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Understanding the Function of Mammalian Sirtuins and Protein Lysine Acylation.
Wang, Miao; Lin, Hening.
Afiliação
  • Wang M; Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA; email: hl379@cornell.edu.
  • Lin H; Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA; email: hl379@cornell.edu.
Annu Rev Biochem ; 90: 245-285, 2021 06 20.
Article em En | MEDLINE | ID: mdl-33848425
ABSTRACT
Protein lysine acetylation is an important posttranslational modification that regulates numerous biological processes. Targeting lysine acetylation regulatory factors, such as acetyltransferases, deacetylases, and acetyl-lysine recognition domains, has been shown to have potential for treating human diseases, including cancer and neurological diseases. Over the past decade, many other acyl-lysine modifications, such as succinylation, crotonylation, and long-chain fatty acylation, have also been investigated and shown to have interesting biological functions. Here, we provide an overview of the functions of different acyl-lysine modifications in mammals. We focus on lysine acetylation as it is well characterized, and principles learned from acetylation are useful for understanding the functions of other lysine acylations. We pay special attention to the sirtuins, given that the study of sirtuins has provided a great deal of information about the functions of lysine acylation. We emphasize the regulation of sirtuins to illustrate that their regulation enables cells to respond to various signals and stresses.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sirtuínas / Lisina / Mamíferos Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sirtuínas / Lisina / Mamíferos Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article