Activation of the Protein Deacetylase SIRT6 by Long-chain Fatty Acids and Widespread Deacylation by Mammalian Sirtuins
University of Wisconsin–Madison · Wisconsin Institutes for Discovery
Abstract
Mammalian sirtuins (SIRT1 through SIRT7) are members of a highly conserved family of NAD(+)-dependent protein deacetylases that function in metabolism, genome maintenance, and stress responses. Emerging evidence suggests that some sirtuins display substrate specificity toward other acyl groups attached to the lysine ε-amine. SIRT6 was recently reported to preferentially hydrolyze long-chain fatty acyl groups over acetyl groups. Here we investigated the catalytic ability of all sirtuins to hydrolyze 13 different acyl groups from histone H3 peptides, ranging in carbon length, saturation, and chemical diversity. We find that long-chain deacylation is a general feature of mammalian sirtuins, that SIRT1 and SIRT2…
Citation impact
- FWCI
- 27.89
- Percentile
- 100%
- References
- 38
Authors
3Topics & keywords
- Sirtuin
- SIRT2
- Biochemistry
- SIRT3
- Acetylation
- Myristoylation
- NAD+ kinase
- Biology