NKX2.2 and KLF4 cooperate to regulate α cell identity

Abstract

AbstractTranscription factors (TFs) are indispensable for maintaining cell identity through regulating cell-specific gene expression. Distinct cell identities derived from a common progenitor are frequently perpetuated by shared TFs; yet the mechanisms that enable these TFs to regulate cell-specific targets are poorly characterized. We report that the TF NKX2.2 is critical for the identity of pancreatic islet α cells by directly activating α cell genes and repressing alternate islet cell fate genes. When compared to the known role of NKX2.2 in islet β cells, we demonstrate that NKX2.2 regulates α cell genes, facilitated in part by α cell specific DNA binding at gene promoters. Furthermore, we have identified the reprogramming factor KLF4 as having enriched expression in α cells, where it co-occupies NKX2.2-bound α cell promoters, is necessary for NKX2.2 promoter occupancy in α cells and co-regulates many NKX2.2 α cell transcriptional targets. Misexpression ofKlf4in β cells is sufficient to manipulate chromatin accessibility, increase binding of NKX2.2 at α cell specific promoter sites, and alter expression of NKX2.2-regulated cell-specific targets. This study identifies KLF4 is a novel α cell factor that cooperates with NKX2.2 to regulate α cell identity.