Class I histone deacetylases (HDAC1–3) are histone lysine delactylases
University of Copenhagen · University of Chicago · +1 more institution
Abstract
Lysine L-lactylation [K(L-la)] is a newly discovered histone mark stimulated under conditions of high glycolysis, such as the Warburg effect. K(L-la) is associated with functions that are different from the widely studied histone acetylation. While K(L-la) can be introduced by the acetyltransferase p300, histone delactylases enzymes remained unknown. Here, we report the systematic evaluation of zinc- and nicotinamide adenine dinucleotide–dependent histone deacetylases (HDACs) for their ability to cleave ε- N -L-lactyllysine marks. Our screens identified HDAC1–3 and SIRT1–3 as delactylases in vitro. HDAC1–3 show robust activity toward not only K(L-la) but also K(D-la) and diverse short-chain acyl modifications.…
Citation impact
- FWCI
- 47.82
- Percentile
- 100%
- References
- 76
Authors
14Topics & keywords
- Histone
- Acetylation
- Histone deacetylase 2
- Biochemistry
- Histone acetyltransferase
- Histone Acetyltransferases
- Histone methyltransferase
- Histone H2A