Identifieur interne : 000E30 ( Main/Exploration ); précédent : 000E29; suivant : 000E31Quasi-programmed aging of budding yeast: a trade-off between programmed processes of cell proliferation, differentiation, stress response, survival and death defines yeast lifespan.
Auteurs : Anthony Arlia-Ciommo ; Amanda Piano ; Anna Leonov ; Veronika Svistkova ; Vladimir I. TitorenkoSource :
- Cell cycle (Georgetown, Tex.) [ 1551-4005 ] ; 2014.
Descripteurs français
- KwdFr :
- Mitochondries (génétique), Mitochondries (métabolisme), Protein-Serine-Threonine Kinases (métabolisme), Protéines fongiques (métabolisme), Réponse aux protéines mal repliées (MeSH), Réticulum endoplasmique (métabolisme), Saccharomycetales (croissance et développement), Saccharomycetales (métabolisme).
- MESH :
- croissance et développement : Saccharomycetales.
- génétique : Mitochondries.
- métabolisme : Mitochondries, Protein-Serine-Threonine Kinases, Protéines fongiques, Réticulum endoplasmique, Saccharomycetales.
- Réponse aux protéines mal repliées.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Fungal Proteins, Protein-Serine-Threonine Kinases.
- genetics : Mitochondria.
- growth & development : Saccharomycetales.
- metabolism : Endoplasmic Reticulum, Mitochondria, Saccharomycetales.
- Unfolded Protein Response.
Abstract
Recent findings suggest that evolutionarily distant organisms share the key features of the aging process and exhibit similar mechanisms of its modulation by certain genetic, dietary and pharmacological interventions. The scope of this review is to analyze mechanisms that in the yeast Saccharomyces cerevisiae underlie: (1) the replicative and chronological modes of aging; (2) the convergence of these 2 modes of aging into a single aging process; (3) a programmed differentiation of aging cell communities in liquid media and on solid surfaces; and (4) longevity-defining responses of cells to some chemical compounds released to an ecosystem by other organisms populating it. Based on such analysis, we conclude that all these mechanisms are programs for upholding the long-term survival of the entire yeast population inhabiting an ecological niche; however, none of these mechanisms is a "program of aging" - i.e., a program for progressing through consecutive steps of the aging process.
DOI: 10.4161/15384101.2014.965063
PubMed: 25485579
PubMed Central: PMC4614525
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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The scope of this review is to analyze mechanisms that in the yeast Saccharomyces cerevisiae underlie: (1) the replicative and chronological modes of aging; (2) the convergence of these 2 modes of aging into a single aging process; (3) a programmed differentiation of aging cell communities in liquid media and on solid surfaces; and (4) longevity-defining responses of cells to some chemical compounds released to an ecosystem by other organisms populating it. Based on such analysis, we conclude that all these mechanisms are programs for upholding the long-term survival of the entire yeast population inhabiting an ecological niche; however, none of these mechanisms is a "program of aging" - i.e., a program for progressing through consecutive steps of the aging process. </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25485579</PMID><DateCompleted><Year>2015</Year><Month>07</Month><Day>20</Day></DateCompleted><DateRevised><Year>2020</Year><Month>09</Month><Day>30</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1551-4005</ISSN><JournalIssue CitedMedium="Internet"><Volume>13</Volume><Issue>21</Issue><PubDate><Year>2014</Year></PubDate></JournalIssue><Title>Cell cycle (Georgetown, Tex.)</Title><ISOAbbreviation>Cell Cycle</ISOAbbreviation></Journal><ArticleTitle>Quasi-programmed aging of budding yeast: a trade-off between programmed processes of cell proliferation, differentiation, stress response, survival and death defines yeast lifespan.</ArticleTitle><Pagination><MedlinePgn>3336-49</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.4161/15384101.2014.965063</ELocationID><Abstract><AbstractText>Recent findings suggest that evolutionarily distant organisms share the key features of the aging process and exhibit similar mechanisms of its modulation by certain genetic, dietary and pharmacological interventions. The scope of this review is to analyze mechanisms that in the yeast Saccharomyces cerevisiae underlie: (1) the replicative and chronological modes of aging; (2) the convergence of these 2 modes of aging into a single aging process; (3) a programmed differentiation of aging cell communities in liquid media and on solid surfaces; and (4) longevity-defining responses of cells to some chemical compounds released to an ecosystem by other organisms populating it. Based on such analysis, we conclude that all these mechanisms are programs for upholding the long-term survival of the entire yeast population inhabiting an ecological niche; however, none of these mechanisms is a "program of aging" - i.e., a program for progressing through consecutive steps of the aging process. </AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Arlia-Ciommo</LastName><ForeName>Anthony</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>a Department of Biology ; Concordia University ; Montreal , QC Canada.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Piano</LastName><ForeName>Amanda</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Leonov</LastName><ForeName>Anna</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Svistkova</LastName><ForeName>Veronika</ForeName><Initials>V</Initials></Author><Author ValidYN="Y"><LastName>Titorenko</LastName><ForeName>Vladimir 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