@article {Moreno-Yruela211839, author = {Carlos Moreno-Yruela and Iacopo Galleano and Andreas S. Madsen and Christian A. Olsen}, title = {Histone Deacetylase 11 is an ε-N-Myristoyllysine Hydrolase}, elocation-id = {211839}, year = {2017}, doi = {10.1101/211839}, publisher = {Cold Spring Harbor Laboratory}, abstract = {Histone deacetylase (HDAC) enzymes are important regulators of diverse biological function, including gene expression, rendering them potential targets for intervention in a number of diseases, with a handful of compounds approved for treatment of certain hematologic cancers. Among the human zinc-dependent HDACs, the most recently discovered member, HDAC11, is the only member assigned to subclass IV, the smallest protein, and the least well understood with regards to biological function. Here we show that HDAC11 cleaves long chain acyl modifications on lysine side chains with remarkable efficiency compared to acetyl groups. We further show that several common types of HDAC inhibitors, including the approved drugs romidepsin and vorinostat, do not inhibit this enzymatic activity. Macrocyclic hydroxamic acid-containing peptides, on the other hand, potently inhibit HDAC11 demyristoylation activity. These findings should be taken carefully into consideration in future investigations of the biological function of HDAC11 and will serve as a foundation for the development of selective chemical probes targeting HDAC11.}, URL = {https://www.biorxiv.org/content/early/2017/11/01/211839}, eprint = {https://www.biorxiv.org/content/early/2017/11/01/211839.full.pdf}, journal = {bioRxiv} }