Li ZKim HKim JPark JH2024-09-122024-09-122023-03Li Z, Kim H, Kim J, Park JH. (2023). EP400NL is involved in PD-L1 gene activation by forming a transcriptional coactivator complex.. Biochim Biophys Acta Gene Regul Mech. 1866. 1. (pp. 194889-).1874-9399https://mro.massey.ac.nz/handle/10179/71449EP400 is an ATP-dependent chromatin remodelling enzyme that regulates DNA double-strand break repair and transcription, including cMyc-dependent gene expression. We previously showed that the N-terminal domain of EP400 increases the efficacy of chemotherapeutic drugs against cancer cells. As the EP400 N-terminal-Like (EP400NL) gene resides next to the EP400 gene locus, this prompted us to investigate whether EP400NL plays a similar role in transcriptional regulation to the full-length EP400 protein. We found that EP400NL forms a human NuA4-like chromatin remodelling complex that lacks both the TIP60 histone acetyltransferase and EP400 ATPase. However, this EP400NL complex displays H2A.Z deposition activity on a chromatin template comparable to the human NuA4 complex, suggesting another associated ATPase such as BRG1 or RuvBL1/RuvBL2 catalyses the reaction. We demonstrated that the transcriptional coactivator function of EP400NL is required for serum and IFNγ-induced PD-L1 gene activation. Furthermore, transcriptome analysis indicates that EP400NL contributes to cMyc-responsive mitochondrial biogenesis. Taken together, our studies show that EP400NL plays a role as a transcription coactivator of PD-L1 gene regulation and provides a potential target to modulate cMyc functions in cancer therapy.(c) 2022 The Author/sCC BY 4.0https://creativecommons.org/licenses/by/4.0/CancerChromatin remodellingEpigeneticH2A.ZPD-L1cMycHumansAdenosine TriphosphatasesATPases Associated with Diverse Cellular ActivitiesB7-H1 AntigenCarrier ProteinsDNA HelicasesHistonesTranscription FactorsTranscriptional ActivationEP400NL is involved in PD-L1 gene activation by forming a transcriptional coactivator complexJournal article10.1016/j.bbagrm.2022.1948891876-4320journal-article194889-https://www.ncbi.nlm.nih.gov/pubmed/36328277194889S1874-9399(22)00104-3