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Engineering longevity-design of a synthetic gene oscillator to slow cellular aging.
Zhou, Zhen; Liu, Yuting; Feng, Yushen; Klepin, Stephen; Tsimring, Lev S; Pillus, Lorraine; Hasty, Jeff; Hao, Nan.
Afiliación
  • Zhou Z; Department of Molecular Biology, University of California San Diego, La Jolla, CA 92093, USA.
  • Liu Y; Department of Molecular Biology, University of California San Diego, La Jolla, CA 92093, USA.
  • Feng Y; Department of Molecular Biology, University of California San Diego, La Jolla, CA 92093, USA.
  • Klepin S; Department of Molecular Biology, University of California San Diego, La Jolla, CA 92093, USA.
  • Tsimring LS; Synthetic Biology Institute, University of California San Diego, La Jolla, CA 92093, USA.
  • Pillus L; Department of Molecular Biology, University of California San Diego, La Jolla, CA 92093, USA.
  • Hasty J; UCSD Moores Cancer Center, University of California San Diego, La Jolla, CA 92093, USA.
  • Hao N; Department of Molecular Biology, University of California San Diego, La Jolla, CA 92093, USA.
Science ; 380(6643): 376-381, 2023 04 28.
Article en En | MEDLINE | ID: mdl-37104589
ABSTRACT
Synthetic biology enables the design of gene networks to confer specific biological functions, yet it remains a challenge to rationally engineer a biological trait as complex as longevity. A naturally occurring toggle switch underlies fate decisions toward either nucleolar or mitochondrial decline during the aging of yeast cells. We rewired this endogenous toggle to engineer an autonomous genetic clock that generates sustained oscillations between the nucleolar and mitochondrial aging processes in individual cells. These oscillations increased cellular life span through the delay of the commitment to aging that resulted from either the loss of chromatin silencing or the depletion of heme. Our results establish a connection between gene network architecture and cellular longevity that could lead to rationally designed gene circuits that slow aging.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Senescencia Celular / Genes Sintéticos / Longevidad Tipo de estudio: Prognostic_studies Idioma: En Revista: Science Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Senescencia Celular / Genes Sintéticos / Longevidad Tipo de estudio: Prognostic_studies Idioma: En Revista: Science Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos