Literature DB >> 22114328

Sirtuins, aging, and metabolism.

Leonard Guarente1.   

Abstract

Sirtuins are nicotinamide adenine dinucleotide (NAD)-dependent protein deacetylases that link protein acetylation, metabolism, aging, and diseases of aging. Sirtuins were initially found to slow aging in lower organisms and more recently shown to mediate many effects of calorie restriction on metabolism and longevity in mammals. This chapter focuses on two key mammalian sirtuins, SIRT1 (which resides mainly in the nucleus) and SIRT3 (which is mitochondrial). I discuss the many protein substrates of these sirtuins and how they determine the metabolic strategy most efficacious under scarce or abundant food supplies. I also discuss the logic by which sirtuins link protein acetylation and metabolism. Finally, I discuss emerging data showing protection by sirtuins against most of the common diseases of aging. It is possible that sirtuins will be novel targets to combat these diseases pharmacologically.

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Year:  2011        PMID: 22114328     DOI: 10.1101/sqb.2011.76.010629

Source DB:  PubMed          Journal:  Cold Spring Harb Symp Quant Biol        ISSN: 0091-7451


  87 in total

1.  Will the real aging Sirtuin please stand up?

Authors:  Chen-Yu Liao; Brian K Kennedy
Journal:  Cell Res       Date:  2012-04-17       Impact factor: 25.617

Review 2.  The place of genetics in ageing research.

Authors:  Nir Barzilai; Leonard Guarente; Thomas B L Kirkwood; Linda Partridge; Thomas A Rando; P Eline Slagboom
Journal:  Nat Rev Genet       Date:  2012-07-10       Impact factor: 53.242

3.  SIRT1-mediated deacetylation of CRABPII regulates cellular retinoic acid signaling and modulates embryonic stem cell differentiation.

Authors:  Shuang Tang; Gang Huang; Wei Fan; Yue Chen; James M Ward; Xiaojiang Xu; Qing Xu; Ashley Kang; Michael W McBurney; David C Fargo; Guang Hu; Eveline Baumgart-Vogt; Yingming Zhao; Xiaoling Li
Journal:  Mol Cell       Date:  2014-08-21       Impact factor: 17.970

4.  Mutant huntingtin inhibits the mitochondrial unfolded protein response by impairing ABCB10 mRNA stability.

Authors:  Zixing Fu; Fang Liu; Chunyue Liu; Beifang Jin; Yueqing Jiang; Mingliang Tang; Xin Qi; Xing Guo
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2019-02-23       Impact factor: 5.187

5.  Elevated microRNA-34a in obesity reduces NAD+ levels and SIRT1 activity by directly targeting NAMPT.

Authors:  Sunmi Seok; Dong-Hyun Kim; Sung-E Choi; Ting Fu; Eunkyung Yu; Kwan-Woo Lee; Yup Kang; Xiaoling Li; Byron Kemper; Jongsook Kim Kemper
Journal:  Aging Cell       Date:  2013-08-11       Impact factor: 9.304

6.  Histone Deacetylase SIRT1 Controls Proliferation, Circadian Rhythm, and Lipid Metabolism during Liver Regeneration in Mice.

Authors:  Marina Maria Bellet; Selma Masri; Giuseppe Astarita; Paolo Sassone-Corsi; Maria Agnese Della Fazia; Giuseppe Servillo
Journal:  J Biol Chem       Date:  2016-09-15       Impact factor: 5.157

7.  Histone/protein deacetylase SIRT1 is an anticancer therapeutic target.

Authors:  Bor-Jang Hwang; Amrita Madabushi; Jin Jin; Shiou-Yuh S Lin; A-Lien Lu
Journal:  Am J Cancer Res       Date:  2014-05-26       Impact factor: 6.166

Review 8.  Mitochondrial maintenance failure in aging and role of sexual dimorphism.

Authors:  John Tower
Journal:  Arch Biochem Biophys       Date:  2014-10-25       Impact factor: 4.013

Review 9.  Regulation of SIRT1 by microRNAs.

Authors:  Sung-E Choi; Jongsook Kim Kemper
Journal:  Mol Cells       Date:  2013-11-06       Impact factor: 5.034

10.  Sirtuin 3 Deregulation Promotes Pulmonary Fibrosis.

Authors:  Meredith L Sosulski; Rafael Gongora; Carol Feghali-Bostwick; Joseph A Lasky; Cecilia G Sanchez
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2017-05-01       Impact factor: 6.053

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