H4K16 acylations destabilize chromatin architecture and facilitate transcriptional response during metabolic perturbations 

2025-12-19

Sandra Nitsch, Aria E. Coraor, Tamas Schauer, Yiheng Wu, Jianfeng Sun, Natalie Möritz, Jonas Funke, Harsh Nagpal, Gabriella N.L. Chua, Federica Battistini, Shannon M. Lauberth, Eva Richard, Modesto Orozco, Shixin Liu, Lourdes R. Desviat, Beat Fierz, Hendrik Dietz, Robert G. Roeder, Juan J. de Pablo, Robert Schneider

Mol Cell, 2025,  86:1-17

https://www.sciencedirect.com/science/article/pii/S1097276525009712?via%3Dihub

Histone modifications play crucial roles in genome function. However, how chromatin integrates physiological and metabolic responses at the molecular level remains largely unknown. Acetylation of histone H4 lysine 16 (H4K16ac) is unique, as it directly regulates chromatin architecture. Here, we investigated the roles of two additional H4K16 short-chain acylations, propionylation (H4K16pr) and butyrylation (H4K16bu), in chromatin architecture and transcriptional regulation. We demonstrate distinct in vitro effects of H4K16 acylations on chromatin structure, including inter- and intra-nucleosomal interactions. Utilizing a mouse model of the metabolic disease propionic acidemia, we reveal a transcriptional response concomitant with changes in H4K16 acylations in vivo. Our work suggests the importance of simultaneous action of histone acylations for transcriptional robustness through effects on nucleosomal interactions. We propose that this mode of action distinguishes H4K16 acylations from other modifications that also differ by one carbon, such as methylations.