MRG15 orchestrates rhythmic epigenomic remodelling and controls hepatic lipid metabolism

The rhythmic regulation of transcriptional processes is intimately linked to lipid homeostasis, to anticipate daily changes in energy access. The Rev-erbα–HDAC3 complex was previously discovered to execute the rhythmic repression of lipid genes; however, the epigenetic switch that turns on these genes is less clear. Here, we show that genomic recruitment of MRG15, which is encoded by the mortality factor on chromosome 4 ( MORF4 )-related gene on chromosome 15, displays a significant diurnal rhythm and activates lipid genes in the mouse liver. RNA polymerase II (Pol II) recruitment and histone acetylation correspond to MRG15 binding, and the rhythm is impaired upon MRG15 depletion, establishing MRG15 as a key modulator in global rhythmic transcriptional regulation. MRG15 interacts with the nuclear receptor LRH-1, rather than with known core clock proteins, and is recruited to genomic loci near lipid genes via LRH-1. Blocking of MRG15 by CRISPR targeting or by the FDA-approved drug argatroban, which is an antagonist to MRG15, attenuates liver steatosis. This work highlights MRG15 as a targetable master regulator in the rhythmic regulation of hepatic lipid metabolism. Wei et al. show that the chromatin regulator MRG15 interacts with the nuclear receptor LRH-1 and is rhythmically recruited to lipid- and cholesterol-biosynthetic genes. In a nutrient-rich state, MRG15 alters histone acetylation status to activate gene transcription and lipid synthesis, whereas in a nutrient-scarce state, MRG15 genomic recruitment and lipid synthesis are reduced.