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      Function and regulation of the mitochondrial Sirtuin isoform Sirt5 in Mammalia

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      Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics
      Elsevier BV

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          Abstract

          Sirtuins are a family of protein deacetylases that catalyze the nicotinamide adenine dinucleotide (NAD(+))-dependent removal of acetyl groups from modified lysine side chains in various proteins. Sirtuins act as metabolic sensors and influence metabolic adaptation but also many other processes such as stress response mechanisms, gene expression, and organismal aging. Mammals have seven Sirtuin isoforms, three of them - Sirt3, Sirt4, and Sirt5 - located to mitochondria, our centers of energy metabolism and apoptosis initiation. In this review, we shortly introduce the mammalian Sirtuin family, with a focus on the mitochondrial isoforms. We then discuss in detail the current knowledge on the mitochondrial isoform Sirt5. Its physiological role in metabolic regulation has recently been confirmed, whereas an additional function in apoptosis regulation remains speculative. We will discuss the biochemical properties of Sirt5 and how they might contribute to its physiological function. Furthermore, we discuss the potential use of Sirt5 as a drug target, structural features of Sirt5 and of an Sirt5/inhibitor complex as well as their differences to other Sirtuins and the current status of modulating Sirt5 activity with pharmacological compounds. Copyright 2009 Elsevier B.V. All rights reserved.

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          Author and article information

          Journal
          Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics
          Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics
          Elsevier BV
          15709639
          August 2010
          August 2010
          : 1804
          : 8
          : 1658-1665
          Article
          10.1016/j.bbapap.2009.09.011
          19766741
          db764be1-a40e-47e9-a198-0bde849296a0
          © 2010

          https://www.elsevier.com/tdm/userlicense/1.0/

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